Trends in Cardiovascular Medicine
Volume 18, Issue 1 , Pages 15-19, January 2008

Composition and Functions of Vascular Nicotinamide Adenine Dinucleotide Phosphate Oxidases

  • Ralf P. Brandes

      Affiliations

    • Corresponding Author InformationAddress correspondence to: Ralf P. Brandes, Institut für Kardiovaskuläre Physiologie, Johann Wolfgang Goethe-Universität, Theodor-Stern-Kai 7, D-60596 Frankfurt am Main, Germany. Tel.: (+49) 69 6301 6995; fax: (+49) 69 6301 7668.
  • ,
  • Katrin Schröder

Institut für Kardiovaskuläre Physiologie, Johann Wolfgang Goethe-Universität, D-60596 Frankfurt am Main, Germany.

Nicotinamide adenine dinucleotide phosphate (NADPH) oxidases are important sources of reactive oxygen species (ROS) and are expressed in at least three different homologues in the vasculature. The enzymes consist of a membrane complex of one of the large catalytically active Nox proteins and p22phox and different cytosolic subunits. Reactive oxygen species formation by the nicotinamide adenine dinucleotide phosphate oxidases Nox1 and Nox2 in arteries is a consequence of an activation of the enzymes by different stimuli such as growth factors, cytokines, and cardiovascular risk factors (cigarette smoke, high blood pressure, oxidized lipids). Nox4, in contrast, is constitutively active, and therefore, ROS formation by this enzyme is controlled on the expression level of the protein. The negative vascular effects of ROS, such as endothelial dysfunction, vascular hypertrophy, aneurysm formation, and inflammatory activation, appear to be the consequence of an activation of Nox1 and Nox2. Nox4, in contrast, potentially elicits positive effects because it promotes differentiation and reduces proliferation of cells. Consequently, selective pharmacologic inhibition of Nox proteins has a potential to interfere with cardiovascular disease initiation and progression.

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PII: S1050-1738(07)00242-3

doi:10.1016/j.tcm.2007.11.001

Trends in Cardiovascular Medicine
Volume 18, Issue 1 , Pages 15-19, January 2008