Department of Urology, Albert Einstein College of Medicine, Bronx, NY, USA.
Maturitas. 2012 Jan;71(1):20-7. doi: 10.1016/j.maturitas.2011.11.004. Epub 2011 Dec 7.
Erectile dysfunction (ED) is a neurovascular phenomenon modulated by hormonal, local biochemical, and biomechanical/structural factors of the penis. The success of the orally active phosphodiesterase inhibitors for the treatment of ED has boosted research activities into the physiology of the erectile mechanism. Peripheral intracellular signal transduction in the penis as well as central brain and spinal cord pathways controlling penile erection have been investigated and are now better understood. The results of this ongoing research have provided the basis for the development and introduction of several novel therapeutic modalities into the management of ED. Many novel pharmacotherapeutic approaches under development including the use of melanocortins and Rho-kinase inhibitors as well as the introduction of gene therapy and tissue engineering have demonstrated efficacy in animal as well as early human trials. This review describes the major new and evolving pharmacological advances in the field of oral pharmacotherapy for the treatment of male ED.
勃起功能障碍(ED)是一种由阴茎的激素、局部生化和生物力学/结构因素调节的神经血管现象。口服磷酸二酯酶抑制剂治疗 ED 的成功,促进了对勃起机制生理学的研究。目前已经对阴茎的外周细胞内信号转导以及控制阴茎勃起的中枢大脑和脊髓通路进行了研究,并对此有了更好的理解。这项正在进行的研究结果为开发和引入几种新的治疗方法来治疗 ED 提供了基础。许多正在开发中的新型药物治疗方法,包括使用黑素皮质素和 Rho 激酶抑制剂,以及引入基因治疗和组织工程,在动物和早期人体试验中都显示出了疗效。这篇综述描述了男性 ED 口服药物治疗领域的主要新的和不断发展的药理学进展。