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January 6, 2009 |
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Part of the physiological process of erection involves the release of nitric oxide (NO) in vasculature of the corpus cavernosum. NO activates the enzyme guanylate cyclase which results in increased levels of cyclic guanosine monophosphate (cGMP), leading to smooth muscle relaxation in blood vessels supplying the corpus cavernosum, resulting in increased inflow of blood and an erection. PDE5 inhibitors inhibit the degradation of cGMP by phosphodiesterase type 5 (PDE5), increasing bloodflow to the penis during sexual stimulation. This mode of action means that PDE5 inhibitors are ineffective without sexual stimulation. Indications PDE5 inhibitors are clinically indicated for the treatment of erectile dysfunction. Sildenafil, the prototypical PDE5 inhibitor, was originally discovered during the search of a novel treatment for angina. Recent studies are exploring its use as a treatment for pulmonary hypertension. (Kanthapillai, Lasserson & Walters, 2004) Contraindications PDE5 inhibitors are contraindicated in those taking nitrate medication. They are also contraindicated in men for whom sexual intercourse is inadvisable due to cardiovascular risk factors. (Rossi, 2004) Adverse drug reactions The occurrence of adverse drug reactions (ADRs) with PDE5 inhibitors appears to be dose related. Headache is a very common ADR, occurring in >10% of patients. Other common ADRs include: dizziness, flushing, dyspepsia, nasal congestion or rhinitis. (Rossi, 2004) Other ADRs and their incidence vary with the agent and are listed in their individual pages. Sildenafil was the prototypical member of the PDE5 inhibitors. Two other agents, with their own advantages/disadvantages are also available.
Category: PDE5 inhibitors|* This article is licensed under the GNU Free Documentation License. It uses material from the Wikipedia article "PDE5 inhibitor".
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