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Nonurologic applications of phosphodiesterase type 5 inhibitors

Current Sexual Health Reports, 2007
Phosphodiesterase type 5 (PDE5) is an enzyme that catalyzes hydrolytic degradation of cyclic guanosine monophosphate, an essential intracellular second messenger that modulates diverse biologic processes in living cells. Three selective inhibitors of PDE5, sildenafil, vardenafil, and tadalafil, have been successfully used by millions of people ...
Rakesh C. Kukreja   +2 more
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Type 5 Phosphodiesterase Inhibitors: Curing Erectile Dysfunction

European Urology, 2006
Basic science research on erectile physiology has focused on the pathogenesis of erectile dysfunction (ED) and has provided convincing evidence that ED is predominately a disease of vascular etiology correlating with coronary artery disease, hypertension, atherosclerosis, hyperlipidemia, smoking, and diabetes mellitus [1,2].
Wayne J.G. Hellstrom, Muammer Kendirci
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Phosphodiesterase type 5 inhibitors and endothelial function

Current Sexual Health Reports, 2007
Erectile dysfunction (ED) and endothelial dysfunction are common in individuals with multiple cardiovascular risk factors (CRFs) and are longitudinal predictors of cardiovascular events. ED is associated with systemic endothelial cell activation/dysfunction independent from CRFs or from diffuse, unrecognized vascular damage.
Antonio Aversa, Roberto Bruzziches
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Phosphodiesterase Type 5 Inhibitors: Molecular Pharmacology and Interactions with other Phosphodiesterases

Current Pharmaceutical Design, 2005
Erectile function is determined by tight regulation of relaxation or contraction of corpus cavernosal smooth muscle, which is the result of a long and complex chain of molecular events. Control of erectile function resides in signaling pathways of the central and peripheral nervous system, as well as intracellular events in the penile smooth muscle ...
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FR226807: a potent and selective phosphodiesterase type 5 inhibitor

European Journal of Pharmacology, 2001
We describe the pharmacological characteristics of a novel phosphodiesterase type 5 inhibitor FR226807, N-(3,4-dimethoxybenzyl)-2-[[(1R)-2-hydroxy-1-methylethyl]amino]-5-nitrobenzamide. FR226807 inhibited phosphodiesterase type 5 isolated from human platelets with an IC(50) value of 1.1 nM. FR226807 also inhibited phosphodiesterase type 6 with an IC(50)
N, Hosogai   +12 more
openaire   +2 more sources

Chronic dosing of phosphodiesterase type 5 inhibitors

Current Sexual Health Reports, 2008
Ten years ago, the introduction of sildenafil citrate for the treatment of erectile dysfunction fundamentally changed the field of sexual medicine. The sexual indications, along with the pharmacologic characteristics of this drug, led to its approval for on-demand use.
openaire   +1 more source

Effects of phosphodiesterase type 5 inhibitors on Raynaud’s phenomenon

Rheumatology International, 2014
Raynaud's phenomenon (RP) is commonly observed in fingers and toes of patients with connective tissue diseases (CTDs). However, existing vasodilators have very limited efficacy. In this study, phosphodiesterase type 5 inhibitors (PDE-5Is) were administered to evaluate efficacy on RP.
Yasuyuki, Kamata, Seiji, Minota
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Thromboangiitis obliterans successfully treated with phosphodiesterase type 5 inhibitors

Vascular, 2013
Thromboangiitis obliterans, or Buerger’s disease, is a non-atherosclerotic, segmental, inflammatory disease affecting the small- and medium-sized vessels of the distal extremities. Other than discontinuation of tobacco, there is no standard-of-care treatment.
Aryeh M, Abeles   +3 more
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Optimizing response to phosphodiesterase type 5 inhibitors

Current Sexual Health Reports, 2007
Although using phosphodiesterase type 5 inhibitors to treat erectile dysfunction has been highly effective in clinical trials, many men do not achieve their desired goals and stop using the medication after a few attempts. The notion of optimizing response to pharmacologic interventions is relatively new to clinicians.
openaire   +1 more source

[Erectile dysfunction and phosphodiesterase type 5 inhibitors].

Revue medicale de Bruxelles, 2003
Erectile dysfunction affects 150 millions of men and its prevalence increases with age. The improvement of life expectancy will increase the worldwide prevalence to 300 million in 2025. Oral treatments are nowadays the first line therapy for the vast majority of people as they have a good reliability and tolerance and restore more spontaneity.
T, Roumeguère   +2 more
openaire   +1 more source

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