Maggi C A, Chiba T, Giuliani S
Pharmacology Department, A. Menarini Pharmaceuticals, Florence, Italy.
Eur J Pharmacol. 1991 Jan 3;192(1):85-8. doi: 10.1016/0014-2999(91)90072-x.
The C-terminal fragment of the human alpha-calcitonin gene-related peptide (hCGRP), hCGRP-(8-37) competitively antagonized both the positive inotropic effect of hCGRP in the guinea-pig isolated left atria (pA2 6.89) and the smooth muscle relaxant effect of hCGRP in the rat isolated vas deferens (pA2 6.55) but left the response to isoprenaline unaffected in both preparations. In addition, hCGRP-(8-37) reduced the responses produced by activation of the 'efferent' function of capsaicin-sensitive primary afferents in both preparations thus providing pharmacological evidence for the involvement of endogenous CGRP. hCGRP-(8-37) appears a useful tool to establish the physiological role of CGRP in peripheral preparations from different species.
人α-降钙素基因相关肽(hCGRP)的C末端片段hCGRP-(8-37),能竞争性拮抗hCGRP对豚鼠离体左心房的正性肌力作用(pA2 6.89)以及对大鼠离体输精管的平滑肌舒张作用(pA2 6.55),但在这两种标本中,对异丙肾上腺素的反应未受影响。此外,hCGRP-(8-37)降低了两种标本中辣椒素敏感的初级传入神经“传出”功能激活所产生的反应,从而为内源性CGRP的参与提供了药理学证据。hCGRP-(8-37)似乎是确定CGRP在不同物种外周标本中的生理作用的有用工具。