Electrolyte transport in the intestine of the common brushtail possum (Trichosurus vulpecula) differs from that observed in eutherian mammals. This study has used molecular physiology to identify and characterise the expression and distribution of membrane transporters potentially responsible for these differences in electrolyte transport in the possum intestine. In the possum ileum, secretagogues stimulate an electrogenic Cl⁻-independent HCO₃⁻ secretory response but secretagogue-stimulated Cl⁻ secretion does not occur in this tissue. Based on the ion dependence and pharmacology of the stimulated secretory response, the expression of the cystic fibrosis transmembrane conductance regulator (CFTR), pancreatic Na⁺ HCO₃⁻ cotransporter (pNBC) and Na⁺ K⁺ 2Cl⁻ cotransporter (NKCC1) were investigated in the ileum. Reverse transcription PCR experiments showed that CFTR, pNBC and NKCC1 mRNA transcripts were expressed in the ileal epithelium. It was then demonstrated by in situ hybridisation that both CFTR and pNBC were localised predominantly in the crypts and the levels of expression decreased along the crypt-villous axis towards the lumen. Significantly, the in situ hybridisation results showed that there were low levels of NKCC1 transcript in the ileal epithelium. Western blot studies confirmed that mature CFTR and pNBC proteins were expressed in the ileum, while NKCC1 protein was not detected. The findings of the present study suggest that the absence of Cl⁻ secretion in the ileum is because NKCC1 expression is not elevated in the epithelium. The expression of mature CFTR and pNBC protein suggest that these membrane transporters are involved in the stimulated electrogenic HCO₃⁻ secretory response. The evidence also suggests that CFTR may mediate HCO₃⁻ efflux in the ileum. In contrast, secretagogues do not stimulate an electrogenic secretory response in the proximal and distal colon. This study has shown that CFTR, NKCC1 and pNBC proteins are expressed in the proximal and distal colon. Both NKCC1 and pNBC transcripts were localised to the crypt base in the proximal colon. However, it was shown that CFTR has a punctate distribution and the transcript was predominantly observed in the upper crypt and surface cell region. This study indicated that NKCC1 and pNBC were distributed in a different region of the epithelium compared to CFTR. It was concluded that the distribution of these membrane transporters in different regions of the epithelium accounts for the absence of a stimulated electrogenic secretory response in the possum colon. Given that no stimulated electrogenic secretory response is observed in the colon, it is suggested that HCO₃⁻ secretion by the ileum may have an important physiological role in maintaining an appropriate fluid and pH composition for fermentation in the colonic lumen.

Errata pages inserted behind leaf 293. / Includes bibliography (leaves 255-293). / xv, 293, [60] leaves, [33] leaves of plates : ill. (some col.) ; 30 cm. / Title page, contents and abstract only. The complete thesis in print form is available from the University Library. / Aims to determine the molecular mechanism by which expression of Fas is lost in colorectal tumours and investigates the effects of re-introducing Fas into colon cancer cells. An animal study was undertaken in addition to the studies of colorectal cancer, to investigate the role of Fas signalling in hormone-dependent involution of the prostate gland. / Thesis (Ph.D.)--University of Adelaide, Dept. of Surgery, 1998?

Errata pages inserted behind leaf 293. / Includes bibliography (leaves 255-293). / xv, 293, [60] leaves, [33] leaves of plates : ill. (some col.) ; 30 cm. / Title page, contents and abstract only. The complete thesis in print form is available from the University Library. / Aims to determine the molecular mechanism by which expression of Fas is lost in colorectal tumours and investigates the effects of re-introducing Fas into colon cancer cells. An animal study was undertaken in addition to the studies of colorectal cancer, to investigate the role of Fas signalling in hormone-dependent involution of the prostate gland. / Thesis (Ph.D.)--University of Adelaide, Dept. of Surgery, 1998?

Introduction: Gastric and colon cancer are major causes of mortality and morbidity worldwide. Gastric cancer is often detected at an advanced stage and current chemotherapeutics are only modestly effective against this neoplasm. Novel chemotherapeutics, chemopreventive agents and treatment strategies are required to prevent and treat gastric cancer. The ideal method to eliminate cancer cells may be the induction of apoptosis, further preventing cell proliferation and tumour growth. Recently, short-chain fatty acids (SCFAs) butyrate and propionate have been investigated as potential chemotherapeutic agents, particularly in colon cancer. Butyrate is reported to induce apoptosis in colon cancer cells and is demonstrated to modulate intracellular redox state by altering the levels of an antioxidant, glutathione (GSH). GSH availability is controlled by the oxidative pentose pathway (OPP). Very few studies have investigated the effects of butyrate on cell types other than colon cancer cells, and even less is known regarding the effects of propionate. This thesis investigated the potential for SCFAs to induce apoptosis in a gastric cancer cell line, Kato III, compared to the colon cancer cell line, Caco-2. Cell cycle regulation, OPP activity, GSH availability and glucose metabolism were also assessed. Methods: Initial studies developed a new technique to measure 1-13C-D-glucose metabolism. Following this, Kato III and Caco-2 colon carcinoma cells were treated with butyrate or propionate (1mM, 5mM or 10mM) or a 5mM combination of both SCFAs. The induction of apoptosis and cell cycle alterations by these SCFAs were assessed using flow cytometry. OPP activity and GSH availability were assessed in both cell lines using colorimetric techniques. Butyrate metabolism was assessed using 13C-butyrate. Results: Butyrate and propionate significantly induced apoptosis and G2-M arrest in Kato III and Caco-2 cells, although to a significantly greater extent in the latter cell line. Moreover, butyrate induced apoptosis to a significantly greater extent than propionate, in both cell lines. SCFA treatment led to the significant up-regulation of OPP activity in both cancer cell lines while GSH availability was significantly reduced. Glucose metabolism was initially increased by all SCFA treatments, however, 72hr butyrate treatment led to its reduction. Importantly, glucose metabolism was measured using a new technique developed within this thesis. The rate of butyrate metabolism was demonstrated to correlate with the sensitivity of each cell line to this SCFA. Conclusions: This thesis provides evidence that SCFAs, particularly butyrate, induce apoptosis in gastric and colon cancer cells in vitro. The response of cancer cells to SCFAs appears complex, and involves multiple distinct mechanisms and pathways, including p53, Fas, changes to intracellular redox state and glucose metabolism. The capability of butyrate to induce apoptosis also appears to be directly related to the rate of its metabolism. Butyrate has the potential to be utilised as an adjunctive therapy for the treatment of gastric cancer and colon cancer. / Thesis (Ph.D.) -- School of Molecular and Biomedical Science, 2007

Thesis (Ph. D.)--University of Washington, 2007. / Vita. Includes bibliographical references (leaves 86-98).

Thesis (Ph. D.)--University of Adelaide, 1986. / Includes bibliographical references.

Thesis (Ph.D.)--University of Hong Kong, 2008. / Also available in print.

Thesis (Ph. D.)--University of Sydney, 2007. / Title from title screen (viewed Aug. 30, 2007). Submitted in fulfilment of the requirements for the degree of Doctor of Philosophy to the School of Public Health, Faculty of Medicine. Includes bibliography.

Thesis (Dr.P.H.)--University of Texas Health Science Center at Houston, School of Public Health, 2007. / Publication Number: AAT 3290041 Includes bibliographical references.

Thesis (Ph. D.)--University of Hong Kong, 2008. / Also available in print.