The proposed project will enhance our understanding of the events which regulate stimulus-secretion coupling in pancreatic acinar cells. Advantage will be taken of the principal investigator's recent observation that the secretion of digestive enzymes by the mouse pancreas under certain conditions and in response to certain stimuli is inhibited after ingestion of an ethionine-containing diet. For example, in-vivo but not in-vitro basal secretion is reduced after exposure to an ethionine-containing diet. Furthermore, even in-vitro secretion is not totally normal in samples taken from ethionine-fed mice. Under these conditions, CCK-PZ and bethanechol induced secretion is inhibited although calcium ionophore (A-23187) induced secretion is not reduced. In the proposed studies, the effects of an ethionine-containing diet on several of the events believed to couple neurohormonal stimulation with the secretory response will be characterized. Basal, CCK-PZ, cholenergic and ionophore-stimulated secretion will be studied. Hormone binding, Ca2+ fluxes, protein carboxyl methylation, phosphatidyl inositol turnover, and phosphatidic acid generation will be measured. Parallel ethionine-induced effects on the event being studied and the secretory response will support the concept that the two processes are causally linked while divergent effects will indicate that the two are not causally linked. Thus, these studies will clarify the sequence of events which couple stimulus to secretion in the mouse pancreas and identify the mechanism by which this process in inhibited after ingestion of an ethionine-containing diet.

Project Start
1983-06-01
Project End
1986-08-31
Budget Start
1985-09-01
Budget End
1986-08-31
Support Year
3
Fiscal Year
1985
Total Cost
Indirect Cost
Name
Beth Israel Deaconess Medical Center
Department
Type
DUNS #
076593722
City
Boston
State
MA
Country
United States
Zip Code
Hirano, T; Saluja, A; Ramarao, P et al. (1992) Effects of chloroquine and methylamine on lysosomal enzyme secretion by rat pancreas. Am J Physiol 262:G439-44
Steer, M L (1992) Pathobiology of experimental acute pancreatitis. Yale J Biol Med 65:421-30;discussion 437-40
Printz, H; Saluja, A; Leli, U et al. (1990) Effects of hemorrhagic shock, aspirin, and ethanol on secretagogue-induced experimental pancreatitis. Int J Pancreatol 6:207-17
Leli, U; Saluja, A; Picard, L et al. (1990) Effects of a choline-deficient ethionine-supplemented diet on phospholipase C activity in mouse pancreatic acinar cell membranes and in electropermeabilized mouse pancreatic acini. J Pharmacol Exp Ther 253:847-50
Saluja, A K; Saluja, M; Printz, H et al. (1989) Experimental pancreatitis is mediated by low-affinity cholecystokinin receptors that inhibit digestive enzyme secretion. Proc Natl Acad Sci U S A 86:8968-71
Saluja, A K; Powers, R E; Steer, M L (1989) Inositol trisphosphate independent increase of intracellular free calcium and amylase secretion in pancreatic acini. Biochem Biophys Res Commun 164:8-13
Ohshio, G; Saluja, A K; Leli, U et al. (1989) Esterase inhibitors prevent lysosomal enzyme redistribution in two noninvasive models of experimental pancreatitis. Gastroenterology 96:853-9
Rutledge, P L; Saluja, A; Leli, U et al. (1988) A simple and efficient method of measuring in vitro amylase secretion by dispersed pancreatic acini. Pancreas 3:508-11
Saluja, A; Hashimoto, S; Saluja, M et al. (1987) Subcellular redistribution of lysosomal enzymes during caerulein-induced pancreatitis. Am J Physiol 253:G508-16
Saito, I; Hashimoto, S; Saluja, A et al. (1987) Intracellular transport of pancreatic zymogens during caerulein supramaximal stimulation. Am J Physiol 253:G517-26

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