Horm Metab Res 1971; 3(2): 65-70
DOI: 10.1055/s-0028-1095029
Originals

© Georg Thieme Verlag KG Stuttgart · New York

The Stimulus-Secretion Coupling of Glucose-Induced Insulin Release - II. Interaction of Alkali and Alkaline Earth Cations[*]

W. J. Malaisse , F.  Malaisse-Lagae , G.  Brisson
  • Laboratories of Experimental Medicine and Anatomo-Pathology, Brussels University, Brussels, Belgium
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Publication History

Publication Date:
07 January 2009 (online)

Abstract

Glucose-induced insulin secretion is enhanced at high K+ concentrations (10 to 34 mEq/l), and in the presence of ouabain. It is reduced when Na+ is partially replaced by either Li+, Tris, or larger amounts of K+(87 to 115 mEq/l). The elevated rate of secretion observed at high K+ concentration (24 mEq/l) is markedly reduced by replacement of NaCl by sucrose. These data suggest that Na+ entry in the beta-cell favors insulin release. However, the stimulant action of glucose is increased when Na+ is replaced by choline and persists in a Na+-free medium, indicating that the influx of Na+ per se is not necessary for secretion to occur. It is suggested that alkali cations could influence insulin secretion through an altered handling of alkaline earth cations by the beta-cell. In favor of this hypothesis, it is shown that the beta-cell becomes unresponsive to Ba++ when Na+ is replaced by Li+, Tris, or large amounts of K+; whereas the elevated rates of secretion observed when Na+ is replaced by choline or moderate amounts of K+ are markedly reduced by the omission of Ca++ from the incubation medium. The inhibitory effect of extracellular acidosis upon glucose-induced secretion could also be due, in part at least, to a reduced entry of Ca++ in the beta-cell. These data support the concept that entry of Ca++ might trigger the release of insulin and that the influence of alkali cations upon insulin release could be mediated by an alteration of this process.

1 This work was supported in part by a grant from the Fonds National de la Recherche Scientifique (Brussels, Belgium) and a grant-in-aid from the Lilly Research Laboratories (Indianapolis, Indiana).

1 This work was supported in part by a grant from the Fonds National de la Recherche Scientifique (Brussels, Belgium) and a grant-in-aid from the Lilly Research Laboratories (Indianapolis, Indiana).

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