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二磷酸腺苷作为胰岛素分泌的细胞内调节因子。

Adenosine diphosphate as an intracellular regulator of insulin secretion.

作者信息

Nichols C G, Shyng S L, Nestorowicz A, Glaser B, Clement J P, Gonzalez G, Aguilar-Bryan L, Permutt M A, Bryan J

机构信息

Department of Cell Biology, Washington University School of Medicine, St. Louis, Missouri 63110, USA.

出版信息

Science. 1996 Jun 21;272(5269):1785-7. doi: 10.1126/science.272.5269.1785.

Abstract

Adenosine triphosphate (ATP)-sensitive potassium (KATP) channels couple the cellular metabolic state to electrical activity and are a critical link between blood glucose concentration and pancreatic insulin secretion. A mutation in the second nucleotide-binding fold (NBF2) of the sulfonylurea receptor (SUR) of an individual diagnosed with persistent hyperinsulinemic hypoglycemia of infancy generated KATP channels that could be opened by diazoxide but not in response to metabolic inhibition. The hamster SUR, containing the analogous mutation, had normal ATP sensitivity, but unlike wild-type channels, inhibition by ATP was not antagonized by adenosine diphosphate (ADP). Additional mutations in NBF2 resulted in the same phenotype, whereas an equivalent mutation in NBF1 showed normal sensitivity to MgADP. Thus, by binding to SUR NBF2 and antagonizing ATP inhibition of KATP++ channels, intracellular MgADP may regulate insulin secretion.

摘要

三磷酸腺苷(ATP)敏感性钾(KATP)通道将细胞代谢状态与电活动联系起来,是血糖浓度与胰腺胰岛素分泌之间的关键环节。一名被诊断为婴儿持续性高胰岛素性低血糖症的个体,其磺脲类受体(SUR)的第二个核苷酸结合结构域(NBF2)发生突变,产生的KATP通道可被二氮嗪打开,但对代谢抑制无反应。含有类似突变的仓鼠SUR具有正常的ATP敏感性,但与野生型通道不同,ATP的抑制作用不受二磷酸腺苷(ADP)拮抗。NBF2中的其他突变导致相同的表型,而NBF1中的等效突变对MgADP表现出正常敏感性。因此,通过与SUR NBF2结合并拮抗ATP对KATP++通道的抑制作用,细胞内MgADP可能调节胰岛素分泌。

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