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

机译:猪降钙素基因相关肽(CGRP)的分离,分子表征及其在猪胰腺中的内分泌作用。

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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.
机译:这项研究的目的是调查猪降钙素基因相关肽(CGRP)在调节内分泌猪胰腺中的可能作用。最初,我们从猪肾上腺和胰腺提取物中分离和纯化了CGRP。在两个组织中发现了肽的单一分子形式。对肾上腺肽进行测序,发现在六个位置不同于人α-CGRP,在三个位置不同于人β-CGRP。通过免疫组织化学,在胰腺神经节的神经纤维中发现了CGRP。猪肽的合成复制品以不同的剂量水平(10(-10),10(-9)和10(-8)M)注入分离的灌注猪胰腺中。灌流液中含5 mmol / L葡萄糖。 CGRP在10(-10)和10(-9)M时增加了胰岛素和胰高血糖素的分泌,而10(-8)M时则观察到了显着的下降。生长激素抑制素的分泌在10(-8)M CGRP下显着增加。在使用高亲和力的生长抑素抗体的免疫中和研究(n = 6)中,CGRP在10(-8)M的抑制作用被逆转为对胰岛素和胰高血糖素分泌的显着刺激。 CGRP剂量依赖性地抑制了响应方波的胰岛素分泌,葡萄糖浓度增加至11 mM。在10(-8)M时,胰岛素输出减少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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