We studied the effects of insulin and insulin secretagogues on pancreatic phospholipids and the release of amylase from pancreatic fragments incubated in vitro. Insulin provoked rapid, dose-related increases in amylase release, and these were accompanied by decreases in phosphatidylinositol and increases in phosphatidic acid. Glucose and other insulin secretagogues elicited similar changes in amylase release and pancreatic phospholipids; epinephrine blocked these effects of glucose, presumably via inhibition of glucose-induced insulin secretion. Effects of insulin and glucose on phospholipids and amylase release were dependent on Ca2+ in the incubation medium. These findings suggest that, in the pancreas, insulin enhances Ca2+-dependent phosphatidylinositol breakdown, which in turn influences amylase secretion. The effects of insulin on phospholipids may also explain certain other actions of insulin.
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Original contribution|
May 01 1981
Insulin and Its Secretagogues Activate Ca2+-dependent Phosphatidylinositol Breakdown and Amylase Secretion in Rat Pancreas In Vitro
Robert V Farese;
Robert V Farese
Veterans Administration Hospital and the Department of Medicine, University of South Florida College of Medicine
Tampa, Florida
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Ronald E Larson;
Ronald E Larson
Veterans Administration Hospital and the Department of Medicine, University of South Florida College of Medicine
Tampa, Florida
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Mohammad A Sabir
Mohammad A Sabir
Veterans Administration Hospital and the Department of Medicine, University of South Florida College of Medicine
Tampa, Florida
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Address reprint requests to Robert V. Farese, Veterans Administration Medical Center, 13000 North 30th Street, Tampa, Florida 33612.
Diabetes 1981;30(5):396–401
Article history
Received:
August 29 1980
Revision Received:
December 15 1980
Accepted:
December 15 1980
PubMed:
6164587
Citation
Robert V Farese, Ronald E Larson, Mohammad A Sabir; Insulin and Its Secretagogues Activate Ca2+-dependent Phosphatidylinositol Breakdown and Amylase Secretion in Rat Pancreas In Vitro. Diabetes 1 May 1981; 30 (5): 396–401. https://doi.org/10.2337/diab.30.5.396
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