Amylase release from dissociated mouse pancreatic acinar cells stimulated by glucagon: effect of membrane stabilizers.

1. The effect of membrane stabilizers and cytochalasin‐B on amylase secretion, basal and induced by ionophore A23187, CCK‐PZ, bethanechol and glucagon, was studied in dissociated mouse pancreatic acinar cells. 2. Cytochalasin‐B did not affect basal or secretagogue‐stimulated amylase secretion. 3. Membrane stabilizers [thymol (10(‐7)‐10(‐4) M), chlorpromazine (10(‐7)‐10(‐4) M) and propranolol (10(‐7)‐10(‐5) M) did not alter basal release of amylase. At higher concentrations of thymol (10(‐3) M), chlorpromazine (10(‐3) M) and propranolol (10(‐4) M), dissociated acinar cells were lysed as indicated by an increase in release of lactic dehydrogenase (LDH). 4. Ionophore A23187, CCK‐PZ (maximal effective concentrations, 0.01 u. ml.‐1), bethanechol (maximal effective concentrations, 10(‐4) M) and glucagon increased amylase secretion in a dose‐dependent fashion. Concentrations of CCK‐PZ and bethanechol beyond optimal levels decreased amylase secretion. Concentrations of ionophore A23187 and glucagon when tested beyond 10(‐6) M and 10(‐4) M respectively increased the release of LDH. In concentrations that were non‐toxic, membrane stabilizers blocked the stimulating effect of cholecystokinin‐pancreozymin and bethanechol on amylase secretion but did not alter the response to A23187 and glucagon. 5. Unlike bethanechol, glucagon neither increased the uptake of 45Ca nor did it alter the release of 45Ca from cells previously loaded with 45CaCl2. 6. These data provide evidence that stimulus‐secretion coupling in dissociated pancreatic acinar cells is basically similar to cells in situ. The effect of glucagon is consistent with the model in which hormone‐dependent mobilization of Ca2+ from intra‐ or extracellular sources is bypassed leading to digestive enzyme secretion.