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Glucose and pharmacological modulators of ATP-sensitive K+ channels control [Ca2+]c by different mechanisms in isolated mouse alpha-cells

Authors :
UCL - MD/MNOP - Département de morphologie normale et pathologique
UCL - (SLuc) Service d'anatomie pathologique
UCL - MD/FSIO - Département de physiologie et pharmacologie
UCL - (SLuc) Service d'endocrinologie et de nutrition
Quoix, Nicolas
Cheng-Xue, Rui
Mattart, Laurine
Zeinoun, Ziad
Guiot, Yves
Beauvois, Mélanie C.
Henquin, Jean-Claude
Gilon, Patrick
UCL - MD/MNOP - Département de morphologie normale et pathologique
UCL - (SLuc) Service d'anatomie pathologique
UCL - MD/FSIO - Département de physiologie et pharmacologie
UCL - (SLuc) Service d'endocrinologie et de nutrition
Quoix, Nicolas
Cheng-Xue, Rui
Mattart, Laurine
Zeinoun, Ziad
Guiot, Yves
Beauvois, Mélanie C.
Henquin, Jean-Claude
Gilon, Patrick
Source :
Diabetes, Vol. 58, no. 2, p. 412-421 (2009)
Publication Year :
2009

Abstract

OBJECTIVE: We studied how glucose and ATP-sensitive K(+) (K(ATP)) channel modulators affect alpha-cell [Ca(2+)](c). RESEARCH DESIGN AND METHODS: GYY mice (expressing enhanced yellow fluorescent protein in alpha-cells) and NMRI mice were used. [Ca(2+)](c), the K(ATP) current (I(KATP), perforated mode) and cell metabolism [NAD(P)H fluorescence] were monitored in single alpha-cells and, for comparison, in single beta-cells. RESULTS: In 0.5 mmol/l glucose, [Ca(2+)](c) oscillated in some alpha-cells and was basal in the others. Increasing glucose to 15 mmol/l decreased [Ca(2+)](c) by approximately 30% in oscillating cells and was ineffective in the others. alpha-Cell I(KATP) was inhibited by tolbutamide and activated by diazoxide or the mitochondrial poison azide, as in beta-cells. Tolbutamide increased alpha-cell [Ca(2+)](c), whereas diazoxide and azide abolished [Ca(2+)](c) oscillations. Increasing glucose from 0.5 to 15 mmol/l did not change I(KATP) and NAD(P)H fluorescence in alpha-cells in contrast to beta-cells. The use of nimodipine showed that L-type Ca(2+) channels are the main conduits for Ca(2+) influx in alpha-cells. gamma-Aminobutyric acid and zinc did not decrease alpha-cell [Ca(2+)](c), and insulin, although lowering [Ca(2+)](c) very modestly, did not affect glucagon secretion. CONCLUSIONS: alpha-Cells display similarities with beta-cells: K(ATP) channels control Ca(2+) influx mainly through L-type Ca(2+) channels. However, alpha-cells have distinct features from beta-cells: Most K(ATP) channels are already closed at low glucose, glucose does not affect cell metabolism and I(KATP), and it slightly decreases [Ca(2+)](c). Hence, glucose and K(ATP) channel modulators exert distinct effects on alpha-cell [Ca(2+)](c). The direct small glucose-induced drop in alpha-cell [Ca(2+)](c) contributes likely only partly to the strong glucose-induced inhibition of glucagon secretion in islets.

Details

Database :
OAIster
Journal :
Diabetes, Vol. 58, no. 2, p. 412-421 (2009)
Notes :
English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1130578659
Document Type :
Electronic Resource