PDE5 Inhibitors: In Vitro and In Vivo Pharmacological Profile

被引:61
作者
Kouvelas, D. [1 ]
Goulas, A. [1 ]
Papazisis, G. [1 ]
Sardeli, C. [1 ]
Pourzitaki, C. [1 ]
机构
[1] Aristotle Univ Thessaloniki, Dept Pharmacol, Sch Med, GR-54006 Thessaloniki, Greece
关键词
PDE5; inhibitors; sildenafil; vardenafil; tadafil; PULMONARY ARTERIAL-HYPERTENSION; TRANSIENT GLOBAL AMNESIA; PHOSPHODIESTERASE TYPE 5; NITRIC-OXIDE SYNTHASE; CYCLIC-GMP PHOSPHODIESTERASE; SILDENAFIL CITRATE THERAPY; DEPENDENT PROTEIN-KINASE; URETERAL SMOOTH-MUSCLE; CEREBRAL-BLOOD-FLOW; ERECTILE DYSFUNCTION;
D O I
10.2174/138161209789206971
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
PDE5 inhibitors have been clearly established as first-line therapy for the treatment of erectile dysfunction (ED). Three PDE5 inhibitors - sildenafil (Viagra (R)), vardenafil (Levitra (R)) and tadalafil (Cialis (R)) - are currently approved by the FDA and the EMEA for use in ED, whereas sildenafil is also marketed under a different proprietary name (Revatio (R)) for the treatment of pulmonary arterial hypertension (PAH). A forth PDE5 inhibitor, udenafil (Zydena (R)) is currently marketed. In the present review the molecular basis and the mechanism of action of PDE5 inhibitors is discussed. In addition experimental and clinical data concerning their effects on different tissues, organs and systems is systematically reviewed and their possible beneficial action in numerous disorders is presented.
引用
收藏
页码:3464 / 3475
页数:12
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