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一种Rho激酶抑制剂、可溶性鸟苷酸环化酶激活剂和释放一氧化氮的磷酸二酯酶5抑制剂:治疗勃起功能障碍的新方法。

A Rho-kinase inhibitor, soluble guanylate cyclase activator and nitric oxide-releasing PDE5 inhibitor: novel approaches to erectile dysfunction.

作者信息

Cellek Selim, Rees Rowland W, Kalsi Jas

机构信息

Wolfson Institute for Biomedical Research, University College London, Gower Street, Cruciform Building, London WC1E 6BT, UK.

出版信息

Expert Opin Investig Drugs. 2002 Nov;11(11):1563-73. doi: 10.1517/13543784.11.11.1563.

Abstract

Approximately 50% of men aged over 40 suffer from male erectile dysfunction. Treatment options have widened since the launch of the phosphodiesterase type 5 (PDE5) inhibitor, sildenafil citrate (Viagra trade mark ). However, a certain portion of the patient population, such as diabetics, do not gain significant benefit from PDE5 inhibitors, possibly due to a lack of endogenous nitric oxide. Therefore, new treatment modalities based on the absence of endogenous nitric oxide have been developed. Among them are Rho-kinase inhibitors, soluble guanylate cyclase activators and nitric oxide-releasing PDE5 inhibitors. The available data concerning these compounds will be summarised and their therapeutic potential for male erectile dysfunction will be discussed.

摘要

40岁以上的男性中,约50%患有男性勃起功能障碍。自磷酸二酯酶5型(PDE5)抑制剂枸橼酸西地那非(商品名伟哥)上市以来,治疗选择有所增加。然而,一部分患者群体,如糖尿病患者,无法从PDE5抑制剂中获得显著益处,这可能是由于内源性一氧化氮缺乏所致。因此,基于内源性一氧化氮缺乏的新治疗方式已被开发出来。其中包括Rho激酶抑制剂、可溶性鸟苷酸环化酶激活剂和释放一氧化氮的PDE5抑制剂。将总结关于这些化合物的现有数据,并讨论它们对男性勃起功能障碍的治疗潜力。

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