Brain S D, Hughes S R, Cambridge H, O'Driscoll G
Division of Biomedical Sciences, King's College, London.
Agents Actions. 1993;38 Spec No:C19-21. doi: 10.1007/BF01991124.
The neuropeptide calcitonin gene-related peptide (CGRP) is a potent vasodilator in the microcirculation of many tissues including the skin and joint. In order to elucidate the mechanism of endogenous CGRP release, we have used a multiple site 133Xe clearance technique to measure local blood flow changes in response to agents injected intradermally in the rabbit. Capsaicin (100 nmol/site) and human alpha CGRP (3 pmol/site) stimulated similar increases in blood flow and, in both cases, the effect was totally abolished by the CGRP antagonist, CGRP8-37 (1 nmol/site). By contrast, the nitric oxide synthase inhibitor L-nitro arginine methyl ester (L-NAME, 30 nmol/site) had little effect on human alpha CGRP-induced vasodilation, but caused significant inhibition of the response to capsaicin (p < 0.05). These results show that increased blood flow in rabbit skin caused by exogenous CGRP is independent of nitric oxide. In addition, however, they suggest that nitric oxide is required for either the release of endogenous CGRP from capsaicin-sensitive nerves or its subsequent activity.
神经肽降钙素基因相关肽(CGRP)在包括皮肤和关节在内的许多组织的微循环中是一种强效血管扩张剂。为了阐明内源性CGRP释放的机制,我们使用了多部位133Xe清除技术来测量家兔皮内注射药物后局部血流的变化。辣椒素(100 nmol/部位)和人αCGRP(3 pmol/部位)刺激血流产生相似的增加,并且在这两种情况下,CGRP拮抗剂CGRP8 - 37(1 nmol/部位)完全消除了这种效应。相比之下,一氧化氮合酶抑制剂L - 硝基精氨酸甲酯(L - NAME,30 nmol/部位)对人αCGRP诱导的血管舒张几乎没有影响,但对辣椒素引起的反应有显著抑制作用(p < 0.05)。这些结果表明,外源性CGRP引起的家兔皮肤血流增加与一氧化氮无关。然而,此外,它们表明一氧化氮对于内源性CGRP从辣椒素敏感神经的释放或其随后的活性是必需的。