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艾塞那肽-4是一种高效激动剂,而截短的艾塞那肽-(9 - 39)-酰胺是胰岛素分泌β细胞的胰高血糖素样肽1-(7 - 36)-酰胺受体的拮抗剂。

Exendin-4 is a high potency agonist and truncated exendin-(9-39)-amide an antagonist at the glucagon-like peptide 1-(7-36)-amide receptor of insulin-secreting beta-cells.

作者信息

Göke R, Fehmann H C, Linn T, Schmidt H, Krause M, Eng J, Göke B

机构信息

Department of Internal Medicine, Philipps University of Marburg, Germany.

出版信息

J Biol Chem. 1993 Sep 15;268(26):19650-5.

PMID:8396143
Abstract

Exendin-4 purified from Heloderma suspectum venom shows structural relationship to the important incretin hormone glucagon-like peptide 1-(7-36)-amide (GLP-1). We demonstrate that exendin-4 and truncated exendin-(9-39)-amide specifically interact with the GLP-1 receptor on insulinoma-derived cells and on lung membranes. Exendin-4 displaced 125I-GLP-1, and unlabeled GLP-1 displaced 125I-exendin-4 from the binding site at rat insulinoma-derived RINm5F cells. Exendin-4 had, like GLP-1, a pronounced effect on intracellular cAMP generation, which was reduced by exendin-(9-39)-amide. When combined, GLP-1 and exendin-4 showed additive action on cAMP. They each competed with the radio-labeled version of the other peptide in cross-linking experiments. The apparent molecular mass of the respective ligand-binding protein complex was 63,000 Da. Exendin-(9-39)-amide abolished the cross-linking of both peptides. Exendin-4, like GLP-1, stimulated dose dependently the glucose-induced insulin secretion in isolated rat islets, and, in mouse insulinoma beta TC-1 cells, both peptides stimulated the proinsulin gene expression at the level of transcription. Exendin-(9-39)-amide reduced these effects. In conclusion, exendin-4 is an agonist and exendin-(9-39)-amide is a specific GLP-1 receptor antagonist.

摘要

从希拉毒蜥毒液中纯化得到的艾塞那肽-4与重要的肠促胰岛素激素胰高血糖素样肽1-(7-36)-酰胺(GLP-1)存在结构关联。我们证明,艾塞那肽-4和截短的艾塞那肽-(9-39)-酰胺可特异性地与胰岛素瘤来源细胞及肺细胞膜上的GLP-1受体相互作用。在大鼠胰岛素瘤来源的RINm5F细胞中,艾塞那肽-4可取代125I-GLP-1,未标记的GLP-1也可从结合位点取代125I-艾塞那肽-4。与GLP-1一样,艾塞那肽-4对细胞内cAMP的生成有显著影响,而艾塞那肽-(9-39)-酰胺可降低这种影响。GLP-1和艾塞那肽-4联合使用时,对cAMP表现出相加作用。在交联实验中,它们各自与另一种肽的放射性标记版本相互竞争。各自配体结合蛋白复合物的表观分子量为63,000 Da。艾塞那肽-(9-39)-酰胺可消除两种肽的交联。与GLP-1一样,艾塞那肽-4可剂量依赖性地刺激分离的大鼠胰岛中葡萄糖诱导的胰岛素分泌,并且在小鼠胰岛素瘤βTC-1细胞中,两种肽均可在转录水平刺激胰岛素原基因表达。艾塞那肽-(9-39)-酰胺可降低这些作用。总之,艾塞那肽-4是一种激动剂,而艾塞那肽-(9-39)-酰胺是一种特异性GLP-1受体拮抗剂。

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