Champion H C, Wang R, Santiago J A, Murphy W A, Coy D H, Kadowitz P J, Hellstrom W J
Department of Urology, Tulane University School of Medicine, New Orleans, Louisiana 70112, USA.
J Androl. 1997 Sep-Oct;18(5):513-21.
The purpose of the present study was to investigate the effects of intracavernosal injections of adrenomedullin (ADM) and calcitonin gene-related peptide (CGRP), two structurally similar peptides, on penile erection in the anesthetized cat. Erectile responses to ADM and CGRP were compared with responses to a standard drug combination (1.65 mg papaverine, 25 microg phentolamine, and 0.5 microg prostaglandin E1 [PGE1]). Intracavernosal injections of ADM (0.1-3 nmol) and CGRP (0.01-0.3 nmol) induced erection in a dose-dependent manner. The maximal increase in intracavernosal pressure in response to ADM was a 75% increase, while the maximal response to CGRP was comparable to that induced by the reference combination, and the maximal increase in penile length was comparable with ADM, CGRP, and the standard drug combination. The duration of the maximal pressure increase and the total duration of the response to ADM and CGRP were more abbreviated than with the control combination, and systemic blood pressure was reduced significantly after administration of CGRP, the control combination, and the higher doses of ADM. The nitric oxide synthase inhibitor, L-NAME, and the K+(ATP)-channel antagonist, glybenclamide, had no effect on the erectile response to CGRP or ADM. The CGRP receptor antagonist CGRP(8-37) attenuated the erectile response to CGRP but not to ADM. These data suggest that the erectile responses to ADM and CGRP are not mediated by nitric oxide release or the opening of K+(ATP) channels, two mechanisms reported to be involved in penile erection, and that CGRP and ADM induce penile erection by activating different receptors.
本研究的目的是探讨向海绵体内注射肾上腺髓质素(ADM)和降钙素基因相关肽(CGRP)这两种结构相似的肽对麻醉猫阴茎勃起的影响。将对ADM和CGRP的勃起反应与对标准药物组合(1.65 mg罂粟碱、25 μg酚妥拉明和0.5 μg前列腺素E1 [PGE1])的反应进行比较。向海绵体内注射ADM(0.1 - 3 nmol)和CGRP(0.01 - 0.3 nmol)以剂量依赖性方式诱导勃起。对ADM反应的海绵体内压最大增加为75%,而对CGRP的最大反应与参考组合诱导的反应相当,阴茎长度的最大增加与ADM、CGRP和标准药物组合相当。最大压力增加的持续时间以及对ADM和CGRP反应的总持续时间比对照组合更短,并且在给予CGRP、对照组合和较高剂量的ADM后,全身血压显著降低。一氧化氮合酶抑制剂L - NAME和钾离子(ATP)通道拮抗剂格列本脲对CGRP或ADM的勃起反应没有影响。CGRP受体拮抗剂CGRP(8 - 37)减弱了对CGRP的勃起反应,但对ADM没有影响。这些数据表明,对ADM和CGRP的勃起反应不是由一氧化氮释放或钾离子(ATP)通道开放介导的,这两种机制据报道参与阴茎勃起,并且CGRP和ADM通过激活不同的受体诱导阴茎勃起。