Gonzalez-Cadavid N F, Rajfer J
Division of Urology, Harbor-UCLA Medical Center, Torrance, CA, USA.
Department of Surgery, Los Angeles Biomedical Research Institute, Torrance, CA, USA.
Int J Impot Res. 2019 Mar;31(2):57-60. doi: 10.1038/s41443-018-0076-9. Epub 2018 Sep 26.
The FDA approval of Viagra (sildenafil) for the on demand treatment of erectile dysfunction (ED) through relaxation of the corporal and cavernosal vascular smooth muscle that results in an increase in blood flow to the corporal tissues stemmed from 2 decades of research, mainly at academic centers. This culminated in the finding of the nitric oxide/cGMP pathway as the mediator of penile erection, followed by some years of basic studies and clinical validation at Pfizer. Further on, new translational laboratory and animal research from our group initiated a second phase when we proposed an alternative therapeutic schedule and mechanism of action for PDE5 inhibitors (PDE5i) in both corporal veno-occlusive dysfunction (CVOD) and Peyronie's disease (PD), specifically, continuous long-term administration (CLTA) to achieve sustained levels of cGMP within the penis. Due to the extended half-life of the long-acting PDE5i, tadalafil, this new alternative encompasses preferentially daily administration, although shorter half-life PDE5i, like sildenafil and vardenafil work too, depending on the duration, dose, and frequency of their administration This novel use was initially supported by showing the antifibrotic/antioxidant effects of nitric oxide and cGMP, produced by the induction of iNOS, as a mechanism of defense against collagen deposition in the localized fibrotic plaque of PD in an avascular tissue, the tunica albuginea. Our studies on iNOS and the progressive diffuse fibrosis occurring in the smooth muscle in CVOD, led to proposing the CLTA of PDE5i for maintaining sustained cGMP levels both in PD and in CVOD in order to halt or regress the penile fibrosis. In CVOD, we showed that PDE5i protect the corporal smooth muscle and reduce myofibroblast activation and number, counteracting the underlying corporal tissue pathology that causes CVOD, and potentially ameliorating long-term CVOD or even curing it. This review is focused on this novel PDE5i anti-fibrotic therapeutic concept.
美国食品药品监督管理局(FDA)批准伟哥(西地那非)按需治疗勃起功能障碍(ED),其作用机制是通过使阴茎海绵体血管平滑肌松弛,增加阴茎海绵体组织的血流量,这一成果源于20年的研究,主要是在学术中心进行的。这最终促成了一氧化氮/cGMP途径作为阴茎勃起介质的发现,随后辉瑞公司进行了数年的基础研究和临床验证。此外,我们团队开展的新的转化实验室和动物研究开启了第二阶段,我们提出了一种针对阴茎静脉闭塞功能障碍(CVOD)和佩罗尼氏病(PD)的PDE5抑制剂(PDE5i)的替代治疗方案和作用机制,具体而言,即持续长期给药(CLTA)以在阴茎内实现cGMP的持续水平。由于长效PDE5i他达拉非的半衰期延长,这种新的替代方案优先考虑每日给药,不过半衰期较短的PDE5i,如西地那非和伐地那非,根据给药持续时间、剂量和频率也同样有效。这一新颖的用途最初得到了如下研究结果的支持:诱导诱导型一氧化氮合酶(iNOS)产生的一氧化氮和cGMP具有抗纤维化/抗氧化作用,这是在无血管组织白膜中局部纤维化斑块中抵御胶原蛋白沉积的一种防御机制。我们对iNOS以及CVOD平滑肌中发生的进行性弥漫性纤维化的研究,促使我们提出对PDE5i进行CLTA,以在PD和CVOD中维持cGMP的持续水平,从而阻止或逆转阴茎纤维化。在CVOD中,我们表明PDE5i可保护阴茎海绵体平滑肌,减少肌成纤维细胞的激活和数量,对抗导致CVOD的潜在阴茎海绵体组织病理变化,并有可能改善长期CVOD甚至治愈它。本综述聚焦于这一新颖的PDE5i抗纤维化治疗理念。