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Several reports indicate that hypoglycemic sulfonylureas augment Ca(2+)-dependent insulin secretion via mechanisms other than inhibition of the ATP-sensitive K(+) channel. The effect involves a 65-kd protein in the granule membrane and culminates in intragranular acidification. Lowering of granule pH is necessary for the insulin granule to gain release competence. Proton pumping into the granule is driven by a v-type H(+)-ATPase, but requires simultaneous Cl(-) uptake into the granule via metabolically regulated ClC-3 Cl(-) channels to maintain electroneutrality. Here we discuss the possibility that modulation of granule ClC-3 channels represents the mechanism whereby sulfonylureas directly potentiate the beta-cell exocytotic machinery.

Original publication

DOI

10.2337/diabetes.51.2007.s33

Type

Conference paper

Publication Date

02/2002

Volume

51 Suppl 1

Pages

S33 - S36

Keywords

Adenosine Triphosphate, Chloride Channels, Exocytosis, Insulin, Insulin Secretion, Islets of Langerhans, Potassium Channels, Sulfonylurea Compounds