Miner Martin M, Seftel Allen D
Division of Biology and Medicine, Department of Family Medicine, Warren Alpert Medical School of Brown University, Providence, RI, USA.
Urol Clin North Am. 2007 Nov;34(4):483-96, v. doi: 10.1016/j.ucl.2007.08.008.
The development of pharmacologic therapy for erectile dysfunction (ED) has been possible because of incremental growth in our understanding of the physiology of normal erections and the complex pathophysiology of ED. Although the oral phosphodiesterase type 5 (PDE5) inhibitors have provided safe, effective treatment of ED for some men, a large proportion of men who have ED do not respond to PDE5 inhibitors or become less responsive or less satisfied as the duration of therapy increases. Also, men who are receiving organic nitrates and nitrates, such as amyl nitrate, cannot take PDE5 inhibitors because of nitrate interactions. The current options for treatment beyond PDE5 inhibitors are invasive, unappealing to some patients, and sometimes ineffective. The search for other options by which ED can be treated has branched out and now encompasses centrally acting mechanisms that control erectile function. Drugs available in Europe include apomorphine. This article focuses on the mechanism of centrally acting agents and reviews clinical data on potential new centrally acting drugs for men who have ED.
由于我们对正常勃起生理以及勃起功能障碍(ED)复杂病理生理的认识不断深入,勃起功能障碍的药物治疗得以发展。尽管口服5型磷酸二酯酶(PDE5)抑制剂为部分男性提供了安全、有效的ED治疗方法,但很大一部分患有ED的男性对PDE5抑制剂无反应,或者随着治疗时间的延长反应性降低或满意度下降。此外,正在接受有机硝酸盐和硝酸酯类药物(如亚硝酸异戊酯)治疗的男性,由于硝酸盐相互作用,不能服用PDE5抑制剂。目前,除PDE5抑制剂外的其他治疗选择具有侵入性,对一些患者缺乏吸引力,且有时无效。寻找其他治疗ED的方法已经展开,现在包括控制勃起功能的中枢作用机制。欧洲可用的药物包括阿扑吗啡。本文重点介绍中枢作用药物的机制,并综述针对患有ED的男性潜在新型中枢作用药物的临床数据。