Results 1 to 10 of about 79,696 (205)

Repurposing Phosphodiesterase-5 inhibitors as chemoadjuvants [PDF]

open access: yesFrontiers in Pharmacology, 2013
Phosphodiesterase-5 (PDE5) inhibitors have shown a beneficial effect in a variety of clinical conditions, such as benign prostate hyperplasia, pulmonary arterial hypertension, female sexual arousal disorder, overactive bladder, and incontinence, Raynaud's disease, heart failure and stroke among others (Sandner et al., 2007).
Amit K. Tiwari, Zhe-Sheng eChen
doaj   +3 more sources

Membrane-Mediated Action of Phosphodiesterase 5 Inhibitors [PDF]

open access: yesPharmaceutics
Background/Objectives: Phosphodiesterase 5 (PDE5) inhibitors, sildenafil, vardenafil, and tadalafil, activate the cyclic guanosine monophosphate pathway resulting in vascular smooth muscle relaxation.
Anna I. Malykhina   +2 more
doaj   +2 more sources

Advancements in Phosphodiesterase 5 Inhibitors: Unveiling Present and Future Perspectives [PDF]

open access: yesPharmaceuticals, 2023
Phosphodiesterase 5 (PDE5) inhibitors presented themselves as important players in the nitric oxide/cGMP pathway, thus exerting a profound impact on various physiological and pathological processes.
Ahmed K. ElHady   +3 more
doaj   +2 more sources

Phosphodiesterase-5 inhibitors: Raynaud's and beyond

open access: yesIndian Journal of Rheumatology, 2017
Phosphodiesterases (PDE) are a group of ubiquitously present enzymes involved in regulation of various cellular pathways. PDE5 acts to metabolize cyclic guanosine monophosphate (GMP).
Sanat Phatak   +3 more
doaj   +3 more sources

Phosphodiesterase Type 5 Inhibitors, Sport and Doping [PDF]

open access: yesCurrent Sports Medicine Reports, 2017
Phosphodiesterase type 5 inhibitors (PDE5i) (e.g., sildenafil, tadalafil, vardenafil, and avanafil) are drugs commonly used to treat erectile dysfunction, pulmonary arterial hypertension, and benign prostatic hyperplasia.
Borrione, Paolo   +8 more
core   +5 more sources

Phosphodiesterase-5 inhibitors for erectile function rehabilitation in patients undergoing nerve sparing radical prostatectomy: a scoping review [PDF]

open access: yesRevista do Colégio Brasileiro de Cirurgiões
Introduction: The aim of this study was to conduct a scoping review on the efficacy of phosphodiesterase-5 inhibitors (PDE-5Is) in rehabilitating erectile function in patients undergoing cavernous nerve sparing radical prostatectomy (NSRP).
GABRIEL CARVALHO ANDRADE GADELHA   +1 more
doaj   +2 more sources

Identifying Phosphodiesterase‐5 Inhibitors with Drug Repurposing Approach: Implications in Vasodysfunctional Disorders [PDF]

open access: yesChemistryOpen
Phosphodiesterase type 5 (PDE5) is a multidomain protein that plays a crucial role in regulating cellular cyclic guanosine monophosphate (cGMP), a key signaling molecule involved in various physiological processes.
Mohd Shahnawaz Khan   +5 more
doaj   +2 more sources

Determination of Phosphodiesterase Type-5 Inhibitors (PDE-5) in Dietary Supplements

open access: yesMolecules, 2023
This study proposed a high-performance thin-layer chromatography (HPTLC) screening method to detect phosphodiesterase 5 (PDE-5) inhibitors as possible adulterant agents in various dietary supplements.
Oana Ramona Cătălina Gheorghiu   +7 more
doaj   +1 more source

Mirodenafil Prevents Bladder Dysfunction Induced by Chronic Bladder Ischemia in Rats [PDF]

open access: yesInternational Neurourology Journal, 2015
Purpose: To investigate the protective effect of mirodenafil on bladder function in a rat model of chronic bladder ischemia (CBI). Methods: Twenty-four Sprague-Dawley rats were randomized to three groups: untreated, sham-operated rats (control group ...
Hoon Choi   +5 more
doaj   +1 more source

A review of phosphodiesterase type 5 inhibitors

open access: yesSouth African Family Practice, 2014
Currently, three phosphodiesterase type 5 (PDE5) inhibitors are available for clinical use in South Africa; sildenafil, vardenafil and tadalafil. The PDE inhibitors are used in males to treat erectile dysfunction.
N. Schellack, A. Agoro
doaj   +1 more source

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