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二氮嗪通过抵消钙离子内流来消除葡萄糖对胰岛素释放的抑制作用。

Diazoxide unmasks glucose inhibition of insulin release by counteracting entry of Ca2+.

作者信息

Bergsten P, Gylfe E, Wesslén N, Hellman B

机构信息

Department of Medical Cell Biology, University of Uppsala, Sweden.

出版信息

Am J Physiol. 1988 Oct;255(4 Pt 1):E422-7. doi: 10.1152/ajpendo.1988.255.4.E422.

Abstract

The interaction of diazoxide with the effects of glucose on the insulin-releasing mechanism was analyzed in beta-cell-rich pancreatic islets isolated from ob/ob mice. When added at a concentration of 400 microM to a medium containing 1.28 mM Ca2+, diazoxide converted glucose stimulation of insulin release into inhibition. Further addition of 2 mM theophylline restored the insulin secretory response to glucose. The paradoxical glucose inhibition of insulin release was accounted for by a diazoxide interaction with the entry of Ca2+, unmasking a capacity of the sugar to lower cytoplasmic Ca2+ below its resting concentration.

摘要

在从ob/ob小鼠分离出的富含β细胞的胰岛中,分析了二氮嗪与葡萄糖对胰岛素释放机制影响之间的相互作用。当以400微摩尔浓度添加到含有1.28毫摩尔钙离子的培养基中时,二氮嗪将葡萄糖对胰岛素释放的刺激转化为抑制作用。进一步添加2毫摩尔茶碱可恢复胰岛素对葡萄糖的分泌反应。胰岛素释放出现的反常的葡萄糖抑制作用是由于二氮嗪与钙离子内流相互作用,从而暴露出糖将细胞质钙离子浓度降低至静息浓度以下的能力。

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