Department of Obstetrics and Gynaecology, Yong Loo Lin School of Medicine, National University Hospital, National University of Singapore, Singapore.
J Sex Med. 2011 Jul;8(7):1853-64. doi: 10.1111/j.1743-6109.2011.02279.x. Epub 2011 Apr 14.
The current pharmacotherapy for erectile dysfunction (ED) relies significantly on the use of phosphodiesterase type 5 (PDE5) inhibitors, but quite a proportion of ED patients are resistant to this therapy, necessitating a search for an alternative treatment. We reviewed available published data to analyze current evidence of hydrogen sulfide (H(2) S) as a novel pharmacotherapeutic agent with supportive role in sexual function.
To discuss the role of H(2) S in erectile function, its possible mechanism of action, and how this knowledge may be exploited for therapeutic use.
Pubmed and Medline search was conducted to identify original articles and reviews.
Data from peer-reviewed publications.
Animal studies using different species, including in vitro study done in humans, show evidence of H(2) S's pro-erectile effects. The mechanism behind is still unclear, but evidence in literature points out the involvement of K(+) (ATP) channel, modulation of protein with anti-erectile effects, as well as involvement of the nitrergic pathway through a complex cross-talk. A new drug called H(2) S-donating sildenafil (ACS6), which incorporated an H(2) S-donating moiety in sildenafil, has been developed. While more studies are still needed, this heralded a new pharmacotherapeutical approach, which is multipronged in nature.
Given the mounting evidence of H(2) S's role in erectile function and how it appears to achieve its pro-erectile effects through different mechanisms, H(2) S represents a potentially important treatment alternative or adjunct to PDE5 inhibitors.
目前,治疗勃起功能障碍(ED)的药物治疗主要依赖于磷酸二酯酶 5(PDE5)抑制剂,但相当一部分 ED 患者对这种治疗方法有抗性,因此需要寻找替代治疗方法。我们回顾了现有的已发表数据,分析了目前关于硫化氢(H₂S)作为一种新型治疗药物的作用,及其在性功能方面的支持作用的证据。
讨论 H₂S 在勃起功能中的作用、其可能的作用机制,以及如何利用这些知识进行治疗。
通过 Pubmed 和 Medline 搜索,确定了原始文章和综述。
同行评审出版物的数据。
来自不同物种的动物研究,包括在人类中进行的体外研究,都证明了 H₂S 的促勃起作用。其作用机制尚不清楚,但文献中的证据表明,H₂S 涉及 K+(ATP)通道,调节具有抗勃起作用的蛋白,以及通过复杂的串扰涉及氮能途径。一种名为 H₂S 供体西地那非(ACS6)的新药已经被开发出来,它在西地那非中加入了 H₂S 供体部分。虽然还需要更多的研究,但这预示着一种新的多管齐下的药物治疗方法。
鉴于 H₂S 在勃起功能中的作用的越来越多的证据,以及它似乎通过不同的机制发挥其促勃起作用,H₂S 代表了一种潜在的重要的治疗选择或 PDE5 抑制剂的辅助治疗。