Affiliation:
1. Department of Medicine, Division of Endocrinology, Duke University Medical Center Durham, North Carolina 27706
Abstract
Five-hydroxytryptamine (serotonin) inhibited basal and stimulated insulin release from pieces of golden hamster pancreas. Five-hydroxyindole acetic acid was a less potent inhibitor of insulin release than was serotonin, while 5- hydroxytryptophan and tryptamine had no effect on this process. In contrast, L-tryptophan potentiated high glucosemediated insulin release. Thus there was an absolute structural requirement for a hydroxyl group in the five position of the indole ring, and a relative requirement for an amine group in the alkyl chain for these indole compounds to be inhibitors of insulin release. In further studies, methysergide maleate, a specific serotonin inhibitor, blocked this action of serotonin. Methysergide maleate also stimulated glucose-mediated insulin release suggesting that endogenous serotonin may influence in vitro insulin secretion. Thus the inhibitory effect of serotonin on insulin secretion appears to be quite specific.
Publisher
American Diabetes Association
Subject
Endocrinology, Diabetes and Metabolism,Internal Medicine
Cited by
39 articles.
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