Phosphodiesterase type 5 inhibitors (PDE5) application in treatment of erectile dysfunction in general practice Review article

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Krzysztof Dęmbe
Przemysław Krasnodębski
Mariusz Jasik
Anna Skowrońska
Piotr Nehring

Abstract

Erectile dysfunction (ED) defined as inability to produce or maintain an erection for sexual intercourse affects over 150 millions men. This number is expected to increase to more than 300 millions men by 2025. ED has been associated with the cardiovascular risk factors and has been proposed to be a coronary artery disease risk equivalent. Oral treatment for erectile dysfunction with type 5 phosphodiesterase enzyme (PDE5) inhibitors was introduced in 1998 and has been considered the first line of treatment for ED. PDE5 inhibitors increase cGMP levels in smooth-muscle cells, cGMP is a second messenger for the vasodilator effects of nitric oxide. Inhibition of PDE5 reduces enzymatic degradation of cGMP, resulting increases in blood flow into cavernous sinus. Three PDE5 inhibitors: sildenafil citrate, vardenafil and tadalafil are approved for the treatment of ED. Data from studies suggest that the available PDE5 inhibitor therapies are effective and safe in treating men with ED.

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How to Cite
Dęmbe , K., Krasnodębski , P., Jasik , M., Skowrońska , A., & Nehring , P. (2013). Phosphodiesterase type 5 inhibitors (PDE5) application in treatment of erectile dysfunction in general practice. Cardiology in Practice, 7(4), 27-33. Retrieved from https://journalsmededu.pl/index.php/kwp/article/view/1552
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