Affiliation:
1. Joslin Research Laboratory, Department of Medicine, Harvard Medical School, Peter Bent Brigham Hospital, The Joslin Diabetes Foundation, Inc. Boston, Massachusetts, and Departments of Medicine and Biochemistry, McMaster University, Hamilton Ontario, Canada
Abstract
Glucagon (1.7 × 10−9M) stimulated gluconeogenesis, ureogenesis, lactate production, ketogenesis, proteolysis and glycogenolysis in the isolated perfused rat liver. Insulin at relatively low concentrations (10-100 μU/ml.) suppressed these metabolic effects of glucagon. When a molar glucagon:insulin ratio (2.6 or 26) was selected, which partially suppressed the stimulatory effects of glucagon and the inhibitory effects of insulin, a 100-1,000 fold change in insulin and glucagon concentration at a constant glucagon:insulin ratio, did not alter the rate of gluconeogenesis, ketogenesis, ureogenesis, glycogenolysis or lactate production. These results indicate that glucagon and insulin are complete competative antagonists in the perfused liver. This suggests that it is the glucagon:insulin ratio and not the absolute concentration of either hormone that determines their metabolic events in liver.
Publisher
American Diabetes Association
Subject
Endocrinology, Diabetes and Metabolism,Internal Medicine
Cited by
149 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献