Results 201 to 210 of about 177,264 (261)
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Phosphodiesterase type 5 inhibitors in pulmonary arterial hypertension

Advances in Therapy, 2009
Pulmonary arterial hypertension (PAH) is a rare disease characterized by vascular proliferation and remodeling, resulting in a progressive increase in pulmonary arterial resistance, right heart failure, and death. The pathogenesis of PAH is multifactorial, with endothelial cell dysfunction playing an integral role.
David, Montani   +8 more
openaire   +2 more sources

Phosphodiesterase Type 5 Inhibitor Abuse: A Critical Review

Current Drug Abuse Reviewse, 2011
Abuse of sildenafil has been reported since its introduction in 1999 and commonly documented in combination with illicit drugs among men and women of all ages. Increased risks of sexually transmissible diseases including HIV have been associated with sildenafil use in men who have sex with men.
Gregory, Lowe, Raymond, Costabile
openaire   +2 more sources

Therapeutic potential of phosphodiesterase type 5 inhibitors in heart failure with preserved ejection fraction and combined post- and pre-capillary pulmonary hypertension.

International Journal of Cardiology, 2019
OBJECTIVE Heart failure with preserved ejection fraction (HFpEF) is frequently associated with pulmonary hypertension (PH), which substantially impacts survival.
T. Kramer   +7 more
semanticscholar   +1 more source

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
openaire   +1 more source

Cardiovascular Safety of Phosphodiesterase Type 5 Inhibitors After Nearly 2 Decades on the Market.

Sexual Medicine Reviews, 2018
BACKGROUND The phosphodiesterase-5 (PDE5) inhibitors that have been available for nearly 20 years are highly effective in treating erectile dysfunction and have been consistently shown to be safe when used according to package insert instructions.
R. Kloner   +4 more
semanticscholar   +1 more source

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
openaire   +1 more source

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
openaire   +1 more source

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 ...
openaire   +2 more sources

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

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