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University of California – Irvine
1.
Gallent, Erin Ann.
Approaches to promoting mTOR-mediated growth and regeneration in the mature central nervous system.
Degree: Biomedical Sciences, 2018, University of California – Irvine
URL: http://www.escholarship.org/uc/item/98c4k608
► Regeneration of the injured adult central nervous system is limited. The phosphatase and tensin homolog on chromosome ten (PTEN) gene has been shown to enable…
(more)
▼ Regeneration of the injured adult central nervous system is limited. The phosphatase and tensin homolog on chromosome ten (PTEN) gene has been shown to enable axonal regeneration in optic nerve crush and spinal cord injury models following neonatal conditional genetic deletion of PTEN (Park et al., 2008; Liu et al., 2010). As a follow-up to these experiments, I assessed the long-term histological and behavioral consequences of neonatal PTEN deletion (Gutilla et al., 2016). In this study, I observed massive cell body enlargement of the neurons that give rise to the major descending voluntary motor tract in the spinal cord (called cortical motoneurons, or CMNs). This discovery led us to hypothesize that deletion of PTEN during adulthood would also result in neuronal growth. Using two-photon microscopy and electron microscopy I found that adult PTEN deletion in neurons results in significant cell body and axonal growth, and that these enlarged neurons continue to express markers of growth-promoting pathways throughout life. To gain a better understanding of the morphological consequences of PTEN deletion in adult neurons, I imaged thick sections (200µm) containing fluorescently labeled PTEN deleted and control neurons in 3D using a modified CLARITY protocol and two-photon microscopy (Chung and Deisseroth, 2013). 3D images were then used to generate 2D projections that were processed using Sholl analysis, or concentric circle analysis (Sholl, 1953). We found that at both 6 and 12 months post-PTEN deletion, pyramidal neurons have a significantly higher density of dendrites, and that this increase is significant at the largest number of radii away from the soma at 12 months after deletion. The progressive changes in dendritic morphology were also seen in the number of basal dendrites projecting off of the soma number, maximal dendritic projections, and nodes, with the highest values for all three measurements seen at 12 months, not 6 months, post-deletion. What’s more, the radius of maximal intersection for pyramidal neurons is normally between 60-80 µm away from the soma. Only at 12 months post-deletion did pyramidal neurons exhibit a shift in the radius of maximal intersection, indicating that as PTEN deletion-induced changes in morphology progress over time, neurons becomes increasingly abnormal compared to controls.To assess the effect of adult PTEN deletion on neuronal function and behavior, I performed behavioral assessments of forelimb motor function at 2 month intervals following induction of adult PTEN deletion. Using the rotarod task to measure baseline coordination and motor learning, and the cylinder task to identify asymmetry in spontaneous forelimb exploration, I found significant improvement in baseline coordination and motor learning beginning at 8 months after PTEN deletion, and spared symmetry of forelimb exploration at all assessed time points. Pulling our structural and functional data together, the timing of functional improvement onset correlates with the progressive development of increased dendritic…
Subjects/Keywords: Neurosciences; Anatomy and Neurobiology
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APA (6th Edition):
Gallent, E. A. (2018). Approaches to promoting mTOR-mediated growth and regeneration in the mature central nervous system. (Thesis). University of California – Irvine. Retrieved from http://www.escholarship.org/uc/item/98c4k608
Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
Chicago Manual of Style (16th Edition):
Gallent, Erin Ann. “Approaches to promoting mTOR-mediated growth and regeneration in the mature central nervous system.” 2018. Thesis, University of California – Irvine. Accessed December 06, 2019.
http://www.escholarship.org/uc/item/98c4k608.
Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
MLA Handbook (7th Edition):
Gallent, Erin Ann. “Approaches to promoting mTOR-mediated growth and regeneration in the mature central nervous system.” 2018. Web. 06 Dec 2019.
Vancouver:
Gallent EA. Approaches to promoting mTOR-mediated growth and regeneration in the mature central nervous system. [Internet] [Thesis]. University of California – Irvine; 2018. [cited 2019 Dec 06].
Available from: http://www.escholarship.org/uc/item/98c4k608.
Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
Council of Science Editors:
Gallent EA. Approaches to promoting mTOR-mediated growth and regeneration in the mature central nervous system. [Thesis]. University of California – Irvine; 2018. Available from: http://www.escholarship.org/uc/item/98c4k608
Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

University of California – Irvine
2.
Karsten, Carley.
Mapping brain networks engaged by spaced learning.
Degree: Biomedical Sciences, 2017, University of California – Irvine
URL: http://www.escholarship.org/uc/item/0517c8p3
► Spaced training is a powerful behavioral method for enhancing long-term memory. Despite decades of observational study of this phenomenon, a precise neurobiological mechanism remains unknown.…
(more)
▼ Spaced training is a powerful behavioral method for enhancing long-term memory. Despite decades of observational study of this phenomenon, a precise neurobiological mechanism remains unknown. Memory consolidation literature describes both synaptic and systems-level changes that accompany the stabilization of memory traces; the aim of the present work was to determine at which level spaced training operates. A specific spaced training schedule in the object location memory (OLM) task has been shown to dramatically lower the threshold to long-term memory in mice. Here we compare this paradigm to the standard, single-trial, “massed” schedule of training on a number of neurobiological outcomes. First we assayed, across the entire mouse brain, patterns of neuronal activation as reflected by Fos immunoreactivity. This analysis revealed a distinct network difference between spaced and massed training; specifically, the orbitofrontal cortex (OFC) showed significantly different activity. Next we chemogenetically inactivated OFC during massed and spaced training and found that it was necessary for spaced, but not massed, OLM learning. In Chapter 3 we assayed patterns of synaptic modification in hippocampus after massed and spaced OLM training. This analysis did not significantly distinguish between the training schedules. The studies in Chapters 4 and 5 depart from the spaced vs. massed question, and instead venture into territory of intellectual disability. The Fmr1-KO mouse is a commonly-used model of Fragile-X Syndrome, the most common form of inherited intellectual disability in humans. Here we show that these mice fail to exhibit social recognition, and that this deficit is corrected with treatments which enhance TrkB signaling. In Chapter 5, we apply behavioral pattern analysis (Markov sequences) to WT vs. KO exploratory patterns, and then to behavioral tasks discussed in Chapters 1-3 (including spaced vs. massed training and OFC inactivation). The main takeaway of this ethological analysis was that exploratory patterns vary more with environmental novelty than with any other factor. Together the studies in this dissertation support a systems-level effect of spaced training upon long-term memory, which may or may not be related to the difference in exploratory movement patterns.
Subjects/Keywords: Neurosciences; anatomy; hippocampus; memory; spaced training
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MLA ·
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APA (6th Edition):
Karsten, C. (2017). Mapping brain networks engaged by spaced learning. (Thesis). University of California – Irvine. Retrieved from http://www.escholarship.org/uc/item/0517c8p3
Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
Chicago Manual of Style (16th Edition):
Karsten, Carley. “Mapping brain networks engaged by spaced learning.” 2017. Thesis, University of California – Irvine. Accessed December 06, 2019.
http://www.escholarship.org/uc/item/0517c8p3.
Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
MLA Handbook (7th Edition):
Karsten, Carley. “Mapping brain networks engaged by spaced learning.” 2017. Web. 06 Dec 2019.
Vancouver:
Karsten C. Mapping brain networks engaged by spaced learning. [Internet] [Thesis]. University of California – Irvine; 2017. [cited 2019 Dec 06].
Available from: http://www.escholarship.org/uc/item/0517c8p3.
Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
Council of Science Editors:
Karsten C. Mapping brain networks engaged by spaced learning. [Thesis]. University of California – Irvine; 2017. Available from: http://www.escholarship.org/uc/item/0517c8p3
Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Stellenbosch University
3.
Mazyala, Eric John.
A morphological study of the dermal fibroblast.
Degree: MScMedSc (Biomedical Sciences. Anatomy and Histology, Biomedical Sciences, 2008, Stellenbosch University
URL: http://hdl.handle.net/10019.1/4079
Subjects/Keywords: Anatomy and histology
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❌
APA ·
Chicago ·
MLA ·
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APA (6th Edition):
Mazyala, E. J. (2008). A morphological study of the dermal fibroblast. (Masters Thesis). Stellenbosch University. Retrieved from http://hdl.handle.net/10019.1/4079
Chicago Manual of Style (16th Edition):
Mazyala, Eric John. “A morphological study of the dermal fibroblast.” 2008. Masters Thesis, Stellenbosch University. Accessed December 06, 2019.
http://hdl.handle.net/10019.1/4079.
MLA Handbook (7th Edition):
Mazyala, Eric John. “A morphological study of the dermal fibroblast.” 2008. Web. 06 Dec 2019.
Vancouver:
Mazyala EJ. A morphological study of the dermal fibroblast. [Internet] [Masters thesis]. Stellenbosch University; 2008. [cited 2019 Dec 06].
Available from: http://hdl.handle.net/10019.1/4079.
Council of Science Editors:
Mazyala EJ. A morphological study of the dermal fibroblast. [Masters Thesis]. Stellenbosch University; 2008. Available from: http://hdl.handle.net/10019.1/4079

Stellenbosch University
4.
Page, Benedict J. (Benedict John).
A histological and morphometric assessment of endocrine and ductular proliferation in the adult rat pancreas using an occlusive pancreatic duct ligation model.
Degree: PhD, Biomedical Sciences, 2000, Stellenbosch University
URL: http://hdl.handle.net/10019.1/51573
► ENGLISH ABSTRACT: Diabetes Mellitus (DM) is synonymous with "B-cell failure". Ligation of the pancreatic duct distally to its confluence into the bile duct has been…
(more)
▼ ENGLISH ABSTRACT: Diabetes Mellitus (DM) is synonymous with "B-cell failure". Ligation of the pancreatic
duct distally to its confluence into the bile duct has been shown to induce endocrine
tissue regeneration from a number of probable sources. The cells responsible for
regeneration are supposed to possess either dormant pluripotent stem cell ability and/or
the plasticity to undergo metaplasia to form new and surplus endocrine tissue able to
replace pathologically and/or experimentally compromised pancreas. The sequence of
events (cell lineage) during this process of neogenesis, has been the source of
controversy for quite some time as various studies suggest that the cell lineage differs
from in vivo and in vitro studies, according to experimental model and species of
laboratory animal.
The object of this study was to utilise an established experimental laboratory animal
model to study islet morphological changes, neogenesis and or both in vivo. Further
aims of the study were to determine the extent, sequence and magnitude of pancreatic
duct ligation (PDL) induced endocrine neogenesis/morphogenesis in a laboratory rat
model using occlusive pancreatic duct ligation.
PDL's were performed on six groups of 25 normal adult Sprague-Dawley (SD) rats
(300g+) according to the method of Hultquist and Jonsson (1965). Experimental
animals were sacrificed at 12 hr intervals from day one post-PDL to day 10 and every
24 hrs thereafter to day 14 as described by Wang, Klëppel, Bouwens (1995). Animals
received BrdU (a thymidine marker and cell proliferation indicator) 50mglkg
intraperitoneally as described by Wang et al. (1995), one hour prior to removal of the
pancreas after which it was fixed in Bouin's solution and histologically processed.
Seven consecutive 3-6 urn thick serial sections were sequentially stained with H & E,
insulin (I), glucagon (G), somatostatin (ST), pancreatic polypeptide (PP), neuropeptide
tyrosine (NPY) and peptide tyrosine tyrosine (PYY). Immunolabeling was done
according to the method of Guesdon, Temynck , Avrameas (1979). Double
immunolabeling for BrdU and each pancreatic peptide was performed on the sections
on days 3,5, 7, 9 and 11 as described by Wang et al (1994). Cellular transformation between one and 3Yz days was characterised by simultaneous
total deletion and/or transdifferentiation of the acinar compartment and the appearance
of immunoreactive cells for I (11.53 ±1.5%), G (1.85 ±0.8%), pp (1.50 ±0.09%), and
ST (1.96 ±0.24%). Changes in the endocrine composition in existing islets, occurred
along a pathway that saw PP- and ST-cells invading the islet core, islet mantle glucagon
deletion and random appearance of all endocrine cell types within the inter-islet
interstitium on day 3Yz. Days 4 to 6Yz saw further endocrine expansion while days 7 to
14 were distinguished by islet reconstitution and consolidation. NPY immunoreactivity
appeared on day 4Y2 and persisted intermittently throughout while PVV first appeared
on day 4 and disappeared after day 7Yz.
The…
Advisors/Committee Members: Du Toit, Don F., Wolfe-coote, Sonia A., Stellenbosch University. Faculty of Medicine & Health Science. Dept. of Biomedical Sciences..
Subjects/Keywords: Anatomy and histology
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❌
APA ·
Chicago ·
MLA ·
Vancouver ·
CSE |
Export
to Zotero / EndNote / Reference
Manager
APA (6th Edition):
Page, B. J. (. J. (2000). A histological and morphometric assessment of endocrine and ductular proliferation in the adult rat pancreas using an occlusive pancreatic duct ligation model. (Doctoral Dissertation). Stellenbosch University. Retrieved from http://hdl.handle.net/10019.1/51573
Chicago Manual of Style (16th Edition):
Page, Benedict J (Benedict John). “A histological and morphometric assessment of endocrine and ductular proliferation in the adult rat pancreas using an occlusive pancreatic duct ligation model.” 2000. Doctoral Dissertation, Stellenbosch University. Accessed December 06, 2019.
http://hdl.handle.net/10019.1/51573.
MLA Handbook (7th Edition):
Page, Benedict J (Benedict John). “A histological and morphometric assessment of endocrine and ductular proliferation in the adult rat pancreas using an occlusive pancreatic duct ligation model.” 2000. Web. 06 Dec 2019.
Vancouver:
Page BJ(J. A histological and morphometric assessment of endocrine and ductular proliferation in the adult rat pancreas using an occlusive pancreatic duct ligation model. [Internet] [Doctoral dissertation]. Stellenbosch University; 2000. [cited 2019 Dec 06].
Available from: http://hdl.handle.net/10019.1/51573.
Council of Science Editors:
Page BJ(J. A histological and morphometric assessment of endocrine and ductular proliferation in the adult rat pancreas using an occlusive pancreatic duct ligation model. [Doctoral Dissertation]. Stellenbosch University; 2000. Available from: http://hdl.handle.net/10019.1/51573

