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Rho激酶抑制剂(S)-(+)-2-甲基-1- [(4-甲基-5-异喹啉基)磺酰基]高哌嗪(H-1152)对大鼠阴茎的勃起促进作用。

Proerectile effects of the Rho-kinase inhibitor (S)-(+)-2-methyl-1-[(4-methyl-5-isoquinolinyl)sulfonyl]homopiperazine (H-1152) in the rat penis.

作者信息

Teixeira Cleber E, Ying Zhekang, Webb R Clinton

机构信息

Department of Physiology, Medical College of Georgia, 1120 15th St., CA-3101, Augusta, GA 30912-3000, USA.

出版信息

J Pharmacol Exp Ther. 2005 Oct;315(1):155-62. doi: 10.1124/jpet.105.086041. Epub 2005 Jun 23.

Abstract

The Rho-kinase pathway mediates Ca2+ sensitization in the penile circulation, which maintains the penis in the flaccid state. We aimed to investigate the functional effect of a novel Rho-kinase inhibitor, H-1152 [(S)-(+)-2-methyl-1-[(4-methyl-5-isoquinolinyl)sulfonyl]homopiperazine], both in vitro and in vivo as well as to demonstrate the expression of Rho guanine nucleotide exchange factors (RhoGEFs) in the rat corpus cavernosum (CC), by using a semiquantitative reverse transcription-polymerase chain reaction assay to measure their mRNA expression. Cumulative addition of H-1152 (0.001-3 microM) or Y-27632 [0.01-30 microM; (R)-(+)-trans-N-(4-pyridyl)-4-(1-aminoethyl)-cyclohexanecarboxamide] caused sustained relaxations of precontracted CC strips, which were not affected by inhibition of the nitric oxide signaling pathway. Addition of H-1152 (0.1 microM), Y-27632 (1 microM), or sodium nitroprusside (SNP; 0.1 microM) caused rightward shifts in the curves to phenylephrine (PE), but it had little effect on the contractions mediated by electrical field stimulation (EFS). It is noteworthy that when H-1152 or Y-27632 was combined with SNP, a marked synergistic inhibition was noted both on PE- and EFS-induced contractions. Intraperitoneal administration of H-1152 (100 nmol/kg) had a discrete effect on mean arterial pressure and significantly enhanced erectile responses evoked by stimulation of the cavernous nerve. The mRNA expression for PDZ-RhoGEF, p115RhoGEF, and leukemia-associated RhoGEF in cavernosal segments was visualized by electrophoresis on agarose gel. The results indicate that H-1152 is a powerful Rho-kinase inhibitor, giving rise to its therapeutic potential in the treatment of erectile dysfunction. The regulator of G-protein signaling-containing RhoGEFs may represent key components of the molecular mechanisms associated with the abnormal function of the cavernosal smooth muscle.

摘要

Rho激酶途径介导阴茎循环中的Ca2+致敏作用,从而使阴茎维持在疲软状态。我们旨在研究新型Rho激酶抑制剂H-1152 [(S)-(+)-2-甲基-1-[(4-甲基-5-异喹啉基)磺酰基]高哌嗪] 在体外和体内的功能作用,并通过半定量逆转录-聚合酶链反应测定法检测Rho鸟嘌呤核苷酸交换因子(RhoGEFs)在大鼠海绵体(CC)中的表达,以测量它们的mRNA表达。累积添加H-1152(0.001 - 3 microM)或Y-27632 [0.01 - 30 microM;(R)-(+)-反式-N-(4-吡啶基)-4-(1-氨基乙基)-环己烷甲酰胺] 可使预收缩的CC条带持续松弛,这不受一氧化氮信号通路抑制的影响。添加H-1152(0.1 microM)、Y-27632(1 microM)或硝普钠(SNP;0.1 microM)会使去氧肾上腺素(PE)的曲线向右移动,但对电场刺激(EFS)介导的收缩作用很小。值得注意的是,当H-1152或Y-27632与SNP联合使用时,对PE和EFS诱导的收缩均有明显的协同抑制作用。腹腔注射H-1152(100 nmol/kg)对平均动脉压有离散作用,并显著增强海绵体神经刺激诱发的勃起反应。通过琼脂糖凝胶电泳观察海绵体节段中PDZ-RhoGEF、p115RhoGEF和白血病相关RhoGEF的mRNA表达。结果表明,H-1152是一种强大的Rho激酶抑制剂,在治疗勃起功能障碍方面具有治疗潜力。含RhoGEFs的G蛋白信号调节剂可能代表与海绵体平滑肌功能异常相关的分子机制的关键组成部分。

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