磷酸二酯酶-5 (PDE5)抑制剂治疗勃起功能障碍的研究进展

Mayur S. Jain, Shailesh K. Koradia
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引用次数: 1

摘要

磷酸二酯酶5型抑制剂(PDE5抑制剂)是一种血管舒张药物,其作用是阻断cgmp特异性磷酸二酯酶5 (PDE5)对供应各种组织的血管内壁平滑肌细胞中环状GMP的降解作用。这些药物扩张阴茎海绵体,通过性刺激促进勃起,并用于治疗勃起功能障碍(ED)。西地那非是第一个有效的ED口服治疗药物。由于PDE5也存在于肺内小动脉壁的平滑肌中,两种PDE5抑制剂西地那非和他达拉非被fda批准用于治疗肺动脉高压。截至2019年,PDE5抑制剂更广泛的心血管益处正在受到重视。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Phosphodiesterase-5 (PDE5) Inhibitors in the Treatment of Erectile Dysfunction: A Review
A phosphodiesterase type 5 inhibitor (PDE5 inhibitor) is a vasodilating drug which works by blocking the degradative action of cGMP-specific phosphodiesterase type 5 (PDE5) on cyclic GMP in the smooth muscle cells lining the blood vessels supplying various tissues. These drugs dilate the corpora cavernosa of the penis, facilitating erection with sexual stimulation, and are used in the treatment of erectile dysfunction (ED). Sildenafil was the first effective oral treatment available for ED. Because PDE5 is also present in the smooth muscle of the walls of the arterioles within the lungs, two PDE5 inhibitors, sildenafil and tadalafil, are FDA-approved for the treatment of pulmonary hypertension. As of 2019, the wider cardiovascular benefits of PDE5 inhibitors are being appreciated.
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