Stellenbosch University
5.
Tchokonte-Nana, Venant.
Cellular mechanisms involved in the recapitulation of endocrine development in the duct ligated pancreas.
Degree: PhD, Biomedical Sciences, 2011, Stellenbosch University
URL: http://hdl.handle.net/10019.1/6828
► ENGLISH ABSTRACT: Diabetes mellitus is amongst the leading causes of morbidity and mortality in the world, affecting young, adult and old people. Beta cell replacement…
(more)
▼ ENGLISH ABSTRACT: Diabetes mellitus is amongst the leading causes of morbidity and mortality in the world, affecting
young, adult and old people. Beta cell replacement therapy for insulin delivery remains the ultimate
remedy for diabetes. However, insufficient donor pancreas and the use of immunosuppressive drugs
prevent the wide-spread of this therapy. Other avenues of self generated beta cells within the organ
itself need to be explored. Therefore, understanding the chronobiology of cellular mechanisms in
the lineage of beta cell induced neogenesis is a valuable tool in improving beta cell replacement in
patients with diabetes. The aim of this study was to induce recapitulation of the morpho-genetic
sequence of endocrine cells development in the pancreas of rats after the pancreatic duct ligation
(PDL) procedure. Serial sections of PDL tissues of the pancreas were obtained from 78 Sprague-
Dawley rats and were assessed morphologically. The immunofluorescent tissues were statistically
analysed using a computerized morphometry technique. The protein expression indices of
Caspase3, Insulin, Pdx1, Ngn3, NeuroD and Pax6 were quantified. The efficiency levels of coexpression
of these homeodomain proteins separately with insulin were defined by the ratio of the
mean value of insulin expression to the mean value of their respective protein expression. The
morphological changes were characterized by the appearance of granulated acinar cells at 6 hours
post-PDL and the proliferation of endocrine tissues from 84 hours through to 120 hours. The
morpho-immunofluorescent evaluation showed the highest immunoreactivity of Caspase3 and Pdx1
at 6 hours, Ngn3 at 36 hours, Pax6 and insulin at 84 hours while NeuroD expression was at 120
hours. The immunohistofluorescent analysis showed that caspase3 and Pdx1 were the first to be
expressed at 6 hours while the insulin and NeuroD expression appeared later at 84 hours and 120
hours, respectively. However, Pax6 expression was continuous across time periods post-PDL, while
Ngn3 expression showed a peak at 36 hours. The efficiency (highest and earliest expression) of co-expression of all these homeodomain proteins with insulin was restricted between 12 hours and 24
hours. The optimal efficiency was at 12 hours by Ngn3 with insulin. A good efficiency was shown
for Pdx1 with insulin, NeuroD with insulin and Pax6 with insulin at 12 hours and 24 hours,
respectively. A low efficiency was observed for insulin and caspase3 co-expression at 24 hours.
This study suggests that for transplantation, PDL tissues harvested at an early time post-PDL
(between 12 and 24 hours) could yield a higher success rate; the study also provides evidence for a
connection between morphological changes in the PDL pancreas and the protein synthesis
necessary for the lineage of endocrine cell development.
AFRIKAANSE OPSOMMING: Diabetes Mellitus resorteer onder die vernaamste oorsake van morbiditeit en mortaliteit wêreldwyd,
en tuister jongmense, volwassenes en bejaardes. Daar bestaan egter…
Advisors/Committee Members: Page, Benedict J., Du Toit, Don F., University of Stellenbosch. Faculty of Health Sciences. Dept. of Biomedical Sciences. Anatomy and Histology..
Subjects/Keywords: Histology; Dissertations – Anatomy; Dissertations – Histology; Endocrine cell development; Biomedical Sciences. Anatomy and Histology
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❌
APA ·
Chicago ·
MLA ·
Vancouver ·
CSE |
Export
to Zotero / EndNote / Reference
Manager
APA (6th Edition):
Tchokonte-Nana, V. (2011). Cellular mechanisms involved in the recapitulation of endocrine development in the duct ligated pancreas. (Doctoral Dissertation). Stellenbosch University. Retrieved from http://hdl.handle.net/10019.1/6828
Chicago Manual of Style (16th Edition):
Tchokonte-Nana, Venant. “Cellular mechanisms involved in the recapitulation of endocrine development in the duct ligated pancreas.” 2011. Doctoral Dissertation, Stellenbosch University. Accessed December 06, 2019.
http://hdl.handle.net/10019.1/6828.
MLA Handbook (7th Edition):
Tchokonte-Nana, Venant. “Cellular mechanisms involved in the recapitulation of endocrine development in the duct ligated pancreas.” 2011. Web. 06 Dec 2019.
Vancouver:
Tchokonte-Nana V. Cellular mechanisms involved in the recapitulation of endocrine development in the duct ligated pancreas. [Internet] [Doctoral dissertation]. Stellenbosch University; 2011. [cited 2019 Dec 06].
Available from: http://hdl.handle.net/10019.1/6828.
Council of Science Editors:
Tchokonte-Nana V. Cellular mechanisms involved in the recapitulation of endocrine development in the duct ligated pancreas. [Doctoral Dissertation]. Stellenbosch University; 2011. Available from: http://hdl.handle.net/10019.1/6828

East Tennessee State University
6.
Kim, Jong G.
Cytokines and Ovulation in the Mouse Ovary.
Degree: PhD, Biomedical Sciences, 1994, East Tennessee State University
URL: https://dc.etsu.edu/etd/2711
► Ovulation has been hypothesized as an inflammatory process. Interleukin(IL)-1α, IL-1β and tumor necrosis factor(TNF)-α are potent cytokines produced from macrophages and various other cell…
(more)
▼ Ovulation has been hypothesized as an inflammatory process. Interleukin(IL)-1α, IL-1β and tumor necrosis factor(TNF)-α are potent cytokines produced from macrophages and various other cell types, and are pivotal components of inflammation. Although previous studies have investigated cytokine activities in the reproductive system, there is little information on their precise localization and activities during the periovulatory period. To investigate the role of cytokines in ovulation, experiments were designed to determine the immunohistochemical localization and time specific production of cytokines IL-1 and TNF-α using a mouse model at 36h, 12h, 6h, 2h before ovulation, and at 6h and 18h after ovulation in vivo. Isolated individual follicles in vitro were used to determine more precise roles of cytokines on follicular development, ovulation and steroidogenesis. From these studies it was found that (1) granulosa cells were the primary sites of IL-1α and TNF-α production from large antral follicles and preovulatory follicles in vivo, (2) production of IL-1α and TNF-α increased as ovulation neared, first appearing in the cumulus cells and expanding to antral and mural granulosa cells, (3) less intense staining of these cytokines in the theca layer of smaller follicles suggests that theca cells may contribute to the production of these cytokines to some extent, (4) but there was no IL-1β production, (5) localized and temporal production of cytokines during the periovulatory period suggests precise regulation, (6) decrease of IL-1α in the ovary after gonadotropin injection determined by enzyme linked immunoadsorbent assay suggests that IL-1α production may be under the control of gonadotropins, (7) in follicle culture without bone marrow derived cells, granulosa cells were confirmed as the main source of cytokine production, (8) addition of IL-1α and TNF-α to follicles in culture tend to decrease estradiol production. In conclusion, immunoreactive cytokine production correlated positively with the periovulatory follicular development suggesting their role as ovulatory mediators. It requires further studies on what are the signals for the initiation and termination of cytokine production, how transcription and translation of these cytokines are regulated during the periovulatory period, and how they contribute to the ovulation.
Subjects/Keywords: Anatomy and physiology; Animals; Biological sciences; Anatomy; Animal Structures
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APA ·
Chicago ·
MLA ·
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APA (6th Edition):
Kim, J. G. (1994). Cytokines and Ovulation in the Mouse Ovary. (Doctoral Dissertation). East Tennessee State University. Retrieved from https://dc.etsu.edu/etd/2711
Chicago Manual of Style (16th Edition):
Kim, Jong G. “Cytokines and Ovulation in the Mouse Ovary.” 1994. Doctoral Dissertation, East Tennessee State University. Accessed December 06, 2019.
https://dc.etsu.edu/etd/2711.
MLA Handbook (7th Edition):
Kim, Jong G. “Cytokines and Ovulation in the Mouse Ovary.” 1994. Web. 06 Dec 2019.
Vancouver:
Kim JG. Cytokines and Ovulation in the Mouse Ovary. [Internet] [Doctoral dissertation]. East Tennessee State University; 1994. [cited 2019 Dec 06].
Available from: https://dc.etsu.edu/etd/2711.
Council of Science Editors:
Kim JG. Cytokines and Ovulation in the Mouse Ovary. [Doctoral Dissertation]. East Tennessee State University; 1994. Available from: https://dc.etsu.edu/etd/2711

East Tennessee State University
7.
Lindsay, Gregory W.
Enhanced Renal Sympathetic and Cardiovascular Responses to Substance P in Hypertension.
Degree: PhD, Biomedical Sciences, 1993, East Tennessee State University
URL: https://dc.etsu.edu/etd/2718
► Blood pressure, heart rate, and renal sympathetic nerve responses were measured in 9-13 week old male spontaneously hypertensive rats (SHR) and compared to those…
(more)
▼ Blood pressure, heart rate, and renal sympathetic nerve responses were measured in 9-13 week old male spontaneously hypertensive rats (SHR) and compared to those in age and sex-matched Wistar-Kyoto (WKY) rats following intravenous injection of the neuropeptide substance P (SP), the nicotinic stimulant 1,1-dimethyl-4-phenylpiperazinium (DMPP), and the adrenoceptor stimulant norepinephrine (NE). Charles River Sprague-Dawley (CD) rats were used in some studies to develop methodologies. Measurements were made in control rats and also following sinoaortic denervation, pithing, ganglion blockade, or adrenoceptor blockade. Responses were evaluated in order to determine if ganglion stimulation by SP was enhanced in SHR compared to WKY rats and if this enhancement was selective for SP or would also be exhibited to DMPP. NE was used to evaluate adrenergic sensitivity and to confirm the success of baroreceptor denervations. SHR exhibited greater intrinsic sympathetic tone than WKY rats before and following ganglion blockade. Ganglion stimulation by SP and DMPP was only fully revealed following elimination of baroreceptor input. Results indicated that SP stimulates sympathetic ganglia to increase renal sympathetic nerve activity, heart rate and blood pressure in CD, SHR and WKY rats. This increase was enhanced in SHR compared to WKY rats in the absence of a similar enhancement of responses to DMPP. The action of SP to cause vasodilation was attenuated in SHR versus WKY rats which may augment its action as a pressor agent in SHR. In conclusion, increases in blood pressure, heart rate and renal sympathetic nerve activity were selectively increased to SP in SHR versus WKY rats. This enhanced action of SP may contribute to the elevation of basal and/or evoked sympathetic discharge observed in this model of hypertension.
Subjects/Keywords: Anatomy and physiology; Animals; Biological sciences; Anatomy; Animal Structures
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APA ·
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APA (6th Edition):
Lindsay, G. W. (1993). Enhanced Renal Sympathetic and Cardiovascular Responses to Substance P in Hypertension. (Doctoral Dissertation). East Tennessee State University. Retrieved from https://dc.etsu.edu/etd/2718
Chicago Manual of Style (16th Edition):
Lindsay, Gregory W. “Enhanced Renal Sympathetic and Cardiovascular Responses to Substance P in Hypertension.” 1993. Doctoral Dissertation, East Tennessee State University. Accessed December 06, 2019.
https://dc.etsu.edu/etd/2718.
MLA Handbook (7th Edition):
Lindsay, Gregory W. “Enhanced Renal Sympathetic and Cardiovascular Responses to Substance P in Hypertension.” 1993. Web. 06 Dec 2019.
Vancouver:
Lindsay GW. Enhanced Renal Sympathetic and Cardiovascular Responses to Substance P in Hypertension. [Internet] [Doctoral dissertation]. East Tennessee State University; 1993. [cited 2019 Dec 06].
Available from: https://dc.etsu.edu/etd/2718.
Council of Science Editors:
Lindsay GW. Enhanced Renal Sympathetic and Cardiovascular Responses to Substance P in Hypertension. [Doctoral Dissertation]. East Tennessee State University; 1993. Available from: https://dc.etsu.edu/etd/2718

East Tennessee State University
8.
Sanders, Theresa A.
Quantitation of Teratogenic Effects of 5-fluorouracil Administered to Mice in Vivo or in Submerged Limb Culture.
Degree: PhD, Biomedical Sciences, 1987, East Tennessee State University
URL: https://dc.etsu.edu/etd/2786
► This study demonstrates the use of submerged limb culture in teratologic testing. Pregnant mice were treated on day 11 of gestation (E11, plug date…
(more)
▼ This study demonstrates the use of submerged limb culture in teratologic testing. Pregnant mice were treated on day 11 of gestation (E11, plug date = E0) with 10, 20 or 40 mg of 5-fluorouracil (FU) per kg body weight. On E17, treated and untreated fetuses were examined for gross malformations and were fixed in 95% ethanol. Reduction of limb size and digital defects, including ectrodactyly (ED), syndactyly (SD), microdactyly and polydactyly were dose-dependent. In parallel studies, pregnant mice were treated on the morning of E11 and embryos were removed either 7h (E11) or 24h (E12) later for submerged limb culture. Changes in limb area showed a dose-response relationship while treatment had little effect on the shape of individual bones. This indicates the relatively unspecific nature of FU-induced embryotoxicity. E11 studies revealed a dose dependent response of ED, SD and fusion of the metacarpals/metatarsals (MC/MT) to the proximal phalanges. Unlike E11 cultures, middle phalanges were present but decreased in number as dosage increased. Limbs from embryos of untreated females were cultured (E11) in the presence of 0.002, 0.02, 0.2 or 2.0 mg FU/ml culture medium. The percentage of limbs void of paw cartilage or with decreased numbers of MC/MT was dose-dependent. A dose-dependent decrease in the deleterious effects of 0.02 mg FU/ml was observed when 0.2 or 0.02 mg thymine/ml was added to the cultures. In both culture and non-culture studies, hindlimbs (HL) were more affected than forelimbs (FL) and distal regions were more affected than proximal ones. In addition to the morphometric analyses, biochemical parameters of growth and differentiation were examined at 0, 36 and 72h of culture in untreated and treated limbs. Both DNA and protein of FU treated limbs were decreased compared to untreated controls. FL demonstrated greater capacity for regulation of losses in protein content, HL for DNA content. Submerged limb culture provides a useful model for the examination of xenobiotic effects on limb development and allows some comparative evaluation among in vivo, in vivo/in vitro and in vitro studies. (Abstract shortened with permission of author.)
Subjects/Keywords: Anatomy and physiology; Biological sciences; Anatomy; Physiology
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APA (6th Edition):
Sanders, T. A. (1987). Quantitation of Teratogenic Effects of 5-fluorouracil Administered to Mice in Vivo or in Submerged Limb Culture. (Doctoral Dissertation). East Tennessee State University. Retrieved from https://dc.etsu.edu/etd/2786
Chicago Manual of Style (16th Edition):
Sanders, Theresa A. “Quantitation of Teratogenic Effects of 5-fluorouracil Administered to Mice in Vivo or in Submerged Limb Culture.” 1987. Doctoral Dissertation, East Tennessee State University. Accessed December 06, 2019.
https://dc.etsu.edu/etd/2786.
MLA Handbook (7th Edition):
Sanders, Theresa A. “Quantitation of Teratogenic Effects of 5-fluorouracil Administered to Mice in Vivo or in Submerged Limb Culture.” 1987. Web. 06 Dec 2019.
Vancouver:
Sanders TA. Quantitation of Teratogenic Effects of 5-fluorouracil Administered to Mice in Vivo or in Submerged Limb Culture. [Internet] [Doctoral dissertation]. East Tennessee State University; 1987. [cited 2019 Dec 06].
Available from: https://dc.etsu.edu/etd/2786.
Council of Science Editors:
Sanders TA. Quantitation of Teratogenic Effects of 5-fluorouracil Administered to Mice in Vivo or in Submerged Limb Culture. [Doctoral Dissertation]. East Tennessee State University; 1987. Available from: https://dc.etsu.edu/etd/2786

