Literature DB >> 16297764

Nicotinamide adenine dinucleotide phosphate oxidase: a promiscuous therapeutic target for cardiovascular drugs?

Saima Muzaffar1, Nilima Shukla, Jamie Y Jeremy.   

Abstract

The increased expression and activity of the nicotinamide adenine dinucleotide phosphate (NADPH) oxidase complex has emerged as a major common factor in the etiology of all forms of cardiovascular diseases since the upregulation of intravascular NADPH oxidase results in the formation of superoxide (O(2)(-)), which in turn promotes vasculopathy. An ever-increasing number of drugs commonly used in cardiovascular medicine have been shown to influence NADPH oxidase expression and activity. These include nitric oxide donors, nitroaspirin, eicosanoids, phosphodiesterase inhibitors, corticosteroids, antioxidants, and specific inhibitors. The objective of this review is to discuss these drugs in relation to the mechanisms underlying their effects on NADPH oxidase activity and the expression and therapeutic implications of these effects.

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Year:  2005        PMID: 16297764     DOI: 10.1016/j.tcm.2005.09.001

Source DB:  PubMed          Journal:  Trends Cardiovasc Med        ISSN: 1050-1738            Impact factor:   6.677


  8 in total

1.  Acute inhibition of superoxide formation and Rac1 activation by nitric oxide and iloprost in human vascular smooth muscle cells in response to the thromboxane A2 analogue, U46619.

Authors:  S Muzaffar; N Shukla; M Bond; G Sala-Newby; G D Angelini; A C Newby; J Y Jeremy
Journal:  Prostaglandins Leukot Essent Fatty Acids       Date:  2008-04-16       Impact factor: 4.006

2.  Superoxide from NADPH oxidase upregulates type 5 phosphodiesterase in human vascular smooth muscle cells: inhibition with iloprost and NONOate.

Authors:  S Muzaffar; N Shukla; M Bond; G B Sala-Newby; A C Newby; G D Angelini; J Y Jeremy
Journal:  Br J Pharmacol       Date:  2008-07-28       Impact factor: 8.739

3.  Improvement of vascular function by acute and chronic treatment with the PDE-5 inhibitor sildenafil in experimental diabetes mellitus.

Authors:  A Schäfer; D Fraccarollo; S Pförtsch; U Flierl; C Vogt; J Pfrang; A Kobsar; T Renné; M Eigenthaler; G Ertl; J Bauersachs
Journal:  Br J Pharmacol       Date:  2007-09-24       Impact factor: 8.739

4.  Sildenafil citrate concentrations not affecting oxidative phosphorylation depress H2O2 generation by rat heart mitochondria.

Authors:  Maria A S Fernandes; Ricardo J F Marques; Joaquim A F Vicente; Maria S Santos; Pedro Monteiro; António J M Moreno; José B A Custódio
Journal:  Mol Cell Biochem       Date:  2007-11-16       Impact factor: 3.396

5.  H2S-donating sildenafil (ACS6) inhibits superoxide formation and gp91phox expression in arterial endothelial cells: role of protein kinases A and G.

Authors:  S Muzaffar; J Y Jeremy; A Sparatore; P Del Soldato; G D Angelini; N Shukla
Journal:  Br J Pharmacol       Date:  2008-09-01       Impact factor: 8.739

6.  Superoxide Mediates Depressive Effects Induced by Hydrogen Sulfide in Rostral Ventrolateral Medulla of Spontaneously Hypertensive Rats.

Authors:  Haiyun Yu; Haiyan Xu; Xiaoni Liu; Nana Zhang; Anqi He; Jerry Yu; Ning Lu
Journal:  Oxid Med Cell Longev       Date:  2015-05-11       Impact factor: 6.543

7.  Genotype-driven identification of a molecular network predictive of advanced coronary calcium in ClinSeq® and Framingham Heart Study cohorts.

Authors:  Cihan Oguz; Shurjo K Sen; Adam R Davis; Yi-Ping Fu; Christopher J O'Donnell; Gary H Gibbons
Journal:  BMC Syst Biol       Date:  2017-10-26

8.  Sildenafil Ameliorates Advanced Glycation End Products-Induced Mitochondrial Dysfunction in HT-22 Hippocampal Neuronal Cells.

Authors:  Soon Ki Sung; Jae Suk Woo; Young Ha Kim; Dong Wuk Son; Sang Weon Lee; Geun Sung Song
Journal:  J Korean Neurosurg Soc       Date:  2016-05-10
  8 in total

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