Literature DB >> 24281316

Pharmacologic therapy for erectile dysfunction and its interaction with the cardiovascular system.

Nikolaos Ioakeimidis1, John B Kostis.   

Abstract

Phosphodiesterase (PDE) enzymes are widely distributed throughout the body, having numerous effects and functions. The PDE type 5 (PDE5) inhibitors are widely used to treat erectile dysfunction (ED). Recent, intense preclinical and clinical research with PDE5 inhibitors has shed light on new mechanisms and has revealed a number of pleiotropic effects on the cardiovascular (CV) system. To date, PDE5 inhibition has been shown to be effective for the treatment of idiopathic pulmonary arterial hypertension, and both sildenafil and tadalafil are approved for this indication. However, current or future PDE5 inhibitors have the potential of becoming clinically useful in a variety of CV conditions such as heart failure, coronary artery disease, and hypertension. The present review discusses recent findings regarding pharmacologic treatment of ED and its interaction with the CV system and highlights current and future clinical applications beyond ED.

Entities:  

Keywords:  PDE5 inhibitors; cardiovascular disease; erectile dysfunction

Mesh:

Substances:

Year:  2013        PMID: 24281316     DOI: 10.1177/1074248413504034

Source DB:  PubMed          Journal:  J Cardiovasc Pharmacol Ther        ISSN: 1074-2484            Impact factor:   2.457


  6 in total

Review 1.  Chemical modulation of Kv7 potassium channels.

Authors:  Matteo Borgini; Pravat Mondal; Ruiting Liu; Peter Wipf
Journal:  RSC Med Chem       Date:  2021-01-14

2.  PDE5 inhibitors enhance the lethality of pemetrexed through inhibition of multiple chaperone proteins and via the actions of cyclic GMP and nitric oxide.

Authors:  Laurence Booth; Jane L Roberts; Andrew Poklepovic; Sarah Gordon; Paul Dent
Journal:  Oncotarget       Date:  2017-01-03

3.  PDE5 inhibitors enhance the lethality of [pemetrexed + sorafenib].

Authors:  Laurence Booth; Jane L Roberts; Andrew Poklepovic; Paul Dent
Journal:  Oncotarget       Date:  2017-02-21

4.  Use of the KlADH3 promoter for the quantitative production of the murine PDE5A isoforms in the yeast Kluyveromyces lactis.

Authors:  Silvia Cardarelli; Mauro Giorgi; Fabio Naro; Francesco Malatesta; Stefano Biagioni; Michele Saliola
Journal:  Microb Cell Fact       Date:  2017-09-22       Impact factor: 5.328

5.  Cellular Redox Metabolism Is Modulated by the Distinct Localization of Cyclic Nucleotide Phosphodiesterase 5A Isoforms.

Authors:  Silvia Cardarelli; Adriana Erica Miele; Federica Campolo; Mara Massimi; Patrizia Mancini; Stefano Biagioni; Fabio Naro; Mauro Giorgi; Michele Saliola
Journal:  Int J Mol Sci       Date:  2022-08-02       Impact factor: 6.208

6.  Molecular and functional characterization of Kv 7 channels in penile arteries and corpus cavernosum of healthy and metabolic syndrome rats.

Authors:  T A Jepps; S P Olesen; I A Greenwood; T Dalsgaard
Journal:  Br J Pharmacol       Date:  2016-02-26       Impact factor: 8.739

  6 in total

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