Stellenbosch University
9.
Mady-Goma, Chancy Rosine.
Clinical implications of the variations of sciatic nerve bifurcation on the popliteal nerve block.
Degree: MSc, Biomedical Sciences, 2018, Stellenbosch University
URL: http://hdl.handle.net/10019.1/104922
► ENGLISH ABSTRACT: The sciatic nerve (SN) is a major nerve of the lower limb, innervating the posterior thigh, the hip and knee as well as…
(more)
▼ ENGLISH ABSTRACT: The sciatic nerve (SN) is a major nerve of the lower limb, innervating the posterior thigh, the
hip and knee as well as structures below the knee through its branches. The SN division occurs
in the popliteal fossa (PF) at the level of the knee. However, various studies report great
variations in the level of division of the SN, ranging between 3.3 and 65.1%. These variations
were suggested as a possible cause in failures of the popliteal block (PB). Therefore, the aim
of this study is to describe the level of division of the SN in a South African cohort and to
evaluate the success rate of three approaches to the PB. Following the simulation of the PB in
22 lower limb specimens, the popliteal fossae of 61 cadavers were dissected and the sciatic
nerve properly exposed. The level of division was described and the location and distance between the dye and the nerve measured. Variations represented only 11.48% of cases, similar
to textbooks’ description (12%). The bifurcation pattern of the SN in this South African cohort
was therefore comparable to the standard one. The distance between the SN and the PC varied
between 20 mm and 405 mm, with a median of 55 mm, close to 60 – 70 mm found in most
studies. The prevalence of variations was higher in females (ratio F:M=2.78) and 55.56% were
bilateral. With the SN dividing in the PF, the simulation predicted a 100% success rate with no
difference between the approaches used. Nevertheless, a higher division of the SN would
compromise the success of the block. Overall, the SN division in our study population follows
the normal pattern with a lesser degree of variations (11.48%). The division of the nerve in the PF might ensure a successful block in 95 to 100% of cases, in contrast to cases of high
variations. Nevertheless, a preoperative imagery is strongly recommended, especially in women for early identification of variations to avoid failures of the PB, irrespective of the approach used.
AFRIKAANSE OPSOMMING: N. ischiadicus is 'n hoof senuwee in die onderste ledemaat, wat die posterior kompartement van die dy, en die heup en knie voorsien, asook strukture onder die knie deur takke afkomstig vanaf die senuwee. Verdeling van n. ischiadicus vind plaas in die popliteale fossa (PF) op die vlak van die knie. Verskeie studies toon egter ʼn groot aantal variasies, wat wissel tussen 3.3% en 65.1%, ten opsigte van die vlak van verdeling van die senuwee. Daar is voorgestel dat hierdie variasies moontlik die oorsaak van mislukte toediening van ʼn popliteale blok (PB) kan wees. Die doel van hierdie studie is dus om die vlak van verdeling van n. ischiadicus in 'n Suid-Afrikaanse kohort te beskryf, en die voorkoms van sukses ten opsigte van drie benaderings tot die toediening van ʼn PB te evalueer. Na simulasie toediening van ʼn PB in 22 onderste ledemaatmonsters, is die popliteale fossa in 61 kadawers oopgedissekteer en n. ischiadicus blootgelê. Die vlak van verdeling is beskryf, en die ligging van die kleurstof en afstand tussen die kleurstof en die…
Advisors/Committee Members: Tchokonte-Nana, Venant, Ben, Page, Stellenbosch University. Faculty of Health and Medical Sciences. Dept. of Biomedical Sciences. Anatomy and Histology..
Subjects/Keywords: Anatomy; Sciatic nerve; Sciatic nerve – Diseases; Popliteal fossa; UCTD
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APA ·
Chicago ·
MLA ·
Vancouver ·
CSE |
Export
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APA (6th Edition):
Mady-Goma, C. R. (2018). Clinical implications of the variations of sciatic nerve bifurcation on the popliteal nerve block. (Masters Thesis). Stellenbosch University. Retrieved from http://hdl.handle.net/10019.1/104922
Chicago Manual of Style (16th Edition):
Mady-Goma, Chancy Rosine. “Clinical implications of the variations of sciatic nerve bifurcation on the popliteal nerve block.” 2018. Masters Thesis, Stellenbosch University. Accessed December 06, 2019.
http://hdl.handle.net/10019.1/104922.
MLA Handbook (7th Edition):
Mady-Goma, Chancy Rosine. “Clinical implications of the variations of sciatic nerve bifurcation on the popliteal nerve block.” 2018. Web. 06 Dec 2019.
Vancouver:
Mady-Goma CR. Clinical implications of the variations of sciatic nerve bifurcation on the popliteal nerve block. [Internet] [Masters thesis]. Stellenbosch University; 2018. [cited 2019 Dec 06].
Available from: http://hdl.handle.net/10019.1/104922.
Council of Science Editors:
Mady-Goma CR. Clinical implications of the variations of sciatic nerve bifurcation on the popliteal nerve block. [Masters Thesis]. Stellenbosch University; 2018. Available from: http://hdl.handle.net/10019.1/104922

University of California – San Francisco
10.
Phan, Vernon T.
The Ras-GAP Proteins Ira2 and Neurofibromin Are Negatively Regulated by Ubiquitin-associated Proteins Gpb1 in Yeast and ETEA/UBXD8 in Human Cells.
Degree: Biomedical Sciences, 2008, University of California – San Francisco
URL: http://www.escholarship.org/uc/item/8st7h9w5
► The Neurofibromatosis type 1 (NF1) gene encodes the GTPase activating protein (GAP) neurofibromin which negatively regulates Ras activity. The yeast Saccharomyces cerevisiae has two neurofibromin…
(more)
▼ The Neurofibromatosis type 1 (NF1) gene encodes the GTPase activating protein (GAP) neurofibromin which negatively regulates Ras activity. The yeast Saccharomyces cerevisiae has two neurofibromin homologs, Ira1 and Ira2. Similar to mammalian cells, mutations or deletions of the IRA genes result in hyperactive Ras. I utilized an unbiased proteomics approach to investigate Ira2 and neurofibromin binding partners and their involvement in regulating Ras signaling. I demonstrated that the Gpb1 protein negatively regulates Ira2 by promoting Ira2 proteolysis. Loss and gain of function experiments showed the Gpb1 protein is essential for Ira2 function. Whereas deletion of GPB1 increased Ira2 protein levels, overexpression of Gpb1 destabilized Ira2. In addition, the purified Gpb1complex can ubiquitinate Ira2 in vitro. I demonstrated that Gpb1 is required for the Rpn1 proteasome base subunit to trigger Ira2 proteolysis. In addition, I showed that the deubiquitination enzyme Ubp6 interacts with Ira2 and antagonizes Gpb1-mediated degradation of Ira2. Finally, I showed that the serine/threonine kinase CK2 binds and phosphorylates Ira2, preventing Ira2 from protein degradation. I extended the findings to the mammalian system to show that the ETEA/UBXD8 protein directly interacts and negatively regulates neurofibromin. ETEA contains both UBA and UBX domains. Similar to Gpb1 negative regulation of Ira2 in yeast, ETEA over-expression down-regulates neurofibromin in human cells. Purified ETEA, but not a mutant of ETEA that lacks the UBX domain, ubiquitinates the neurofibromin GAP-related domain in vitro. Importantly, ETEA shares approximately 18% homology with Gpb1 N-terminal domain, including amino acid sequence homology in the UBA and UBX domains. Silencing of ETEA increases neurofibromin levels and downregulates Ras activities. These findings provide evidence for conserved ubiquitination pathways regulating the RasGAP proteins Ira2 in yeast and neurofibromin in humans.
Subjects/Keywords: Biology, Anatomy; Health Sciences, Oncology
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❌
APA ·
Chicago ·
MLA ·
Vancouver ·
CSE |
Export
to Zotero / EndNote / Reference
Manager
APA (6th Edition):
Phan, V. T. (2008). The Ras-GAP Proteins Ira2 and Neurofibromin Are Negatively Regulated by Ubiquitin-associated Proteins Gpb1 in Yeast and ETEA/UBXD8 in Human Cells. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/8st7h9w5
Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
Chicago Manual of Style (16th Edition):
Phan, Vernon T. “The Ras-GAP Proteins Ira2 and Neurofibromin Are Negatively Regulated by Ubiquitin-associated Proteins Gpb1 in Yeast and ETEA/UBXD8 in Human Cells.” 2008. Thesis, University of California – San Francisco. Accessed December 06, 2019.
http://www.escholarship.org/uc/item/8st7h9w5.
Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
MLA Handbook (7th Edition):
Phan, Vernon T. “The Ras-GAP Proteins Ira2 and Neurofibromin Are Negatively Regulated by Ubiquitin-associated Proteins Gpb1 in Yeast and ETEA/UBXD8 in Human Cells.” 2008. Web. 06 Dec 2019.
Vancouver:
Phan VT. The Ras-GAP Proteins Ira2 and Neurofibromin Are Negatively Regulated by Ubiquitin-associated Proteins Gpb1 in Yeast and ETEA/UBXD8 in Human Cells. [Internet] [Thesis]. University of California – San Francisco; 2008. [cited 2019 Dec 06].
Available from: http://www.escholarship.org/uc/item/8st7h9w5.
Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
Council of Science Editors:
Phan VT. The Ras-GAP Proteins Ira2 and Neurofibromin Are Negatively Regulated by Ubiquitin-associated Proteins Gpb1 in Yeast and ETEA/UBXD8 in Human Cells. [Thesis]. University of California – San Francisco; 2008. Available from: http://www.escholarship.org/uc/item/8st7h9w5
Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Stellenbosch University
11.
Dreyer, Rita Liezl.
Anatomical variation of the carotid bifurcation in a Stellenbosch University cadaver cohort.
Degree: MSc, Biomedical Sciences, 2019, Stellenbosch University
URL: http://hdl.handle.net/10019.1/105882
► ENGLISH ABSTRACT: The carotid bifurcation is the point where the common carotid artery bifurcates into the internal and external carotid artery. A precise anatomical knowledge…
(more)
▼ ENGLISH ABSTRACT: The carotid bifurcation is the point where the common carotid artery bifurcates into the internal and external carotid artery. A precise anatomical knowledge of the carotid bifurcation is required for various medical specialities. The
anatomy of the carotid bifurcation influences the risks, location and prognosis of related pathology. Furthermore, the
anatomy of the carotid bifurcation affects treatment as it determines which surgical techniques can be used in an area of high risk. The aim of the study was to determine the anatomical variations of the carotid bifurcation in a Stellenbosch cadaver cohort. One hundred and twenty-eight specimens were examined. This research focuses on the height, angle, general structure, and diameters of the carotid bifurcation, as well as the length and diameter of the carotid sinus. The internal anatomical variation of the carotid bifurcation was added as the study progressed. This study used the gonion as the landmark when measuring height. The Stellenbosch cadaver cohort had a high frequency of high bifurcation with the mean distance of 2.12 cm on the right and 2.06 cm on the left.
The angle of bifurcation was 18.53° on the right and 20.24° on the left and was smaller than previous reports in the literature, which ranged between 51-67°. Females had a higher bifurcation and larger angle of bifurcation than males. Sex affected the correlation between angle and height of the bifurcation. The general structure correlated with the standard description and was not influenced by other factors pertaining to the carotid bifurcation, sex or age. Kinks were found in the internal and external carotid artery. The diameters of the carotid bifurcation were larger on the left than on the right. The height of the bifurcation did not influence the probability of kinks in this study, contrary to the literature. The diameters of the internal, external and common carotid arteries in addition to the carotid sinus diameter were larger on the left side and in males. The external carotid had the weakest correlation with the other diameters, which was due to the external carotid artery’s embryological origin. The length of the carotid sinus was 1.74 cm on the right and 1.83 cm on the left. The diameters and the length of the carotid sinus was larger in the males. All external variation slightly increased with age over time as the elasticity of arteries decreased. A variation of the flow diverter was observed in 59% of the cadaver cohort. Supplementary flow diverters were a rare abnormality observed in the internal, external and common carotid arteries. The reason for the carotid bifurcation to present with supplementary flow diverters is still up for debate as this has not been observed in living patients; however, a pathological origin was suggested. Folds in the common carotid were observed. Internal anatomical variation was not affected by external variation or age; however, men had a higher probability of presenting with variation. The Stellenbosch cadaver cohort illustrated…
Advisors/Committee Members: Page, Benedict John, Stellenbosch University. Faculty of Medicine and Health Sciences. Dept. of Biomedical Sciences: Anatomy and Histology..
Subjects/Keywords: UCTD; Bifurcation theory; Carotid sinus; Carotid artery; Anatomy – Variation
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❌
APA ·
Chicago ·
MLA ·
Vancouver ·
CSE |
Export
to Zotero / EndNote / Reference
Manager
APA (6th Edition):
Dreyer, R. L. (2019). Anatomical variation of the carotid bifurcation in a Stellenbosch University cadaver cohort. (Masters Thesis). Stellenbosch University. Retrieved from http://hdl.handle.net/10019.1/105882
Chicago Manual of Style (16th Edition):
Dreyer, Rita Liezl. “Anatomical variation of the carotid bifurcation in a Stellenbosch University cadaver cohort.” 2019. Masters Thesis, Stellenbosch University. Accessed December 06, 2019.
http://hdl.handle.net/10019.1/105882.
MLA Handbook (7th Edition):
Dreyer, Rita Liezl. “Anatomical variation of the carotid bifurcation in a Stellenbosch University cadaver cohort.” 2019. Web. 06 Dec 2019.
Vancouver:
Dreyer RL. Anatomical variation of the carotid bifurcation in a Stellenbosch University cadaver cohort. [Internet] [Masters thesis]. Stellenbosch University; 2019. [cited 2019 Dec 06].
Available from: http://hdl.handle.net/10019.1/105882.
Council of Science Editors:
Dreyer RL. Anatomical variation of the carotid bifurcation in a Stellenbosch University cadaver cohort. [Masters Thesis]. Stellenbosch University; 2019. Available from: http://hdl.handle.net/10019.1/105882

Stellenbosch University
12.
Bergsteedt, Bryan Jason.
The sciatic nerve division in the gluteal region in a South African population: An anatomical study.
Degree: MSc, Biomedical Sciences, 2019, Stellenbosch University
URL: http://hdl.handle.net/10019.1/105909
► ENGLISH ABSTRACT: The sciatic nerve is repeatedly involved in the daily medical practices of anaesthesia, neurology, orthopaedics and rehabilitative medicine. The sciatic nerve, and its…
(more)
▼ ENGLISH ABSTRACT: The sciatic nerve is repeatedly involved in the daily medical practices of anaesthesia, neurology, orthopaedics and rehabilitative medicine. The sciatic nerve, and its branches, are some of the most frequently injured nerves within the human body. A possible reason for injury could be related to an inadequate knowledge of the anatomical variations of this nerve. Adequate understanding of the anatomical variability within the gluteal region is vital for appropriate diagnosis, potential treatment of gluteal pathology and pain and population-specific anomalies.
To the author’s best knowledge, no previous study has described the anatomical variations in relation to the piriformis and sciatic nerve bifurcation within the South African population. Therefore, the aim of the study is to report the prevalence of anatomical variations within the course of the sciatic nerve in relation to the piriformis muscle. Additionally, to report the prevalence of the variations in the level of the sciatic nerve bifurcation. Lastly, to analyse the typical sciatic nerve and piriformis morphomety. The results obtained will be a comparison between sides, sexes, and population groups.
For the purpose of this study, lower limbs (𝑁=340) from 170 South African cadavers were selected for dissection and morphological analysis. These specimens consisted of 191 males and 149 females, and comprised of three South African subpopulation groups, namely, White/Caucasian (𝑛=232), Mixed race (𝑛=78) and South African Black (𝑛=30). The variations were recorded, classified and described. Piriformis and sciatic nerve parameters were measured morphometrically using a digital sliding calliper, and statistically analysed.
Analysis of the relationship between piriformis and the sciatic nerve resulted in 43 (12.65%) specimens that presented variations in the morphology, while 297 (87.35%) specimens presented normal anatomical features. Variations of these structures occurred predominantly in the South African White/Caucasian population. The bifurcation of the sciatic nerve occurred mainly in the popliteal fossa proper (79.6%). The width of the sciatic nerve was significantly larger in the White/Caucasian group (𝑝<0.05), in comparison to the other two groups. The mean length of the sciatic nerve was significantly larger in the male specimens (𝑝<0.05) in comparison to the female specimens.
It was found that the sciatic nerve commonly entered the gluteal region as a single trunk, through the infra-piriform space, inferior to the piriformis muscle. However, variations in the
anatomy of the sciatic nerve are common, and are vital in assessing clinical risk, and avoiding debilitating injury or incorrect pain diagnoses. To maintain best possible clinical practices requires regularly updated clinical skills in relation to accurate and relevant new anatomical knowledge. It is for this reason that studies, such as this one, ensure that vital research contributions are available for best clinical practice. Clear uniform landmarks for morphometric analysis…
Advisors/Committee Members: Greyling, L. M., Stellenbosch University. Faculty of Medicine and Health Sciences. Dept. of Biomedical Sciences: Anatomy and Histology..
Subjects/Keywords: Sciatic nerve; Piriformis; Morphology; Gluteal region; Bifurcation theory; Anatomy; Variations; UCTD
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❌
APA ·
Chicago ·
MLA ·
Vancouver ·
CSE |
Export
to Zotero / EndNote / Reference
Manager
APA (6th Edition):
Bergsteedt, B. J. (2019). The sciatic nerve division in the gluteal region in a South African population: An anatomical study. (Masters Thesis). Stellenbosch University. Retrieved from http://hdl.handle.net/10019.1/105909
Chicago Manual of Style (16th Edition):
Bergsteedt, Bryan Jason. “The sciatic nerve division in the gluteal region in a South African population: An anatomical study.” 2019. Masters Thesis, Stellenbosch University. Accessed December 06, 2019.
http://hdl.handle.net/10019.1/105909.
MLA Handbook (7th Edition):
Bergsteedt, Bryan Jason. “The sciatic nerve division in the gluteal region in a South African population: An anatomical study.” 2019. Web. 06 Dec 2019.
Vancouver:
Bergsteedt BJ. The sciatic nerve division in the gluteal region in a South African population: An anatomical study. [Internet] [Masters thesis]. Stellenbosch University; 2019. [cited 2019 Dec 06].
Available from: http://hdl.handle.net/10019.1/105909.
Council of Science Editors:
Bergsteedt BJ. The sciatic nerve division in the gluteal region in a South African population: An anatomical study. [Masters Thesis]. Stellenbosch University; 2019. Available from: http://hdl.handle.net/10019.1/105909

