Francis Sharron H, Corbin Jackie D
Department of Molecular Physiology and Biophysics, Light Hall, Room 702, Vanderbilt University School of Medicine, Nashville, TN 37232-0615, USA.
Urol Clin North Am. 2005 Nov;32(4):419-29, vi. doi: 10.1016/j.ucl.2005.08.001.
This article discusses the role of phosphodiesterase-5 (PDE-5) inhibition in the molecular biology of erectile function and dysfunction. Commercially marketed PDE-5 inhibitors are highly specific for PDE-5, and in the face of continuing cyclic GMP (cGMP) synthesis,elevate cellular cGMP. This elevation results from direct competitive inhibition of PDE-5 and from blocking the negative feedback regulation of the enzyme. Elevation of cGMP activates cGMP-dependent protein kinase, which mediates the effects of the cGMP-signaling pathway to decrease smooth muscle tone and dilate penile vascular smooth muscle. By exploiting features of PDE-5 regulatory mechanisms that modulate PDE-5 function, the inhibitors enhance their own potencies.
本文讨论了磷酸二酯酶-5(PDE-5)抑制在勃起功能和功能障碍分子生物学中的作用。市售的PDE-5抑制剂对PDE-5具有高度特异性,在持续的环磷酸鸟苷(cGMP)合成的情况下,可提高细胞内cGMP水平。这种升高是由于对PDE-5的直接竞争性抑制以及阻断该酶的负反馈调节所致。cGMP的升高激活了cGMP依赖性蛋白激酶,该激酶介导cGMP信号通路的作用,以降低平滑肌张力并扩张阴茎血管平滑肌。通过利用调节PDE-5功能的PDE-5调节机制的特征,这些抑制剂增强了自身的效力。