Literature DB >> 18855607

Classical inhibitors of NOX NAD(P)H oxidases are not specific.

Elisabetta Aldieri1, Chiara Riganti, Manuela Polimeni, Elena Gazzano, Cristina Lussiana, Ivana Campia, Dario Ghigo.   

Abstract

NAD(P)H oxidases (NOXs) are a family of enzymes catalyzing the univalent reduction of oxygen to produce the superoxide anion radical, which in turn can be converted in other reactive oxygen species (ROS) and may participate to the formation of reactive nitrogen derivatives, such as peroxynitrite. By virtue of their activity, NOXs may represent a double-edged sword for the organism's homeostasis. On one hand ROS participate in host defence by killing invading microbes and may regulate several important physiological functions, such as cell signalling, regulation of cell growth and differentiation, oxygen sensing, angiogenesis, fertilization and control of vascular tone. On the other hand ROS may play an important role in pathological processes such as hypertension, atherosclerosis, diabetes, cancer, ischemia/reperfusion injury, neurodegenerative diseases. Many roles suggested for NOXs in various tissues and physiopathological situations have been inferred by the in vitro and in vivo effects of several NOX inhibitors. In particular, most studies are based on the use of two compounds, diphenyleneiodonium and apocynin. Aim of this review is to describe the main features of these two compounds, to show that they cannot be used as specific NOX inhibitors and to solicit researchers to find other tools for investigating the role of NOXs.

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Year:  2008        PMID: 18855607     DOI: 10.2174/138920008786049285

Source DB:  PubMed          Journal:  Curr Drug Metab        ISSN: 1389-2002            Impact factor:   3.731


  83 in total

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Journal:  Plant Mol Biol       Date:  2010-09-05       Impact factor: 4.076

2.  Antiproliferative mechanisms of action of the flavin dehydrogenase inhibitors diphenylene iodonium and di-2-thienyliodonium based on molecular profiling of the NCI-60 human tumor cell panel.

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Review 3.  Targeting NOX enzymes in the central nervous system: therapeutic opportunities.

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Review 4.  NADPH oxidase- and mitochondria-derived reactive oxygen species in proinflammatory microglial activation: a bipartisan affair?

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Journal:  Antioxid Redox Signal       Date:  2013-04-20       Impact factor: 8.401

7.  Intermittent Hypoxia-Induced Parvalbumin-Immunoreactive Interneurons Loss and Neurobehavioral Impairment is Mediated by NADPH-Oxidase-2.

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8.  Nox2 and Cyclosporine-Induced Renal Hypoxia.

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Review 9.  Redox control of leukemia: from molecular mechanisms to therapeutic opportunities.

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Journal:  Antioxid Redox Signal       Date:  2012-09-28       Impact factor: 8.401

10.  Hypoxia-inducible factor-1 activation in nonhypoxic conditions: the essential role of mitochondrial-derived reactive oxygen species.

Authors:  David A Patten; Véronique N Lafleur; Geneviève A Robitaille; Denise A Chan; Amato J Giaccia; Darren E Richard
Journal:  Mol Biol Cell       Date:  2010-07-21       Impact factor: 4.138

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