Stellenbosch University
13.
Alblas, Amanda.
Assessment of health status in a 20th century skeletal collection from the Western Cape.
Degree: PhD, Biomedical Sciences, 2019, Stellenbosch University
URL: http://hdl.handle.net/10019.1/106020
► ENGLISH ABSTRACT: Studies on the health status of skeletal remains give insight into the standard of living and survival pattern of historic populations. Analysis of…
(more)
▼ ENGLISH ABSTRACT: Studies on the health status of skeletal remains give insight into the standard of living and survival pattern of historic populations. Analysis of trauma and pathological conditions in human skeletal remains are important in biological anthropology, explaining patterns of malnutrition, stress, disease and trauma in a population. However, the difficulty to overcome is the fact that the majority of skeletal pathological conditions are limited in their interpretive significance, since they are nonspecific and a range of stressors can cause the lesions. By analysing multiple conditions within a known population, pathological responses for specific insults can be outlined and in return help in interpretation of the frequencies and distributions within and between populations.
The Kirsten Skeletal Collection, housed at Stellenbosch University, Division of Clinical
Anatomy broadly represents individuals from mainly low socio-economic communities of different population groups in the Western Cape, dating throughout the 20th century. The aim of this study was to macroscopically and radiologically examine adult individuals (n=624, nmales=438, nfemales=186) in this collection for skeletal markings that included malnutrition (diet and metabolic deficiencies), osteoarthritic lesions, neoplasms, infective diseases and antemortem trauma lesions to be used as baseline information in further anthropological studies on the people of the Western Cape region. Statistically, the prevalence of specific diseases or trauma were correlated between the sexes, three different age-at-death and population groups as well as three different time periods throughout the 20th century using two-way frequency-tests and correspondence analyses.
During the 20th century, many factors resulted in poverty, and "non white” people, namely the South African Black (SAB) and South African Coloured (SAC) population groups, was especially disadvantaged by the laws introduced by the ruling political party. The influx of people from rural areas during World War II to work in the manufacturing industry resulted in the already overcrowded, unsanitary informal settlements around the Cape Peninsula to be flooded, influencing the disease patterns in the communities.
The results demonstrated that the lowest prevalence of metabolic deficiencies, iron deficiency anaemia (porotic hyperostosis), growth arrest signs (Harris’ lines), infections such as tuberculosis, osteomyelitis and non-specific periosteal reactions were observed in the South African White (SAW) population group. This confirms that higher socio economic societies, that escaped the unsanitary conditions associated with poor housing and overcrowding environments, were more succesfully buffering themselves from malnutrition and exposure to pathogens. Better dental health as well as dental fillings were also more associated with the SAW population group that had unrestrained access to dentists and health care facilities. In contrast, the ‘non-white’ population groups, that were supressed…
Advisors/Committee Members: Friedling, Louise Jacqui, Greyling, Linda Magdalena, Stellenbosch University. Faculty of Medicine and Health Science. Dept. of Biomedical Sciences: Anatomy and Histology..
Subjects/Keywords: Kirsten Skeletal Collection; Human skeleton – Abnormalities; Anatomy, Pathological
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❌
APA ·
Chicago ·
MLA ·
Vancouver ·
CSE |
Export
to Zotero / EndNote / Reference
Manager
APA (6th Edition):
Alblas, A. (2019). Assessment of health status in a 20th century skeletal collection from the Western Cape. (Doctoral Dissertation). Stellenbosch University. Retrieved from http://hdl.handle.net/10019.1/106020
Chicago Manual of Style (16th Edition):
Alblas, Amanda. “Assessment of health status in a 20th century skeletal collection from the Western Cape.” 2019. Doctoral Dissertation, Stellenbosch University. Accessed December 06, 2019.
http://hdl.handle.net/10019.1/106020.
MLA Handbook (7th Edition):
Alblas, Amanda. “Assessment of health status in a 20th century skeletal collection from the Western Cape.” 2019. Web. 06 Dec 2019.
Vancouver:
Alblas A. Assessment of health status in a 20th century skeletal collection from the Western Cape. [Internet] [Doctoral dissertation]. Stellenbosch University; 2019. [cited 2019 Dec 06].
Available from: http://hdl.handle.net/10019.1/106020.
Council of Science Editors:
Alblas A. Assessment of health status in a 20th century skeletal collection from the Western Cape. [Doctoral Dissertation]. Stellenbosch University; 2019. Available from: http://hdl.handle.net/10019.1/106020

East Tennessee State University
14.
Levee, Kathryn E.
Gross and Histological Features of a Myofascial Trigger Point in the Upper Trapezius.
Degree: PhD, Biomedical Sciences, 1996, East Tennessee State University
URL: https://dc.etsu.edu/etd/2938
► The purpose of this study was to precisely locate, in living humans, a myofascial trigger point associated with the upper portion of the trapezius…
(more)
▼ The purpose of this study was to precisely locate, in living humans, a myofascial trigger point associated with the upper portion of the trapezius muscle (TrP1) that refers pain to the head and neck and to determine if this point is associated with anatomical structures. This study is descriptive and utilizes data from measurements of the location of TrP1 in relation to anatomical landmarks, of pressure sensitivity overlying the trigger point and electromyography recordings in localizing the trigger point. Information obtained from living humans was used to determine anatomical correlation to structures in cadavers. Results indicated there is little variability in the location of TrP1 among individuals or from one extremity to the other, and this point may be associated with structures of the skin. A neurovascular supply (NAV) emerging from the upper trapezius to the skin was located in cadavers resembling the location of TrP1 in living humans. This NAV contained only small diameter nociceptive nerve fibers. Conclusion from the study show that TrP1 in living humans can be precisely located and that the mechanism of pain referral may involve structures of the skin. Future studies to precisely locate other myofascial trigger points may aid in identifying mechanisms of trigger point activation as well as aid clinicians in more precisely locating trigger points for treatment.
Subjects/Keywords: Anatomy and physiology; Biological sciences; Headache; Neurology; Pain; Anatomy; Neurology; Physiology
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APA ·
Chicago ·
MLA ·
Vancouver ·
CSE |
Export
to Zotero / EndNote / Reference
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APA (6th Edition):
Levee, K. E. (1996). Gross and Histological Features of a Myofascial Trigger Point in the Upper Trapezius. (Doctoral Dissertation). East Tennessee State University. Retrieved from https://dc.etsu.edu/etd/2938
Chicago Manual of Style (16th Edition):
Levee, Kathryn E. “Gross and Histological Features of a Myofascial Trigger Point in the Upper Trapezius.” 1996. Doctoral Dissertation, East Tennessee State University. Accessed December 06, 2019.
https://dc.etsu.edu/etd/2938.
MLA Handbook (7th Edition):
Levee, Kathryn E. “Gross and Histological Features of a Myofascial Trigger Point in the Upper Trapezius.” 1996. Web. 06 Dec 2019.
Vancouver:
Levee KE. Gross and Histological Features of a Myofascial Trigger Point in the Upper Trapezius. [Internet] [Doctoral dissertation]. East Tennessee State University; 1996. [cited 2019 Dec 06].
Available from: https://dc.etsu.edu/etd/2938.
Council of Science Editors:
Levee KE. Gross and Histological Features of a Myofascial Trigger Point in the Upper Trapezius. [Doctoral Dissertation]. East Tennessee State University; 1996. Available from: https://dc.etsu.edu/etd/2938

Stellenbosch University
15.
Nel, Simoné.
Histomorphometric effects of an antiretroviral treatment and obesity on the pancreas, liver, kidney and perivascular adipose tissue in a rat model.
Degree: MSc, Biomedical Sciences, 2017, Stellenbosch University
URL: http://hdl.handle.net/10019.1/102974
► ENGLISH ABSTRACT : Human immunodeficiency virus (HIV)-infected patients receiving antiretroviral treatment (ART) may develop metabolic syndrome and lipodystrophy, leading to obesity rather than wasting. Obesity…
(more)
▼ ENGLISH ABSTRACT : Human immunodeficiency virus (HIV)-infected patients receiving antiretroviral treatment (ART) may develop metabolic syndrome and lipodystrophy, leading to obesity rather than wasting. Obesity is associated with metabolic homeostasis disruptions leading to pancreatic toxicity, diabetes, renal vasodilation and compression as well as liver steatosis. In addition, patients on long-term combination antiretroviral treatment (cART) can develop pancreatitis, nephrotoxicity, hepatic steatosis, and diabetes. This study aims to investigate the effects of cART combined with a high-calorie diet (HCD) on the histomorphometry of the pancreas, kidney, liver, and aortic perivascular adipose tissue (PVAT) leptin expression in the rat. Male Wistar rats (N=40) were divided into four groups (n=10); C/ART- (lean control), C/ART+ (ART control), HCD/ART- (HCD control) and HCD/ART+ (HCD and ART). The aorta with surrounding PVAT, pancreas, liver and kidney were harvested and processed to wax. Pancreas sections underwent a double immunohistochemistry (IHC) labelling for insulin and glucagon and reactive cell areas were measured. Aortic PVAT was labelled with anti-leptin and the staining intensity classified accordingly. Kidney sections underwent haematoxylin and eosin (H&E) stain measuring the areas of the renal corpuscles, glomeruli, renal spaces as well as the renal arcuate arteries lumen diameter and artery wall thickness. Pancreatic, kidney and liver sections underwent H&E staining which were used for pathology assessment.
The HCD/ART+ had a significant body mass increase compared to the C/ART-, suggesting ART combined with a HCD causes body mass increase. Unilocular and differentiating adipocytes in the C/ART+ had intense leptin staining, suggesting ART may lead to increased leptin expression in aortic PVAT. Unilocular and differentiating adipocytes in the HCD/ART- and HCD/ART+ had weak to no leptin intensity, suggesting possible leptin deficiency with a HCD. The C/ART+ showed a trend in smaller total pancreatic islet area compared to the C/ART-, suggesting that islets underwent possible hypotrophy with ART. Based on the average values, alpha-cells were increased in the HCD/ART-, whereas beta-cells decreased in the ART and HCD. This suggests that a HCD potentially increases glucagon secreting area, whereas ART and a HCD leads to β-cell mass loss. The HCD/ART- and HCD/ART+ showed a trend in increased number of islets per section compared to the C/ART-, suggesting that HCD leads to new forming islets. Based on the average values, the renal corpuscle, glomeruli and renal space sizes were increased in the HCD/ART- compared to the other groups, although not significantly. A trend in the HCD/ART+ showed increased arcuate artery lumen diameter and tunica media thickness, whereas the C/ART+ had increased tunica adventitia compared to the C/ART-. This suggests that ART combined with a HCD causes hypertrophic remodelling in the tunica media and hypotrophic remodelling in the tunica adventitia. All groups had mild vacuolisation…
Advisors/Committee Members: Kotzé, Sanet Henriette, Nireshni, Chellan, Stellenbosch University. Faculty of Medicine and Health Sciences. Dept. of Biomedical Sciences. Division Anatomy and Histology..
Subjects/Keywords: Immunohistochemistry; UCTD; Rats – Antiretroviral treatment; Rats as laboratory animals; Obesity – Animal models; Organs (Anatomy) – Side effects
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APA (6th Edition):
Nel, S. (2017). Histomorphometric effects of an antiretroviral treatment and obesity on the pancreas, liver, kidney and perivascular adipose tissue in a rat model. (Masters Thesis). Stellenbosch University. Retrieved from http://hdl.handle.net/10019.1/102974
Chicago Manual of Style (16th Edition):
Nel, Simoné. “Histomorphometric effects of an antiretroviral treatment and obesity on the pancreas, liver, kidney and perivascular adipose tissue in a rat model.” 2017. Masters Thesis, Stellenbosch University. Accessed December 06, 2019.
http://hdl.handle.net/10019.1/102974.
MLA Handbook (7th Edition):
Nel, Simoné. “Histomorphometric effects of an antiretroviral treatment and obesity on the pancreas, liver, kidney and perivascular adipose tissue in a rat model.” 2017. Web. 06 Dec 2019.
Vancouver:
Nel S. Histomorphometric effects of an antiretroviral treatment and obesity on the pancreas, liver, kidney and perivascular adipose tissue in a rat model. [Internet] [Masters thesis]. Stellenbosch University; 2017. [cited 2019 Dec 06].
Available from: http://hdl.handle.net/10019.1/102974.
Council of Science Editors:
Nel S. Histomorphometric effects of an antiretroviral treatment and obesity on the pancreas, liver, kidney and perivascular adipose tissue in a rat model. [Masters Thesis]. Stellenbosch University; 2017. Available from: http://hdl.handle.net/10019.1/102974

