Brain S D, Williams T J, Tippins J R, Morris H R, MacIntyre I
Nature. 1985;313(5997):54-6. doi: 10.1038/313054a0.
A novel peptide, calcitonin gene-related peptide (CGRP), has been predicted to result from alternative processing of the primary RNA transcript of the calcitonin gene in the rat. Several lines of evidence suggest that CGRP is a transmitter in the central and peripheral nervous system. Human CGRP has been isolated and characterized, and shown to have potent effects on the heart. The observations presented here indicate that human and rat CGRP also have potent effects on blood vessels. Intradermal injection of CGRP in femtomole doses induces microvascular dilatation resulting in increased blood flow, which we have detected in the rabbit by using a 133Xe clearance technique. In human skin, CGRP induces persistent local reddening. Microscopic observation of the hamster cheek pouch in vivo revealed that topical application of CGRP induces dilatation of arterioles. Furthermore, CGRP relaxes strips of rat aorta in vitro by an endothelial cell-dependent mechanism. Therefore, we suggest that local extravascular release of CGRP may be involved in the physiological control of blood flow and that circulating CGRP may contribute to hyperaemia in certain pathological conditions.
一种新的肽,降钙素基因相关肽(CGRP),据预测是由大鼠降钙素基因的初级RNA转录本经可变加工产生的。多条证据表明CGRP是中枢和外周神经系统中的一种递质。人CGRP已被分离和鉴定,并显示对心脏有强效作用。此处给出的观察结果表明,人和大鼠的CGRP对血管也有强效作用。以飞摩尔剂量皮内注射CGRP会诱导微血管扩张,导致血流量增加,我们已通过使用133Xe清除技术在兔身上检测到这一现象。在人体皮肤中,CGRP会诱导持续的局部发红。对仓鼠颊囊进行体内显微镜观察发现,局部应用CGRP会诱导小动脉扩张。此外,CGRP在体外通过一种依赖内皮细胞的机制使大鼠主动脉条松弛。因此,我们认为CGRP在血管外局部释放可能参与了血流的生理控制,并且循环中的CGRP可能在某些病理状态下导致充血。