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人源和大鼠源α-CGRP(降钙素基因相关肽)而非降钙素可引起大鼠肠系膜血管舒张。

Human and rat alpha-CGRP but not calcitonin cause mesenteric vasodilatation in rats.

作者信息

Marshall I, Al-Kazwini S J, Holman J J, Craig R K

出版信息

Eur J Pharmacol. 1986 Apr 16;123(2):217-22. doi: 10.1016/0014-2999(86)90662-x.

Abstract

A single gene encodes both calcitonin and the calcitonin gene-related peptide (CGRP). Human and rat alpha-CGRP were compared with sodium nitroprusside in the rat and rabbit isolated mesenteric vascular preparation perfused at constant flow. In the presence of the vasoconstrictor noradrenaline (10(-5) M), rat alpha-CGRP was about 10 times as potent as either human alpha-CGRP or sodium nitroprusside as a vasodilator in the rat mesenteric vasculature. In the rabbit mesenteric vasculature the order of potency was rat alpha-CGRP greater than human alpha-CGRP greater than sodium nitroprusside. Human and salmon calcitonin showed no vasodilator activity at doses 100 times greater than human alpha-CGRP. These results show that human and rat alpha-CGRP are potent vasodilators in the mesenteric vasculature, an effect not mimicked by the alternative gene product, the plasma calcium lowering hormone calcitonin.

摘要

单一基因编码降钙素和降钙素基因相关肽(CGRP)。将人和大鼠的α-CGRP与硝普钠在恒流灌注的大鼠和兔离体肠系膜血管制备物中进行比较。在存在血管收缩剂去甲肾上腺素(10^(-5) M)的情况下,在大鼠肠系膜血管系统中,大鼠α-CGRP作为血管舒张剂的效力约为人α-CGRP或硝普钠的10倍。在兔肠系膜血管系统中,效力顺序为大鼠α-CGRP>人α-CGRP>硝普钠。人降钙素和鲑鱼降钙素在剂量比人α-CGRP大100倍时未显示血管舒张活性。这些结果表明,人和大鼠的α-CGRP在肠系膜血管系统中是有效的血管舒张剂,而作为另一基因产物的血浆钙降低激素降钙素则没有这种作用。

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