Stellenbosch University
16.
Witbooi, Lee-Roy Cecil.
Accurate estimation of large vessel length in growing children and adolescents for the purpose of pulse wave velocity calculation.
Degree: MMed, Biomedical Sciences, 2018, Stellenbosch University
URL: http://hdl.handle.net/10019.1/105087
► Background Cardiovascular disease is a major cause of death in adults worldwide. Early detection allows for early intervention to prevent vascular events such as strokes,…
(more)
▼ Background
Cardiovascular disease is a major cause of death in adults worldwide. Early detection allows for
early intervention to prevent vascular events such as strokes, heart attacks, etc. Although these
vascular events typically occur in late adulthood, the underlying atherosclerosis often begins
during childhood. Early subclinical atherosclerosis can be detected by measuring the elasticity of
the large arteries, particularly when performed serially over time. Normally, the elasticity of a
healthy aorta helps to slow down the speed of the pressure wave created by contraction of the
heart muscle. This is an important way of maintaining smooth laminar blood flow.
Atherosclerosis causes the vessel wall to harden and lose elasticity. As the vessel wall hardens,
the speed of the pressure wave increases.
Pulse wave velocity (PWV) is a sophisticated method of detecting early elasticity changes, and is
a preferred non-invasive technique to measure arterial wall stiffness. The velocity calculation
requires accurate measurement of both distance travelled and time taken for the pulse wave to
travel between two points. The distance used for pulse wave velocity calculation is an
approximation of the intraluminal distance travelled by the pulse wave and is estimated by
measuring the distance between various surface
anatomy landmarks. The expert consensus
document on arterial wall stiffness described carotid–femoral PWV as the “gold standard”
measurement of arterial wall stiffness, yet there is no consensus on the arterial path length
estimation method. A variety of arterial path length estimation methods exist, and this makes
inter-study comparison of PWV very difficult.
The purpose of the current study was to investigate the most accurate method of estimating the
true distance travelled by the aorto-femoral pressure wave. We compared distances between a
range of commonly used surface
anatomy landmarks, and compared these to the true
intraluminal distance measured on multi-planar reformations of archived computerized
tomography imaging in children of varying ages. Our findings will allow standardization of
PWV calculation in children and allow for inter-study comparisons.
Methods
Vessel lengths in children (aged 0-18 years) were measured with multi-planar reformation (MPR) imaging software. These measurements were then compared with the surface
anatomy measurements also obtained using the MPR imaging software. The comparisons between vessel lengths and surface
anatomy distances were performed in segments, since there were no whole body CT scans available on the Picture Archiving and Communication System (PACS) at the research site.
Results
The surface
anatomy measurements from the suprasternal notch to the angle of the mandible (on the right) correlated well with the intraluminal vessel length from the origin of the brachiocephalic trunk to the external carotid at the angle of the mandible (r2=0.92; p<0.0001). The surface
anatomy measurements from the suprasternal notch to the midpoint of the right…
Advisors/Committee Members: Innes, Steve, Page, Ben, Pitcher, Richard, Stellenbosch University. Faculty of Medicine and Health Sciences. Dept. of Biomedical Sciences. Anatomy and Histology..
Subjects/Keywords: Vascular diseases; Cardiovascular diseases; Atherosclerosis; Children; Adolescents; Surface anatomy; Pulse wave velocity; Multidetector-row helical computed tomography; Body section radiography; UCTD
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❌
APA ·
Chicago ·
MLA ·
Vancouver ·
CSE |
Export
to Zotero / EndNote / Reference
Manager
APA (6th Edition):
Witbooi, L. C. (2018). Accurate estimation of large vessel length in growing children and adolescents for the purpose of pulse wave velocity calculation. (Thesis). Stellenbosch University. Retrieved from http://hdl.handle.net/10019.1/105087
Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
Chicago Manual of Style (16th Edition):
Witbooi, Lee-Roy Cecil. “Accurate estimation of large vessel length in growing children and adolescents for the purpose of pulse wave velocity calculation.” 2018. Thesis, Stellenbosch University. Accessed December 06, 2019.
http://hdl.handle.net/10019.1/105087.
Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
MLA Handbook (7th Edition):
Witbooi, Lee-Roy Cecil. “Accurate estimation of large vessel length in growing children and adolescents for the purpose of pulse wave velocity calculation.” 2018. Web. 06 Dec 2019.
Vancouver:
Witbooi LC. Accurate estimation of large vessel length in growing children and adolescents for the purpose of pulse wave velocity calculation. [Internet] [Thesis]. Stellenbosch University; 2018. [cited 2019 Dec 06].
Available from: http://hdl.handle.net/10019.1/105087.
Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
Council of Science Editors:
Witbooi LC. Accurate estimation of large vessel length in growing children and adolescents for the purpose of pulse wave velocity calculation. [Thesis]. Stellenbosch University; 2018. Available from: http://hdl.handle.net/10019.1/105087
Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
17.
Lafferty, Dennis Craig.
The mGluR2/3 Agonist LY397268 Improves Morphometric and Behavioral Outcomes in R6/2 Huntington's Disease Mice.
Degree: MS, Biomedical Sciences, 2010, University of Tennessee Health Science Center
URL: https://dc.uthsc.edu/dissertations/152
► A prominent theory for the pathology of Huntington's Disease (HD) is the excitotoxic injury to the striatum. Continual exposure of ionotropic NMDA receptors to…
(more)
▼ A prominent theory for the pathology of Huntington's Disease (HD) is the excitotoxic injury to the striatum. Continual exposure of ionotropic NMDA receptors to glutamate from the cortex can be excitotoxic in HD and leave striatal neurons vulnerable to damage. Activation of presynaptic mGluR2/3 by an agonist dampens glutamate release from corticostriatal terminals. Treatments that target excitoxicity and oxidative stress thus may improve some of the symptoms in HD patients and it is therefore logical to pursue therapies aimed in this direction. LY379268 is an inviting mGluR2/3 agonist that has been shown to be neuroprotective in hypoxic and ischemic injuries to cultured neurons. Daily subcutaneous injection of 20mg/kg LY379268 had a number of beneficial effects in R6/2 mice, including an 11% improvement in lifespan and various locomotor parameters. The drug showed improvement in open field measurements of overall activity, speed, acceleration, and endurance. Histological and tissue analysis revealed a reduced lateral ventricle enlargement when compared to vehicle-treated R6/2 mice. There was a 20% loss of cortical and striatal neurons in R6/2 mice, which was rescued with the administration of LY379268. There was no effect of the drug on neuronal intranuclear inclusions (NIIs) or ENK+ striatal neurons, but SP+ striatal projection neurons were normalized in their neurochemistry. The R6/2 data indicate that LY379268 is particularly useful in improving the health and functioning of the direct striatal pathway (i.e. SP+ neurons), which demonstrably improved the voluntary motor behavior in the R6/2 mice.
Advisors/Committee Members: Anton Reiner, Ph.D..
Subjects/Keywords: Basal Ganglia; Huntington’s Disease; Diseases; Medical Anatomy; Medical Sciences; Medicine and Health Sciences; Nervous System Diseases; Neurosciences
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APA ·
Chicago ·
MLA ·
Vancouver ·
CSE |
Export
to Zotero / EndNote / Reference
Manager
APA (6th Edition):
Lafferty, D. C. (2010). The mGluR2/3 Agonist LY397268 Improves Morphometric and Behavioral Outcomes in R6/2 Huntington's Disease Mice. (Thesis). University of Tennessee Health Science Center. Retrieved from https://dc.uthsc.edu/dissertations/152
Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
Chicago Manual of Style (16th Edition):
Lafferty, Dennis Craig. “The mGluR2/3 Agonist LY397268 Improves Morphometric and Behavioral Outcomes in R6/2 Huntington's Disease Mice.” 2010. Thesis, University of Tennessee Health Science Center. Accessed December 06, 2019.
https://dc.uthsc.edu/dissertations/152.
Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
MLA Handbook (7th Edition):
Lafferty, Dennis Craig. “The mGluR2/3 Agonist LY397268 Improves Morphometric and Behavioral Outcomes in R6/2 Huntington's Disease Mice.” 2010. Web. 06 Dec 2019.
Vancouver:
Lafferty DC. The mGluR2/3 Agonist LY397268 Improves Morphometric and Behavioral Outcomes in R6/2 Huntington's Disease Mice. [Internet] [Thesis]. University of Tennessee Health Science Center; 2010. [cited 2019 Dec 06].
Available from: https://dc.uthsc.edu/dissertations/152.
Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
Council of Science Editors:
Lafferty DC. The mGluR2/3 Agonist LY397268 Improves Morphometric and Behavioral Outcomes in R6/2 Huntington's Disease Mice. [Thesis]. University of Tennessee Health Science Center; 2010. Available from: https://dc.uthsc.edu/dissertations/152
Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
18.
Narayanan, Damodaran.
Mitochondrial Regulation of Arterial Contractility.
Degree: PhD, Biomedical Sciences, 2010, University of Tennessee Health Science Center
URL: https://dc.uthsc.edu/dissertations/177
► Rationale: Physiological functions of mitochondria in contractile arterial smooth muscle cells are poorly understood. Mitochondria can uptake calcium (Ca2+), but intracellular Ca2+ signals that…
(more)
▼ Rationale: Physiological functions of mitochondria in contractile arterial smooth muscle cells are poorly understood. Mitochondria can uptake calcium (Ca
2+), but intracellular Ca
2+ signals that regulate mitochondrial Ca
2+ concentration ([Ca
2+]
mito) and physiological functions of changes in [Ca
2+]
mito in arterial smooth muscle cells are unclear.
Objective: Identify Ca
2+ signals that regulate [Ca
2+]
mito, examine the significance of changes in [Ca
2+]
mito, and test the hypothesis that [Ca
2+]
mito controls functional ion channel transcription in smooth muscle cells of resistance–size cerebral arteries.
Methods and Results: Endothelin–1 (ET–1) activated Ca
2+ waves and elevated global Ca
2+ concentration ([Ca
2+]
i) via inositol 1,4,5–triphosphate receptor (IP
3R) activation. IP
3R–mediated sarcoplasmic reticulum (SR) Ca
2+ release increased [Ca
2+]
mito and induced mitochondrial depolarization, which stimulated mitochondrial reactive oxygen species (mitoROS) generation that elevated cytosolic ROS. In contrast, a global [Ca
2+]
i elevation did not alter [Ca
2+]
mito, mitochondrial potential, or mitoROS generation. ET–1 stimulated nuclear translocation of nuclear factor kappa B (NF–κB) p50 subunit and ET–1–induced IP
3R–mediated mitoROS elevated NF–κB–dependent transcriptional activity. ET–1 elevated voltage–dependent Ca
2+ (Ca
V1.2) channel expression, leading to an increase in both pressure (myogenic tone)– and depolarization–induced vasoconstriction. Baseline Ca
V1.2 expression and the ET–1–induced elevation in Ca
V1.2 expression were both reduced by IP
3R inhibition, mitochondrial electron transport chain block, antioxidant treatment, and NF–κB subunit knockdown, leading to vasodilation.
Conclusions: IP
3R–mediated SR Ca
2+ release elevates [Ca
2+]
mito, which induces mitoROS generation. MitoROS activate NF–κB, which stimulates Ca
V1.2 channel transcription. Thus, mitochondria sense IP
3R–mediated SR Ca
2+ release to control NF–κB–dependent Ca
V1.2 channel expression in arterial smooth muscle cells, thereby modulating arterial contractility.
Advisors/Committee Members: Jonathan H. Jaggar, Ph.D..
Subjects/Keywords: arterial smooth muscle; calcium signaling; CaV1.2 expression; mitochondria; myogenic tone; Anatomy; Cardiovascular System; Medicine and Health Sciences
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APA ·
Chicago ·
MLA ·
Vancouver ·
CSE |
Export
to Zotero / EndNote / Reference
Manager
APA (6th Edition):
Narayanan, D. (2010). Mitochondrial Regulation of Arterial Contractility. (Doctoral Dissertation). University of Tennessee Health Science Center. Retrieved from https://dc.uthsc.edu/dissertations/177
Chicago Manual of Style (16th Edition):
Narayanan, Damodaran. “Mitochondrial Regulation of Arterial Contractility.” 2010. Doctoral Dissertation, University of Tennessee Health Science Center. Accessed December 06, 2019.
https://dc.uthsc.edu/dissertations/177.
MLA Handbook (7th Edition):
Narayanan, Damodaran. “Mitochondrial Regulation of Arterial Contractility.” 2010. Web. 06 Dec 2019.
Vancouver:
Narayanan D. Mitochondrial Regulation of Arterial Contractility. [Internet] [Doctoral dissertation]. University of Tennessee Health Science Center; 2010. [cited 2019 Dec 06].
Available from: https://dc.uthsc.edu/dissertations/177.
Council of Science Editors:
Narayanan D. Mitochondrial Regulation of Arterial Contractility. [Doctoral Dissertation]. University of Tennessee Health Science Center; 2010. Available from: https://dc.uthsc.edu/dissertations/177

East Tennessee State University
19.
Abraham, Sonny T.
Denervation Supersensitivity of the Rat Vas Deferens: A Role for Protein Kinase C.
Degree: PhD, Biomedical Sciences, 1994, East Tennessee State University
URL: https://dc.etsu.edu/etd/2622
► A role for protein kinase C (PKC) in the denervation-induced supersensitivity of the rat vas deferens was investigated. Chronic, surgical denervation of the rat…
(more)
▼ A role for protein kinase C (PKC) in the denervation-induced supersensitivity of the rat vas deferens was investigated. Chronic, surgical denervation of the rat vas deferens (up to 8 days) resulted in tissues that produced enhanced contractile responses to norepinephrine (NE) in isolated organ baths. Single challenges of NE (10 μM) produced 0.6 ± 0.1 g of maximal tension in the control vas whereas in the paired, denervated tissue 2.2 ± 0.3 g of tension was recorded (n = 6). Cumulative concentration-effect curves to NE produced in the denervated vas deferens were shifted 18-fold to the left of the control response. Neurokinin A (NKA) responses after denervation of the tissue were not significantly different from the control. Denervation did not alter the contractile response to phorbol diacetate (PDA), a PKC activator. Pretreatment of denervated and control vas deferens with 100 μM nifedipine (a calcium channel blocker), significantly attenuated the contractile response to NE. The responses in the control tissues were depressed by 88%, those in the denervated vasa were only antagonized by 65% after nifedipine treatment. Exposure of denervated and control vas deferens to 100 μM NE resulted in no significant accumulation of diacylglycerol (DAG) from basal values. The molecular species of DAG produced after receptor stimulation, in either tissue group, were not different from those found in resting tissues. Denervation also had no effect on the binding characteristics of membrane-associated PKC when assayed using the specific ligand, (3H) phorbol dibutyrate. The PKC activity of resting vas deferens was not altered by chronic surgical denervation. Denervated and control vas deferens that were stimulated with 100 μM NE showed a time-dependent translocation of PKC from the cytosolic to the membrane fraction of the tissue. In both tissue groups exposure to NE resulted in a 3-4 fold increase in the membrane-bound PKC activity, which remained elevated above basal values for up to 20 min. The rate of translocation of PKC was faster in denervated vasa (maximal at 5 min after NE) when compared to the control (maximal at 20 min), but the maximal amount of the enzyme activated was the same for the two tissue groups. The ability of NKA, 60 mM K+-depolarization and PDB (PKC activator) to produce translocation of the PKC was not altered by denervation of the vas deferens. (Abstract shortened by UMI.)
Subjects/Keywords: Anatomy and physiology; Animals; Biological sciences; Health and environmental sciences; Pharmacology; Anatomy; Animal Structures; Pharmacology
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❌
APA ·
Chicago ·
MLA ·
Vancouver ·
CSE |
Export
to Zotero / EndNote / Reference
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APA (6th Edition):
Abraham, S. T. (1994). Denervation Supersensitivity of the Rat Vas Deferens: A Role for Protein Kinase C. (Doctoral Dissertation). East Tennessee State University. Retrieved from https://dc.etsu.edu/etd/2622
Chicago Manual of Style (16th Edition):
Abraham, Sonny T. “Denervation Supersensitivity of the Rat Vas Deferens: A Role for Protein Kinase C.” 1994. Doctoral Dissertation, East Tennessee State University. Accessed December 06, 2019.
https://dc.etsu.edu/etd/2622.
MLA Handbook (7th Edition):
Abraham, Sonny T. “Denervation Supersensitivity of the Rat Vas Deferens: A Role for Protein Kinase C.” 1994. Web. 06 Dec 2019.
Vancouver:
Abraham ST. Denervation Supersensitivity of the Rat Vas Deferens: A Role for Protein Kinase C. [Internet] [Doctoral dissertation]. East Tennessee State University; 1994. [cited 2019 Dec 06].
Available from: https://dc.etsu.edu/etd/2622.
Council of Science Editors:
Abraham ST. Denervation Supersensitivity of the Rat Vas Deferens: A Role for Protein Kinase C. [Doctoral Dissertation]. East Tennessee State University; 1994. Available from: https://dc.etsu.edu/etd/2622

