Regulation of A- and B-Cell Function by Insulin and Glucagon
Wilfred Y. Fujimoto, J. Ensinck
Abstract
Wilfred Y. Fujimoto, J. Ensinck
Abstract
In monolayer cultures of pancreases from neonatal rats, glucagon added to the medium (5 or 50 ng/ml) stimulated insulin secretion. In contrast, exogenously added insulin (1.0 mU/ml) inhibited glucagon secretion when glucose was 1.7 or 5.5 mM, but not when glucose was 16.5 mM. This suggests that insulin may reduce glucagon release by enhancing glucose uptake by A-cells. Suppression of glucagon secretion by high glucose (16.5 mM) may be mediated by endogenously released insulin. These observations support the in vivo findings favoring a modulatory interaction between A- and B-cells.
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In monolayer cultures of pancreases from neonatal rats, glucagon added to the medium (5 or 50 ng/ml) stimulated insulin secretion. In contrast, exogenously added insulin (1.0 mU/ml) inhibited glucagon secretion when glucose was 1.7 or 5.5 mM, but not when glucose was 16.5 mM. This suggests that insulin may reduce glucagon release by enhancing glucose uptake by A-cells. Suppression of glucagon secretion by high glucose (16.5 mM) may be mediated by endogenously released insulin. These observations support the in vivo findings favoring a modulatory interaction between A- and B-cells.
Key concepts: Glucagon, Internal medicine, Endocrinology, Insulin, Secretion, In vivo, Chemistry, Pancreatic hormone