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猪降钙素基因相关肽(CGRP)的分离、分子特征及其在猪胰腺中的内分泌作用

Isolation and molecular characterization of porcine calcitonin gene-related peptide (CGRP) and its endocrine effects in the porcine pancreas.

作者信息

Rasmussen T N, Bersani M, Schmidt P, Thim L, Kofod H, Jørgensen P N, Poulsen S S, Holst J J

机构信息

Department of Medical Physiology, The Panum Institute, University of Copenhagen, Denmark.

出版信息

Pancreas. 1998 Mar;16(2):195-204. doi: 10.1097/00006676-199803000-00014.

Abstract

The aim of this study was to investigate the possible role of porcine calcitonin gene-related peptide (CGRP) in the regulation of the endocrine porcine pancreas. Initially, we isolated and purified CGRP from extracts of porcine adrenal glands and pancreases. A single molecular form of the peptide was found in the two tissues. The adrenal peptide was sequenced and found to differ from human alpha-CGRP at six positions and from human beta-CGRP at three positions. By immunohistochemistry, CGRP was found in nerve fibers in the pancreatic ganglia. A synthetic replica of the porcine peptide was infused at different dose levels (10(-10), 10(-9), and 10(-8) M) into isolated perfused porcine pancreata. With 5 mmol/L glucose in the perfusate. CGRP at 10(-10) and 10(-9) M increased insulin and glucagon secretion, whereas significant decreases were observed with 10(-8) M. Somatostatin secretion was increased significantly by 10(-8) M CGRP. In immunoneutralization studies (n = 6) using a high-affinity somatostatin antibody, the inhibitory effect of CGRP at 10(-8) M was reversed to a significant stimulation of insulin and glucagon secretion. Insulin secretion in response to square-wave increases in glucose concentration to 11 mM was inhibited dose dependently by CGRP; at 10(-8) M the insulin output decreased by 72+/-9% (n = 6). The present results indicate that CGRP may be involved in the regulation of insulin and glucagon secretion from the porcine pancreas.

摘要

本研究的目的是探讨猪降钙素基因相关肽(CGRP)在调节猪内分泌胰腺方面可能发挥的作用。最初,我们从猪肾上腺和胰腺提取物中分离并纯化了CGRP。在这两种组织中发现了该肽的单一分子形式。对肾上腺肽进行了测序,发现它与人类α-CGRP在六个位置不同,与人类β-CGRP在三个位置不同。通过免疫组织化学方法,在胰腺神经节的神经纤维中发现了CGRP。将猪肽的合成复制品以不同剂量水平(10^(-10)、10^(-9)和10^(-8) M)注入离体灌注的猪胰腺。灌注液中葡萄糖浓度为5 mmol/L时,10^(-10)和10^(-9) M的CGRP可增加胰岛素和胰高血糖素的分泌,而10^(-8) M时则观察到显著下降。10^(-8) M的CGRP可显著增加生长抑素的分泌。在使用高亲和力生长抑素抗体的免疫中和研究(n = 6)中,10^(-8) M的CGRP的抑制作用逆转,对胰岛素和胰高血糖素分泌产生显著刺激。CGRP对葡萄糖浓度方波增加至11 mM时的胰岛素分泌呈剂量依赖性抑制;在10^(-8) M时,胰岛素分泌量下降了72±9%(n = 6)。目前的结果表明,CGRP可能参与猪胰腺胰岛素和胰高血糖素分泌的调节。

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