East Tennessee State University
20.
Khalbuss, Walid E.
Electrophysiology, Cell Calcium, and Mechanisms of Hepatocyte Volume Regulation.
Degree: PhD, Biomedical Sciences, 1990, East Tennessee State University
URL: https://dc.etsu.edu/etd/2709
► The electrophysiologic technique (Reuss, L., Proc. Natl. Acad. Sci. USA 82:6014, 1985) was modified to measure changes in steady-state hepatocyte volume during osmotic stress.…
(more)
▼ The electrophysiologic technique (Reuss, L., Proc. Natl. Acad. Sci. USA 82:6014, 1985) was modified to measure changes in steady-state hepatocyte volume during osmotic stress. Hepatocytes in mouse liver slices were loaded with tetramethylammonium ion (TMA+) during transient exposure of cells to nystatin. Intracellular TMA+ activity (a i TMA) was measured with TMA+-sensitive, double-barreled microelectrodes. Loading hepatocytes with TMA+ did not change their membrane potential (V m), and under steady-state conditions a i TMA remained constant over 4 min in single impalements. Hyperosmotic solutions (50, 100, & 150 mM sucrose added to media) and hyposmotic solutions (sucrose in media reduced by 50 & 100 mM) increased and decreased a i TMA, respectively, which suggested transmembrane water movements. The regression coefficient of the ratio of control a i TMA/experimental a i TMA versus the relative osmolality of media (experimental mOsm/control mOsm) was -0.34 ± 0.03, p < 0.001, which is less than expected for a perfect osmometer. Corresponding measurements of V m showed that its magnitude increased with hyposmolality and decreased with hyperosmolality. When Ba2+ (2 mM) was present during hyposmotic stress of 0.66 × 286 mOsm (control), cell water volume increased by a factor of 1.44 ± 0.02 compared with that of hyposmotic stress alone, which increased cell water volume by a factor of only 1.12 ± 0.02, p < 0.001. Ba2+ also decreased the hyperpolarization of V m due to hyposmotic stress from a factor of 1.62 ± 0.04 to 1.24 ± 0.09, p < 0.01. When verapamil (50 μM) was present during hyposmotic stress of 0.69 × 292 mOsm (control), cell water volume increased by a factor of 1.42 ± 0.02 compared with that of hyposmotic stress alone, which increased cell water volume by a factor of only 1.19 ± 0.02, p < 0.001. Verapamil also decreased the hyperpolarization of V m due to hyposmotic stress from a factor of 1.34 ± 0.07 to 1.08 ± 0.08, p < 0.05. Similar results were obtained when exposing hepatocytes to Ca2+-free medium plus EGTA (5 mM). It was concluded that hepatocytes partially regulate their steady-state volume during hypo- and hyperosmotic stress. However, volume regulation during hyposmotic stress diminished along with hyperpolarization of V m in the presence of the K+-channel blocker, Ba2+, the Ca2+-channel blocker, verapamil and the Ca2+-chelator, EGTA. This indicated that cell calcium and membrane potassium conductance (g K) were involved in hepatocyte volume regulation mechanism and that variation in V m provides an intercurrent, electromotive force for hepatocyte volume regulation.
Subjects/Keywords: Anatomy and physiology; Animals; Biological sciences; Biology; Calcium; Cellular biology; Anatomy; Animal Structures; Biology; Cell Biology
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❌
APA ·
Chicago ·
MLA ·
Vancouver ·
CSE |
Export
to Zotero / EndNote / Reference
Manager
APA (6th Edition):
Khalbuss, W. E. (1990). Electrophysiology, Cell Calcium, and Mechanisms of Hepatocyte Volume Regulation. (Doctoral Dissertation). East Tennessee State University. Retrieved from https://dc.etsu.edu/etd/2709
Chicago Manual of Style (16th Edition):
Khalbuss, Walid E. “Electrophysiology, Cell Calcium, and Mechanisms of Hepatocyte Volume Regulation.” 1990. Doctoral Dissertation, East Tennessee State University. Accessed December 06, 2019.
https://dc.etsu.edu/etd/2709.
MLA Handbook (7th Edition):
Khalbuss, Walid E. “Electrophysiology, Cell Calcium, and Mechanisms of Hepatocyte Volume Regulation.” 1990. Web. 06 Dec 2019.
Vancouver:
Khalbuss WE. Electrophysiology, Cell Calcium, and Mechanisms of Hepatocyte Volume Regulation. [Internet] [Doctoral dissertation]. East Tennessee State University; 1990. [cited 2019 Dec 06].
Available from: https://dc.etsu.edu/etd/2709.
Council of Science Editors:
Khalbuss WE. Electrophysiology, Cell Calcium, and Mechanisms of Hepatocyte Volume Regulation. [Doctoral Dissertation]. East Tennessee State University; 1990. Available from: https://dc.etsu.edu/etd/2709

East Tennessee State University
21.
Miao, Kai.
Microcirculation: Electrophysiological Basis for the Response of Endothelial Cells to Inflammatory Mediators-bradykinin.
Degree: PhD, Biomedical Sciences, 1994, East Tennessee State University
URL: https://dc.etsu.edu/etd/2749
► Using conventional microelectrodes, I studied the electrical basis for determining the resting V m in intact EC's from hamsters. The resting V m were…
(more)
▼ Using conventional microelectrodes, I studied the electrical basis for determining the resting V m in intact EC's from hamsters. The resting V m were found to be -40 mV for aortic EC's and -43 mV for vena caval EC's. The contributions of ions to the resting V m of aortic EC's were compared in terms of the transference number (t ion). To develop a technique for in situ monitoring changes in V m of postcapillary venular EC's in the hamster mesentery, a voltage-sensitive fluorescent probe, bisoxonol, was used to load the cells and the fluorescence signals were analyzed under an intravital microscope by recording the fluorescence intensity (I f) and processing fluorescent images of the bisoxonol-loaded cells. Calibrations were conducted by simultaneously measuring changes in V m with microelectrodes and bisoxonol from aortic EC's and by varying extracellular Na+ in microvessels. Both calibrations yielded the linear relationship between V m and bisoxonol I f, showing the slope of 5.7%/mV for aortic EC's and 5.2%/mV for microvascular EC's. Altering extracellular K+ to 25, 50, and 100 mM in the suffusate depolarized microvascular EC's by 5, 8, and 10 mV; whereas, the same alterations via both suffusion and perfusion induced the depolarization by 18, 30, and 42 mV, indicating that the K+ conductance has an asymmetric distribution. Ba2+ (1 mM) produced a depolarization by 70 mV, suggesting that the activity of K+ channels dominates the resting V m. To correlate the bradykinin-induced increase in microvascular permeability to the changes in V m, the albumin flux (J A) was measured using TRITC-albumin along with monitoring V m. Bradykinin(l μM) induced a hyperpolarization of EC's by 8 mV and a biphasic increase in J A from the basal level of 1.00 x 10-6 to a transient peak of 9.17 x 10-6 followed by a sustained level of 3.05 x 10-6 cm/s. The linear correlations of net increases in both the peak and the sustained values of J A to changes in V m indicate that the hyperpolarization determines the peak in part and the sustained level in all. Under high K+ (50 mM), bradykinin produced a repolarization from a depolarized V m of -54 mV to -66 mV and a smaller increase in J A from the basal level of 0.38 x 10-6 to the peak of 5.51 x 10-6 followed by a significantly lowered, sustained level of 1.11 x 10-6 cm/s. The repolarization under high K+ indicates that besides the activation of Ca2+-dependent K+ channels, other electrical events may be implicated. The correlation between the repolarization and the lowered value of J A at the peak implies that this variation in V m also mediates the bradykinin-induced increase in J A under high K+ condition. (Abstract shortened by UMI.)
Subjects/Keywords: Anatomy and physiology; Animals; Biological sciences; Bradykinin; Cellular biology; Anatomy; Animal Structures; Cell Biology
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APA (6th Edition):
Miao, K. (1994). Microcirculation: Electrophysiological Basis for the Response of Endothelial Cells to Inflammatory Mediators-bradykinin. (Doctoral Dissertation). East Tennessee State University. Retrieved from https://dc.etsu.edu/etd/2749
Chicago Manual of Style (16th Edition):
Miao, Kai. “Microcirculation: Electrophysiological Basis for the Response of Endothelial Cells to Inflammatory Mediators-bradykinin.” 1994. Doctoral Dissertation, East Tennessee State University. Accessed December 06, 2019.
https://dc.etsu.edu/etd/2749.
MLA Handbook (7th Edition):
Miao, Kai. “Microcirculation: Electrophysiological Basis for the Response of Endothelial Cells to Inflammatory Mediators-bradykinin.” 1994. Web. 06 Dec 2019.
Vancouver:
Miao K. Microcirculation: Electrophysiological Basis for the Response of Endothelial Cells to Inflammatory Mediators-bradykinin. [Internet] [Doctoral dissertation]. East Tennessee State University; 1994. [cited 2019 Dec 06].
Available from: https://dc.etsu.edu/etd/2749.
Council of Science Editors:
Miao K. Microcirculation: Electrophysiological Basis for the Response of Endothelial Cells to Inflammatory Mediators-bradykinin. [Doctoral Dissertation]. East Tennessee State University; 1994. Available from: https://dc.etsu.edu/etd/2749

East Tennessee State University
22.
Tang, Tao.
Differential Role of the Endothelium in Regulating Microvascular Blood Flow.
Degree: PhD, Biomedical Sciences, 1994, East Tennessee State University
URL: https://dc.etsu.edu/etd/2802
► The vascular endothelial cell (EC) plays an important role in regulating vascular tone and local blood flow by sensing chemical and mechanical stimuli on…
(more)
▼ The vascular endothelial cell (EC) plays an important role in regulating vascular tone and local blood flow by sensing chemical and mechanical stimuli on the vascular wall and releasing a host of vasoactive substances upon activations of endogenous or exogenous vasoactive substances. The central hypothesis is that local control of blood now and autoregulatory behavior in the microcirculation is distinctive at different levels of the vasculature and is dependent on the cellular activities of the EC and its interaction with the local environment. The in vivo as well as the ex vivo, flow-controlled preparations of the hamster cheek pouch were utilized. Inhibition of Endothelium-Derive Relaxing Factor (EDRF) synthesis and the functional impairment by light-dye (L-D) treatment were used to remove functional characteristics of the EC. It is found that the EC played differential roles in modulating vascular tone and blood flow in distinct segments of arterioles. Impairment of the EC by L-D treatment significantly reduced both acetylcholine (Ach)-induced dilation and the local angiotensin conversion in small (4th order) arterioles (A4). Whereas, data obtained after inhibition of EDRF synthesis indicated that EDRF pathway appeared to be the dominant regulatory mechanism mediating agonists (e.g. Ach)-induced responses in these small vessels. In large (2nd order) arterioles (A2), on the other hand, neither L-D treatment nor EDRF inhibition affected Ach-induced dilation or local angiotensin conversion; therefore, these responses seemed to be independent of the EC or EDRF pathway. Autoregulation was observed in both A2 and A4 when perfusion flow (shear stress) and perfusion pressure (stretch) were elevated. Nevertheless, the underlying regulatory mechanisms in response to mechanical stimuli differed in these series-arranged arterioles. The EC/EDRF-dependent, flow-induced dilation was dominant in A2; whereas, the myogenic autoregulation (which appears to be independent of the EC) played major role in A4. Therefore, the function of the EC does not appear homogenous throughout the arteriolar portion of the microcirculation. Thus, the local control of blood flow and autoregulatory behavior in the microcirculation is distinctive at different levels of the vasculature; whereas, the differential role of the EC in discrete segments of series-arranged arterioles seems to be the determinant for these differences. These differential modulations of vascular tone and blood flow by the EC at discrete levels of the microcirculation may have important implications in pathological conditions, such as hypertension, diabetes, and atherosclerosis.
Subjects/Keywords: Anatomy and physiology; Animals; Biological sciences; Health and environmental sciences; Pharmacology; Anatomy; Animal Structures; Pharmacology
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❌
APA ·
Chicago ·
MLA ·
Vancouver ·
CSE |
Export
to Zotero / EndNote / Reference
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APA (6th Edition):
Tang, T. (1994). Differential Role of the Endothelium in Regulating Microvascular Blood Flow. (Doctoral Dissertation). East Tennessee State University. Retrieved from https://dc.etsu.edu/etd/2802
Chicago Manual of Style (16th Edition):
Tang, Tao. “Differential Role of the Endothelium in Regulating Microvascular Blood Flow.” 1994. Doctoral Dissertation, East Tennessee State University. Accessed December 06, 2019.
https://dc.etsu.edu/etd/2802.
MLA Handbook (7th Edition):
Tang, Tao. “Differential Role of the Endothelium in Regulating Microvascular Blood Flow.” 1994. Web. 06 Dec 2019.
Vancouver:
Tang T. Differential Role of the Endothelium in Regulating Microvascular Blood Flow. [Internet] [Doctoral dissertation]. East Tennessee State University; 1994. [cited 2019 Dec 06].
Available from: https://dc.etsu.edu/etd/2802.
Council of Science Editors:
Tang T. Differential Role of the Endothelium in Regulating Microvascular Blood Flow. [Doctoral Dissertation]. East Tennessee State University; 1994. Available from: https://dc.etsu.edu/etd/2802

