Vitamin D and pancreatic islet function. II. Dynamics of insulin release and cationic fluxes

Pancreatic islets were prepared from control and vitamin D-deprived rats 2 or 5 weeks after weaning and, in the latter case, after 3 or 6 days treatment with exogenous vitamin D3 (60 nmol per day). The islets were prelabelled with both 86Rb and 45Ca and placed in a perfusion chamber. Vitamin D depri...

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Veröffentlicht in:Journal of endocrinological investigation 1988-09, Vol.11 (8), p.585-593
Hauptverfasser: Billaudel, B, Labriji-Mestaghanmi, H, Sutter, B C, Malaisse, W J
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container_issue 8
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container_title Journal of endocrinological investigation
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creator Billaudel, B
Labriji-Mestaghanmi, H
Sutter, B C
Malaisse, W J
description Pancreatic islets were prepared from control and vitamin D-deprived rats 2 or 5 weeks after weaning and, in the latter case, after 3 or 6 days treatment with exogenous vitamin D3 (60 nmol per day). The islets were prelabelled with both 86Rb and 45Ca and placed in a perfusion chamber. Vitamin D deprivation or administration failed to affect 86Rb outflow whether prior or after stimulation of the islets by a rise in either extracellular D-glucose or Ca2+ concentration. However, vitamin D deprivation decreased and vitamin D administration enhanced the basal 45Ca fractional outflow rate, as well as the magnitude of changes in both 45Ca and insulin release evoked by the rise in either D-glucose or extracellular Ca2+. It is proposed that the alteration in 45Ca fluxes and insulin release attributable to changes in the supply of vitamin D are, to a large extent, independent of the changes in nutrient catabolism conceivably associated with vitamin D deprivation and administration.
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subjects Animals
Calcium - pharmacokinetics
Calcium - pharmacology
Cations - pharmacokinetics
Glucose - pharmacology
Insulin - metabolism
Insulin Secretion
Islets of Langerhans - drug effects
Islets of Langerhans - physiology
Rats
Rubidium - pharmacokinetics
Rubidium - pharmacology
Vitamin D - pharmacology
title Vitamin D and pancreatic islet function. II. Dynamics of insulin release and cationic fluxes
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