Stimulation of insulin release by alpha-D-glucose pentaacetate

被引:38
作者
Malaisse, WJ [1 ]
Jijakli, H [1 ]
KAdiata, MM [1 ]
Sener, A [1 ]
Kirk, O [1 ]
机构
[1] NOVO NORDISK AS,DK-2880 BAGSVAERD,DENMARK
关键词
D O I
10.1006/bbrc.1997.6119
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Insulin release from rat pancreatic islets was stimulated by alpha-D-glucose pentaacetate (1.7 mM), but not by an equimolar concentration of beta-D-galactose pentaacetate. The secretory response to alpha-D-glucose pentaacetate was not reproduced by D-glucose and/or acetate, tested at concentrations equimolar to that of the hexose ester, and failed to be adversely affected by 3-O-methyl-D-glucose, even when used at a concentration sufficient to inhibit glucose-stimulated insulin release. These findings suggest that the insulinotropic action of alpha-D-glucose pentaacetate is attributable, in part at least, to the intracellular generation of D-glucose from the ester. The present work thus introduces selected esters of D-glucose as tools for the cellular supply of the hexose by a process that does apparently not involve its carrier-mediated transport across the plasma membrane. (C) 1997 Academic Press.
引用
收藏
页码:435 / 436
页数:2
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