East Tennessee State University
23.
Wang, Kening.
Changes in Intracellular Chloride During Osmotic Stress and L-alanine Uptake in Mouse Hepatocytes.
Degree: PhD, Biomedical Sciences, 1992, East Tennessee State University
URL: https://dc.etsu.edu/etd/2821
► A stable intracellular ionic environment is necessary for hepatocytes to function normally. Thus, during hypotonic shock or L-alanine uptake, hepatocytes swell and then exhibit…
(more)
▼ A stable intracellular ionic environment is necessary for hepatocytes to function normally. Thus, during hypotonic shock or L-alanine uptake, hepatocytes swell and then exhibit a regulatory volume decrease (RVD), which comprises an increase in K+ conductance (G K), an increased K+ efflux, and a hyperpolarization of transmembrane potential (V m). Since hepatocyte intracellular Cl- has been demonstrated to distribute passively with V m, this study is designed to test the hypothesis that the hypotonic shock- or L-alanine uptake-induced hyperpolarization of V m might provide an electromotive force for the efflux of hepatocyte intracellular Cl-, which in turn would contribute osmotically to the RVD in hepatocytes. Double-barreled ion-selective microelectrodes were used to measure the changes of hepatocyte transmembrane potential, intracellular ionic activities (especially intracellular Cl- activity, (a i Cl)), and intracellular water volume during either anisotonic stress or L-alanine uptake. Hepatocyte V m hyperpolarized, (a i Cl) decreased, intracellular K+ activity (a i K) decreased, and intracellular water volume increased during hyposmotic stress. When perfused with L-alanine, hepatocyte V m exhibited a transient depolarization followed by repolarization and then underwent a constant hyperpolarization. Meanwhile, hepatocyte intracellular Na+ activity (a i Na) increased, a i K & a i Cl decreased, and intracellular water volume increased. In both hypotonic shock and L-alanine uptake conditions, the decreased a i K could be attributed to cell swelling. However, the decrease in a i Cl was greater than could be accounted for by cell swelling. When the change of V m was inhibited by K+ channel blockers, the change of a i Cl was also inhibited. Based on the measured a i Cl, Cl- was always at its electrochemical equilibrium in all of the control and experimental conditions. The conclusions of this study emphasize the passive distribution of hepatocyte intracellular Cl- with the changes of V m induced by hypotonic stress and L-alanine uptake. Thus, the data strongly support the idea that the hypotonic shock- or L-alanine uptake-induced hyperpolarization of V m provides electromotive force for the efflux of hepatocyte intracellular Cl-. This could contribute to hepatocyte volume regulation during both hypotonic shock and organic solute transport.
Subjects/Keywords: Alanine uptake; Anatomy and physiology; Animals; Biological sciences; Cellular biology; Anatomy; Animal Structures; Cell Biology
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APA ·
Chicago ·
MLA ·
Vancouver ·
CSE |
Export
to Zotero / EndNote / Reference
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APA (6th Edition):
Wang, K. (1992). Changes in Intracellular Chloride During Osmotic Stress and L-alanine Uptake in Mouse Hepatocytes. (Doctoral Dissertation). East Tennessee State University. Retrieved from https://dc.etsu.edu/etd/2821
Chicago Manual of Style (16th Edition):
Wang, Kening. “Changes in Intracellular Chloride During Osmotic Stress and L-alanine Uptake in Mouse Hepatocytes.” 1992. Doctoral Dissertation, East Tennessee State University. Accessed December 06, 2019.
https://dc.etsu.edu/etd/2821.
MLA Handbook (7th Edition):
Wang, Kening. “Changes in Intracellular Chloride During Osmotic Stress and L-alanine Uptake in Mouse Hepatocytes.” 1992. Web. 06 Dec 2019.
Vancouver:
Wang K. Changes in Intracellular Chloride During Osmotic Stress and L-alanine Uptake in Mouse Hepatocytes. [Internet] [Doctoral dissertation]. East Tennessee State University; 1992. [cited 2019 Dec 06].
Available from: https://dc.etsu.edu/etd/2821.
Council of Science Editors:
Wang K. Changes in Intracellular Chloride During Osmotic Stress and L-alanine Uptake in Mouse Hepatocytes. [Doctoral Dissertation]. East Tennessee State University; 1992. Available from: https://dc.etsu.edu/etd/2821

East Tennessee State University
24.
Chen, Yuejin.
Characterization of the Vasoactivity of Tachykinins in Isolated Rat Kidney: Functional Studies and in Vitro Receptor Autoradiography.
Degree: PhD, Biomedical Sciences, 1994, East Tennessee State University
URL: https://dc.etsu.edu/etd/2892
► Although tachykinins have potent vascular actions, their effect on renal resistance blood vessels is currently unknown. The vasoactive properties of tachykinins and related analogs…
(more)
▼ Although tachykinins have potent vascular actions, their effect on renal resistance blood vessels is currently unknown. The vasoactive properties of tachykinins and related analogs were assessed in isolated perfused rat kidney. At a basal perfusion pressure (PP) of 75 ± 6 mm Hg (n = 5), bolus injections of substance P (SP) had no significant vasoactive effect. Following a sustained increase in baseline PP (134 ± 10 mm Hg) produced by phenylephrine (1 μM), SP evoked a dose-dependent increase in PP. The largest dose of SP increased PP by 60 ± 5 mm Hg. The vasoconstrictor response to SP was not blocked by phentolamine when angiotensin II was used to increase basal tone. Thus, the response to SP is not mediated by norepinephrine. Pressor responses to SP were not potentiated by peptidase inhibitors, captopril and thiorphan. SP(1-7) had no effect on PP, suggesting that the pressor response to SP is C-terminal dependent and tachykinin receptor mediated. The selective NK-1 receptor agonist, (Sar9,Met(O2)11]SP, had no effect on PP. In contrast, both the selective NK-2 and NK-3 receptor agonists, GR-64349 and (MePhe7) NKB, produced dose-dependent pressor responses (116 ± 8 and 134 ± 15 mm Hg increases in PP at 33 nmol, respectively) and were more potent than SP. Infusion of capsaicin (500 nM) produced an initial increase in PP following by a more prolonged decrease in PP. Clamping the renal vein produced a marked increase in PP. The localization of NK-3 receptors in rat kidney evaluated by film autoradiography using 125I- (MePhe7]NKB revealed a high density of specific binding sites on the proximal ureter and renal pelvis, moderate density in the renal vein and its large branches, and a low density in the inner strip of outer medulla, but no specific binding on the renal artery system and cortex. High resolution autoradiograms demonstrated 125I- (MePhe7]NKB binding sites on the tunica media of the renal vein and tunica muscularises of renal pelvis and ureter. Specific binding of 125I-BHSP was found in association with the renal artery and renal pelvis. No specific SP binding sites were associated with renal vein. These data indicate that the pressor effect of tachykinins in the isolated rat kidney can be mediated by NK-2 and/or NK-3 receptors. The latter may be on the vascular smooth muscle of the renal vein.
Subjects/Keywords: Anatomy and physiology; Animals; Biological sciences; Biophysics; Health and environmental sciences; Pharmacology; Vasoactive; Anatomy; Animal Structures; Biophysics; Pharmacology
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❌
APA ·
Chicago ·
MLA ·
Vancouver ·
CSE |
Export
to Zotero / EndNote / Reference
Manager
APA (6th Edition):
Chen, Y. (1994). Characterization of the Vasoactivity of Tachykinins in Isolated Rat Kidney: Functional Studies and in Vitro Receptor Autoradiography. (Doctoral Dissertation). East Tennessee State University. Retrieved from https://dc.etsu.edu/etd/2892
Chicago Manual of Style (16th Edition):
Chen, Yuejin. “Characterization of the Vasoactivity of Tachykinins in Isolated Rat Kidney: Functional Studies and in Vitro Receptor Autoradiography.” 1994. Doctoral Dissertation, East Tennessee State University. Accessed December 06, 2019.
https://dc.etsu.edu/etd/2892.
MLA Handbook (7th Edition):
Chen, Yuejin. “Characterization of the Vasoactivity of Tachykinins in Isolated Rat Kidney: Functional Studies and in Vitro Receptor Autoradiography.” 1994. Web. 06 Dec 2019.
Vancouver:
Chen Y. Characterization of the Vasoactivity of Tachykinins in Isolated Rat Kidney: Functional Studies and in Vitro Receptor Autoradiography. [Internet] [Doctoral dissertation]. East Tennessee State University; 1994. [cited 2019 Dec 06].
Available from: https://dc.etsu.edu/etd/2892.
Council of Science Editors:
Chen Y. Characterization of the Vasoactivity of Tachykinins in Isolated Rat Kidney: Functional Studies and in Vitro Receptor Autoradiography. [Doctoral Dissertation]. East Tennessee State University; 1994. Available from: https://dc.etsu.edu/etd/2892

East Tennessee State University
25.
Cheng, Hong.
Quantal Mechanisms Underlying Stimulation-induced Augmentation and Potentiation.
Degree: PhD, Biomedical Sciences, 1998, East Tennessee State University
URL: https://dc.etsu.edu/etd/2893
► Repetitive stimulation of motor nerves causes an increase in the number of packets of transmitter ("quanta") that can be released in the ensuing period.…
(more)
▼ Repetitive stimulation of motor nerves causes an increase in the number of packets of transmitter ("quanta") that can be released in the ensuing period. This represents a type of conditioning, in which synaptic transmission may be enhanced by prior activity. Despite many studies of this phenomenon, there have been no investigations of the quantal mechanisms underlying these events, due to the rapid changes in transmitter output and the short time periods involved. To examine this problem, a method was developed in which estimates of the quantal release parameters could be obtained over very brief periods (3 s). Conventional microelectrode techniques were used to record miniature endplate potentials (MEPPs) from isolated frog (Rana pipiens) cutaneous pectoris muscles, before and after repetitive (40 sec at 80 Hz) nerve stimulation. Estimates were obtained of m (number of quanta released), n (number of functional release sites), p (mean probability of release) and varsp (spatial variance in p) using a method that employs counts of MEPPs per unit time. Fluctuations in the estimates were reduced using a moving bin technique (bin size = 3 s, Δbin = 1 s). Muscle contraction was prevented using low Ca2+, high Mg2+ Ringer or normal Ringer to which μ-conotoxin GIIIA was added. These studies showed that: (1) the post-stimulation increase in transmitter release was dependent on stimulation frequency and not on the total number of stimulus impulses. When the total number of pulses was kept constant, the high frequency pattern produced a higher level of transmitter release than did the lower frequency patterns; (2) augmentation and potentiation were present in both low Ca2+, high Mg2+ and normal Ringer solutions, but potentiation, m, n, p and varsp were greater in normal Ringer solution than in low Ca2+, high Mg2+ solution. In low Ca2+, high Mg2+ solution, there was a larger decrease in n compared to p; (3) hypertonicity (addition of 100 mM sucrose) produced a marked increase in both basal and stimulation-induced values of m, n, and p. By contrast, there was a marked increase in the stimulation-induced but not the basal values of varsp; (4) hypertonicity produced a decrease in augmentation but had no effect on potentiation; (5) augmentation and potentiation appeared to involve mitochondrial uptake and efflux of cytoplasmic Ca2+. Tetraphenylphosphonium (which blocks mitochondrial Ca2+ efflux and uptake) decreased augmentation and potentiation in low Ca2+, high Mg2+ solutions but increased potentiation in the same solution made hypertonic with 100 mM sucrose; (6) the overall findings suggest that this new method may be useful for investigating the subcellular dynamics of transmitter release following nerve stimulation.
Subjects/Keywords: Anatomy and physiology; Animals; Augmentation; Biological sciences; Hypertonicity; Miniature endplate potentials; Neurology; Potentiation; Quantal mechanisms; Stimulation-induced; Anatomy; Animal Structures; Neurology
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❌
APA ·
Chicago ·
MLA ·
Vancouver ·
CSE |
Export
to Zotero / EndNote / Reference
Manager
APA (6th Edition):
Cheng, H. (1998). Quantal Mechanisms Underlying Stimulation-induced Augmentation and Potentiation. (Doctoral Dissertation). East Tennessee State University. Retrieved from https://dc.etsu.edu/etd/2893
Chicago Manual of Style (16th Edition):
Cheng, Hong. “Quantal Mechanisms Underlying Stimulation-induced Augmentation and Potentiation.” 1998. Doctoral Dissertation, East Tennessee State University. Accessed December 06, 2019.
https://dc.etsu.edu/etd/2893.
MLA Handbook (7th Edition):
Cheng, Hong. “Quantal Mechanisms Underlying Stimulation-induced Augmentation and Potentiation.” 1998. Web. 06 Dec 2019.
Vancouver:
Cheng H. Quantal Mechanisms Underlying Stimulation-induced Augmentation and Potentiation. [Internet] [Doctoral dissertation]. East Tennessee State University; 1998. [cited 2019 Dec 06].
Available from: https://dc.etsu.edu/etd/2893.
Council of Science Editors:
Cheng H. Quantal Mechanisms Underlying Stimulation-induced Augmentation and Potentiation. [Doctoral Dissertation]. East Tennessee State University; 1998. Available from: https://dc.etsu.edu/etd/2893

East Tennessee State University
26.
King, Judy A.
Adaptation of Striped Bass to Sea Water Following Direct Transfer from Freshwater: Morphological, Biochemical, and Physiological Parameters.
Degree: PhD, Biomedical Sciences, 1987, East Tennessee State University
URL: https://dc.etsu.edu/etd/2932
► There has been heightened interest in the biology of striped bass (Morone saxatilis) because of increased pollution in their native spawning grounds and because…
(more)
▼ There has been heightened interest in the biology of striped bass (Morone saxatilis) because of increased pollution in their native spawning grounds and because of their extensive use in landlocked sport fisheries. Their euryhalinity makes them an excellent species for osmoregulation studies. The objective of this research was to study the rate of adaptation of striped bass gills to sea water (3% salt) after direct transfer from freshwater using biochemical (ion transport enzyme levels), physiological (chloride efflux), and ultrastructural methods. Striped bass have specialized osmoregulatory cells located on the interlamellar and afferent surfaces of their gill filaments as shown by light microscopy (LM), transmission electron microscopy (TEM), and scanning electron microscopy (SEM). SEM studies show that apical pit (opening of one or more chloride cells) morphology changes during sea water adaptation, and the number of apical pits increases by 32.5% after two weeks in sea water. Chloride cell size and number, extent of basolateral tubular system, and number of mitochondria per chloride cell appear to increase upon adaptation to sea water. Sodium-potassium adenosine triphosphatase (Na,K-ATPase) activity is maximal on day 3 after transfer to sea water. Studies suggest that cortisol may act as a hormonal mediator for long term adaptation to sea water. The general morphology of both freshwater and sea water adapted fish gills were studied. Preliminary studies indicate that the osmium-dimethylsulfoxide-osmium method can be used to investigate intracellular structural changes in striped bass gills. Since the chloride cells are associated with the afferent surface of the filament, the blood supply to that area is also of great interest in osmoregulation studies. Studies of the gill vasculature using corrosion casting (i.e. filling blood vessels with plastic resins) and SEM indicate that the blood vessel distribution in the striped bass gill is similar to that of other euryhaline species with arterio-arterial, arterio-venous, and nutritive pathways. Blood flow may be controlled at a variety of places by sphincters, shunts and cellular contraction. Correlation of these biochemical, physiological and anatomical measurements will aid in the understanding of the process of adaptation to sea water. (Abstract shortened with permission of author.)
Subjects/Keywords: Anatomy and physiology; Aquaculture; Biological sciences; Biology; Fish production; Zoology; Anatomy; Aquaculture and Fisheries; Biology; Physiology; Zoology
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APA ·
Chicago ·
MLA ·
Vancouver ·
CSE |
Export
to Zotero / EndNote / Reference
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APA (6th Edition):
King, J. A. (1987). Adaptation of Striped Bass to Sea Water Following Direct Transfer from Freshwater: Morphological, Biochemical, and Physiological Parameters. (Doctoral Dissertation). East Tennessee State University. Retrieved from https://dc.etsu.edu/etd/2932
Chicago Manual of Style (16th Edition):
King, Judy A. “Adaptation of Striped Bass to Sea Water Following Direct Transfer from Freshwater: Morphological, Biochemical, and Physiological Parameters.” 1987. Doctoral Dissertation, East Tennessee State University. Accessed December 06, 2019.
https://dc.etsu.edu/etd/2932.
MLA Handbook (7th Edition):
King, Judy A. “Adaptation of Striped Bass to Sea Water Following Direct Transfer from Freshwater: Morphological, Biochemical, and Physiological Parameters.” 1987. Web. 06 Dec 2019.
Vancouver:
King JA. Adaptation of Striped Bass to Sea Water Following Direct Transfer from Freshwater: Morphological, Biochemical, and Physiological Parameters. [Internet] [Doctoral dissertation]. East Tennessee State University; 1987. [cited 2019 Dec 06].
Available from: https://dc.etsu.edu/etd/2932.
Council of Science Editors:
King JA. Adaptation of Striped Bass to Sea Water Following Direct Transfer from Freshwater: Morphological, Biochemical, and Physiological Parameters. [Doctoral Dissertation]. East Tennessee State University; 1987. Available from: https://dc.etsu.edu/etd/2932

