Y-27632, an inhibitor of Rho-kinase, antagonizes noradrenergic contractions in the rabbit and human penile corpus cavernosum

被引:85
作者
Rees, RW
Ralph, DJ
Royle, M
Moncada, S
Cellek, S
机构
[1] UCL, Wolfson Inst Biomed Res, London WC1E 6AE, England
[2] Middlesex Hosp, Inst Urol, London W1W 7EL, England
[3] Sussex Nuffield Hosp, Brighton BN2 6DX, E Sussex, England
关键词
contraction; Rho-kinase; corpus cavernosum; human; rabbit; Y-27632;
D O I
10.1038/sj.bjp.0704124
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
We have examined the effect of an inhibitor of Rho-kinase, (+)-(R)-trans-4-(1-aminoethyl)-N-(4-pyridyl) cyclohexanecarboxamide dihydrochloride monohydrate (Y-27632), on the contractions elicited by noradrenergic nerve stimulation and by phenylephrine in the human and rabbit penile corpus cavernosum. In both tissues, after treatment with scopolamine (10 muM) and N(G)-nitro-L-arginine methyl ester (L-NAME; 300 muM), electrical field stimulation (EFS) elicited noradrenergic contractions. These contractions were inhibited by Y-27632 in a concentration-dependent manner. The compound caused concentration-dependent relaxation of phenylephrine-contracted tissues, which were treated with scopolamine (10 muM), guanethidine (10 muM) and L-NAME (300 muM). These results suggest that Rho-kinase is involved in noradrenergic contractile pathway in the cavernosal smooth muscle of the penis.
引用
收藏
页码:455 / 458
页数:4
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