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促胰岛素激素胰高血糖素样肽-I(7-37)对胰岛素瘤β TC-1细胞中胰岛素原基因表达和胰岛素原生物合成的刺激作用。

Insulinotropic hormone glucagon-like peptide-I(7-37) stimulation of proinsulin gene expression and proinsulin biosynthesis in insulinoma beta TC-1 cells.

作者信息

Fehmann H C, Habener J F

机构信息

Laboratory of Molecular Endocrinology, Massachusetts General Hospital, Howard Hughes Medical Institute, Harvard Medical School, Boston 02114.

出版信息

Endocrinology. 1992 Jan;130(1):159-66. doi: 10.1210/endo.130.1.1309325.

Abstract

Glucagon-like peptide-I(7-37) [GLP-I(7-37)] is an intestinal peptide hormone that is released in response to oral nutrients and that potently augments glucose-mediated insulin secretion. GLP-I(7-37) has potent insulin-releasing activities in vivo in response to oral nutrients, in situ in the isolated perfused pancreas, and in vitro in cultured pancreatic B-cells. As such GLP-I(7-37) is a potent hormonal mediator in the enteroinsular axis involved in the regulation of glucose homeostasis. We now show that in addition to stimulating the release of insulin, GLP-I(7-37) stimulates proinsulin gene expression at the levels of gene transcription and cellular levels of proinsulin messenger RNA as well as the translational biosynthesis of proinsulin. These findings of the positive anabolic actions of GLP-I(7-37) on the synthesis of insulin in B-cells support the notion that GLP-I(7-37) may be of therapeutic use in stimulating the production of insulin in patients with noninsulin-dependent diabetes mellitus and that overproduction of insulin with subsequent hypoglycemia will not occur in response to the administration of GLP-I(7-37). Furthermore, these positive actions of GLP-I(7-37) on insulin production obviate the possibility of B-cell exhaustion in response to such a potent secretagogue.

摘要

胰高血糖素样肽 -I(7 - 37)[GLP -I(7 - 37)]是一种肠道肽激素,它会在口服营养物质后释放,并能显著增强葡萄糖介导的胰岛素分泌。GLP -I(7 - 37)在体内对口服营养物质、在离体灌注胰腺原位以及在培养的胰腺β细胞体外实验中均具有强大的胰岛素释放活性。因此,GLP -I(7 - 37)是肠胰岛轴中参与调节葡萄糖稳态的一种强大的激素介质。我们现在表明,除了刺激胰岛素释放外,GLP -I(7 - 37)还在基因转录水平和胰岛素原信使核糖核酸的细胞水平以及胰岛素原的翻译生物合成水平上刺激胰岛素原基因表达。这些关于GLP -I(7 - 37)对β细胞胰岛素合成具有积极合成代谢作用的发现支持了这样一种观点,即GLP -I(7 - 37)可能在刺激非胰岛素依赖型糖尿病患者胰岛素产生方面具有治疗用途,并且给予GLP -I(7 - 37)不会导致胰岛素过量产生及随后的低血糖。此外,GLP -I(7 - 37)对胰岛素产生的这些积极作用排除了因这种强效促分泌剂导致β细胞耗竭的可能性。

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