University of California – San Francisco
27.
Behonick, Danielle Janine.
A Study of MMPs During Skeletal Development and Repair.
Degree: Biomedical Sciences, 2007, University of California – San Francisco
URL: http://www.escholarship.org/uc/item/2qs377z5
► The extracellular matrix (ECM) is an essential player in functions including cell survival, migration and differentiation. It is a dynamic reflection of the state of…
(more)
▼ The extracellular matrix (ECM) is an essential player in functions including cell survival, migration and differentiation. It is a dynamic reflection of the state of a tissue, both responding to and directing the behavior of local cells. The remodeling of this matrix is a common method of regulating local cell behaviors and as such, molecules involved in this remodeling process are integral to proper development as well as the prevention of disease states. The matrix metalloproteinases (MMPs) are a family of zinc-dependent cysteine proteinases collectively able to cleave all known ECM proteins. Many members of this family act in concert to provide the degradative activity required during a variety of physiological processes. Skeletal development occurs by two distinct mechanisms: intramembranous and endochondral ossification. Intramembranous ossification results from direct differentiation of mesenchymal precursors into osteoblasts, and is restricted to the clavicle and the bones of the skull. The skeletal elements of the rib cage, spinal column and limbs are formed by endochondral ossification, wherein cartilaginous templates are remodeled into mature, mineralized skeletal elements. The process of fetal skeletal development is largely recapitulated during skeletal repair: many cell types, molecules and mechanisms are held in common by these processes. MMPs are critical in promoting proper skeletal development and repair in a variety of settings. The studies described in this dissertation have contributed to our understanding of the roles of several MMPs during the processes of skeletal development and repair. In particular, this work demonstrates the importance of MMP13 (collagenase-3) for chondrocyte resorption and bone remodeling during endochondral bone development as well as repair by both endochondral and intramembranous ossification.
Subjects/Keywords: Biology, Anatomy; Biology, Cell; MMP; collagen; chondrocyte; osteoblast; skeletal development; fracture repair
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APA ·
Chicago ·
MLA ·
Vancouver ·
CSE |
Export
to Zotero / EndNote / Reference
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APA (6th Edition):
Behonick, D. J. (2007). A Study of MMPs During Skeletal Development and Repair. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/2qs377z5
Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
Chicago Manual of Style (16th Edition):
Behonick, Danielle Janine. “A Study of MMPs During Skeletal Development and Repair.” 2007. Thesis, University of California – San Francisco. Accessed December 06, 2019.
http://www.escholarship.org/uc/item/2qs377z5.
Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
MLA Handbook (7th Edition):
Behonick, Danielle Janine. “A Study of MMPs During Skeletal Development and Repair.” 2007. Web. 06 Dec 2019.
Vancouver:
Behonick DJ. A Study of MMPs During Skeletal Development and Repair. [Internet] [Thesis]. University of California – San Francisco; 2007. [cited 2019 Dec 06].
Available from: http://www.escholarship.org/uc/item/2qs377z5.
Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
Council of Science Editors:
Behonick DJ. A Study of MMPs During Skeletal Development and Repair. [Thesis]. University of California – San Francisco; 2007. Available from: http://www.escholarship.org/uc/item/2qs377z5
Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

East Tennessee State University
28.
Long, Tessa L.
In Vitro Assessment of the Toxicity of Cocaine and Its Metabolites in the Human Umbilical Artery.
Degree: PhD, Biomedical Sciences, 1998, East Tennessee State University
URL: https://dc.etsu.edu/etd/2941
► An in vitro model was used to assess the effect of cocaine and its metabolites on the umbilical artery. Objectives were to pharmacologically confirm…
(more)
▼ An in vitro model was used to assess the effect of cocaine and its metabolites on the umbilical artery. Objectives were to pharmacologically confirm the presence of adrenergic innervation using tyramine, evaluate the ability of cocaine, benzoylecgonine, norcocaine and cocaethylene to potentiate vasoconstriction by serotonin and norepinephrine, examine the ability of ketanserin to block the enhanced vasoconstriction produced by cocaine, and determine displacement of 3 H-ketanserin by serotonin, norepinephrine, tyramine and mianserin. The vasoconstrictive effect of tyramine (100 μM) was enhanced in the presence of cocaine by 257%. Vasoconstrictive effects of serotonin and norepinephrine were significantly enhanced by cocaine by 28%, and 64% respectively; producing significant increases in the cumulative response. Norcocaine significantly augmented the maximum response to norepinephrine by 54%. Benzoylecgonine significantly decreased the maximum response to serotonin by 36% as well as the cumulative response. Ketanserin (0.03 μM) completely attenuated the vasoconstrictive potentiation of serotonin and norepinephrine by cocaine; shifting the EC50 for serotonin to the right 10-fold in the presence of ketanserin and cocaine. Ketanserin shifted the EC15 for norepinephrine with cocaine to the right 205-fold. Maximum response to norepinephrine with cocaine was depressed 54% by ketanserin. Serotonin, tyramine, and mianserin were able to displace 3 H-ketanserin (3 nM) from the membrane fraction of the human umbilical artery. Indicating that serotonin2 receptors are involved in vasoconstrictive responses to serotonin and tyramine. Norepinephrine did not displace 3 H-ketanserin in the membrane fraction of the umbilical artery. These data suggest that enhanced vasoconstriction of norepinephrine and serotonin by cocaine and potentiation of the maximum response to norepinephrine by norcocaine in the human umbilical artery may be important components of perinatal cocaine toxicity. Ketanserin was able to suppress the umbilical artery constriction produced by cocaine, demonstrating its antidotal potential. The potentiation of the tyramine response by cocaine and the displacement of 3 H-ketanserin by tyramine indicate that tyramine may be producing its vasoconstrictive effect through serotonin2 in the umbilical artery.
Subjects/Keywords: Anatomy and physiology; Animals; Biological sciences; Cocaine; Health and environmental sciences; Metabolites; Molecular biology; Toxicity; Toxicology; Umbilical artery; Anatomy; Animal Structures; Molecular Biology; Toxicology
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❌
APA ·
Chicago ·
MLA ·
Vancouver ·
CSE |
Export
to Zotero / EndNote / Reference
Manager
APA (6th Edition):
Long, T. L. (1998). In Vitro Assessment of the Toxicity of Cocaine and Its Metabolites in the Human Umbilical Artery. (Doctoral Dissertation). East Tennessee State University. Retrieved from https://dc.etsu.edu/etd/2941
Chicago Manual of Style (16th Edition):
Long, Tessa L. “In Vitro Assessment of the Toxicity of Cocaine and Its Metabolites in the Human Umbilical Artery.” 1998. Doctoral Dissertation, East Tennessee State University. Accessed December 06, 2019.
https://dc.etsu.edu/etd/2941.
MLA Handbook (7th Edition):
Long, Tessa L. “In Vitro Assessment of the Toxicity of Cocaine and Its Metabolites in the Human Umbilical Artery.” 1998. Web. 06 Dec 2019.
Vancouver:
Long TL. In Vitro Assessment of the Toxicity of Cocaine and Its Metabolites in the Human Umbilical Artery. [Internet] [Doctoral dissertation]. East Tennessee State University; 1998. [cited 2019 Dec 06].
Available from: https://dc.etsu.edu/etd/2941.
Council of Science Editors:
Long TL. In Vitro Assessment of the Toxicity of Cocaine and Its Metabolites in the Human Umbilical Artery. [Doctoral Dissertation]. East Tennessee State University; 1998. Available from: https://dc.etsu.edu/etd/2941

East Tennessee State University
29.
Mabe, Abigail Marie.
Characterization of Murine Cardiac Cholinergic Innervation and Its Remodeling in Type 1 Diabetes.
Degree: PhD, Biomedical Sciences, 2008, East Tennessee State University
URL: https://dc.etsu.edu/etd/2009
► Murine models have become increasingly popular to study various aspects of cardiovascular diseases due to their ease of genetic manipulation. Unfortunately, there has been…
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▼ Murine models have become increasingly popular to study various aspects of cardiovascular diseases due to their ease of genetic manipulation. Unfortunately, there has been little effort put into describing the distribution of autonomic nerves in the mouse heart, making it difficult to compare current findings from clinical and experimental models related to cardiovascular diseases. Furthermore, determination of the requirements for the development of this system and its maintenance in adult mice remains largely unexplored. This study represents the first detailed mapping of cholinergic neuroanatomy of the mouse heart based on immunohistochemical staining using true cholinergic markers. We found cholinergic innervation of the mouse heart to be largely focused in the atrium and conducting system. We investigated the involvement of the neurotrophic factor neurturin (NRTN) in the development of cholinergic innervation, because there was indirect evidence that implicated it as a crucial factor. Results from our work definitively demonstrate that NRTN plays a major role in the development of cardiac parasympathetic ganglia and cholinergic innervation of the mouse heart. Adult NRTN knockout mice exhibited a drastic reduction in the number of intracardiac neurons with decreased atrial acetylcholine, cholinergic nerve density at the sinoatrial node and negative chronotropic responses to vagal stimulation. The presence of NRTN and its receptors in hearts from adult wild-type mice suggests that this neurotrophic factor might also be required for maintenance of cardiac cholinergic innervation. Finally, we wanted to determine how intracardiac neurons and their processes change during diseased states, specifically type 1 diabetes. This work has shown that the cardiac cholinergic nervous system in the mouse undergoes structural and functional remodeling when challenged with streptozotocin-induced diabetes. Cholinergic nerves in diabetic hearts undergo extensive sprouting at the sinoatrial node with no change in the number of intracardiac neurons. Cholinergic function appears to be enhanced in diabetic mice, based on pharmacological testing, despite decreased response to direct vagal nerve stimulation. Evidence also suggests that diabetic mice have an imbalance in autonomic control of heart rate. The latter findings suggest that disruption of central input into intrinsic cardiac ganglia also contributes to the neuropathology of type 1 diabetes.
Subjects/Keywords: neurotrophic factor; parasympathetic; intrinsic cardiac neuron; autonomic nervous system; streptozotocin; diabetes; Anatomy; Cardiovascular System; Medicine and Health Sciences; Nervous System
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APA (6th Edition):
Mabe, A. M. (2008). Characterization of Murine Cardiac Cholinergic Innervation and Its Remodeling in Type 1 Diabetes. (Doctoral Dissertation). East Tennessee State University. Retrieved from https://dc.etsu.edu/etd/2009
Chicago Manual of Style (16th Edition):
Mabe, Abigail Marie. “Characterization of Murine Cardiac Cholinergic Innervation and Its Remodeling in Type 1 Diabetes.” 2008. Doctoral Dissertation, East Tennessee State University. Accessed December 06, 2019.
https://dc.etsu.edu/etd/2009.
MLA Handbook (7th Edition):
Mabe, Abigail Marie. “Characterization of Murine Cardiac Cholinergic Innervation and Its Remodeling in Type 1 Diabetes.” 2008. Web. 06 Dec 2019.
Vancouver:
Mabe AM. Characterization of Murine Cardiac Cholinergic Innervation and Its Remodeling in Type 1 Diabetes. [Internet] [Doctoral dissertation]. East Tennessee State University; 2008. [cited 2019 Dec 06].
Available from: https://dc.etsu.edu/etd/2009.
Council of Science Editors:
Mabe AM. Characterization of Murine Cardiac Cholinergic Innervation and Its Remodeling in Type 1 Diabetes. [Doctoral Dissertation]. East Tennessee State University; 2008. Available from: https://dc.etsu.edu/etd/2009

Stellenbosch University
30.
Van Wyk, Christine.
Ancillary methods to improve diagnostic accuracy of thyroid nodules on fine-needle aspiration cytology smears.
Degree: MScMed (Dept. of Biomedical Sciences. Anatomy and Histology, Biomedical Sciences, 2007, Stellenbosch University
URL: http://hdl.handle.net/10019.1/2749
► Thyroid nodules are a common clinical problem encountered by physicians, surgeons and radiologists who deal with the head and neck region. However, most follicular lesions…
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▼ Thyroid nodules are a common clinical problem encountered by physicians, surgeons and radiologists who deal with the head and neck region. However, most follicular lesions of the thyroid are benign, so that the indications for surgery should be as accurate as possible. The morphological difficulty on fine-needle aspiration biopsy (FNAB) of reliably distinguishing preoperatively between benign and malignant lesions has led to a search for ancillary methods that can assist with the diagnosis.
The aim of the first study was to develop a cytological scoring system to improve diagnostic accuracy of fine-needle aspiration biopsy of papillary carcinomas with special reference to the follicular variant of papillary carcinoma. The objective of the second study was the application of immunodiagnostic markers Galectin-3 and HBME-1 to histology tissue sections and their corresponding fine-needle aspiration cytology smears to assess their value in distinguishing benign from malignant thyroid lesions.
In the first study 16 different cytological features such as background, architecture and cellular morphology were quantatively assessed and scored. Only 14 of the 16 variables were statistically significant. The statistical analysis demonstrated that a score ≥ 4 was indicative of a papillary carcinoma with a sensitivity of 96%. A score < 4 suggested a benign multinodular goiter with a specificity of 97%.
In the second study Galectin-3 and HBME-1 were applied to histology tissue sections and their corresponding fine-needle aspiration cytology smears. Statistical analyses showed that the sensitivity of immunohistochemistry for diagnosing malignancy was better than the immunocytochemistry, but the specificity of immunocytochemistry was superior. Furthermore the diagnostic accuracy of immunohistochemistry (86%) and immunocytochemistry (88%) using co-expression of these two antibodies was excellent. In this study on immunocytochemistry, papillary carcinomas were clearly identified with a 100% co-expression in the classic and 71% in the follicular variant of papillary carcinoma. For the surgeon the identification of papillary carcinoma is critical, as this determines the extent of surgery. Similary, the confirmation of a non-neoplastic lesion may prevent surgery. In most cases follicular neoplasms, benign or malignant, will usually be excised for histopathology, prior to definite therapy.
These studies show that the implementation of ancillary methods such as a scoring system and immunodiagnostic markers can improve the diagnostic accuracy of thyroid fine-needle aspiration biopsies in our laboratory. This may lead to better management of thyroid nodules. However, it is advisable that cytopathologists always take all the clinical features and image analyses into consideration before making a diagnosis.
Advisors/Committee Members: Louw, Mercia, Wright, Colleen, University of Stellenbosch. Faculty of Health Sciences. Dept. of Biomedical Sciences. Anatomy and Histology..
Subjects/Keywords: Anatomy and histology; Thyroid gland – Cytology – Technique; Thyroid gland – Histology; Thyroid gland – Needle biopsy – Technique
Record Details
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Record Details
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❌
APA ·
Chicago ·
MLA ·
Vancouver ·
CSE |
Export
to Zotero / EndNote / Reference
Manager
APA (6th Edition):
Van Wyk, C. (2007). Ancillary methods to improve diagnostic accuracy of thyroid nodules on fine-needle aspiration cytology smears. (Masters Thesis). Stellenbosch University. Retrieved from http://hdl.handle.net/10019.1/2749
Chicago Manual of Style (16th Edition):
Van Wyk, Christine. “Ancillary methods to improve diagnostic accuracy of thyroid nodules on fine-needle aspiration cytology smears.” 2007. Masters Thesis, Stellenbosch University. Accessed December 06, 2019.
http://hdl.handle.net/10019.1/2749.
MLA Handbook (7th Edition):
Van Wyk, Christine. “Ancillary methods to improve diagnostic accuracy of thyroid nodules on fine-needle aspiration cytology smears.” 2007. Web. 06 Dec 2019.
Vancouver:
Van Wyk C. Ancillary methods to improve diagnostic accuracy of thyroid nodules on fine-needle aspiration cytology smears. [Internet] [Masters thesis]. Stellenbosch University; 2007. [cited 2019 Dec 06].
Available from: http://hdl.handle.net/10019.1/2749.
Council of Science Editors:
Van Wyk C. Ancillary methods to improve diagnostic accuracy of thyroid nodules on fine-needle aspiration cytology smears. [Masters Thesis]. Stellenbosch University; 2007. Available from: http://hdl.handle.net/10019.1/2749
.