Hypertension caused by transgenic overexpression of Rac1

Antioxid Redox Signal. 2007 Jan;9(1):91-100. doi: 10.1089/ars.2007.9.91.

Abstract

Reactive oxygen species, including superoxide, are important mediators of the pathophysiology of hypertension. In the vasculature, superoxide antagonizes nitric oxide (NO*), resulting in increased vascular tone. The GTP binding protein Rac regulates a wide variety of cellular functions, including the activation of NADPH oxidase, the major source of O2*-in the blood vessel wall. An hypothesis is that Rac1 may act as an important regulator of vascular O2*- production, contributing to the balance between O2*- and NO* and maintaining consequent homeostasis of blood pressure. To alter the activity of vascular NADPH oxidase, the authors developed a transgenic animal model that overexpresses the human cDNA of the constitutively active mutant of Rac1 (RacCA) in smooth muscle cells using the smooth muscle +/--actin promoter. The RacCA transgenic had excessive amounts of O2*- in the vessel wall that, which led to heightened production of peroxynitrite, as detected by increased protein nitration and reduced NO* levels. RacCA mice developed moderate hypertension, which was corrected by N-acetyl-L-cysteine (NAC). RacCA transgenic mice also developed left ventricular hypertrophy as a secondary effect of pressure overload. The data suggest that Rac1 is a critical regulator of the redox state of blood vessels and homeostasis of blood pressure.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Actins / genetics
  • Animals
  • Antioxidants / metabolism
  • Aorta / metabolism
  • Blood Pressure / genetics
  • Female
  • Hypertension / etiology*
  • Hypertrophy, Left Ventricular / genetics
  • Mice
  • Mice, Transgenic
  • Myocytes, Smooth Muscle / metabolism*
  • Nitric Oxide / metabolism
  • Promoter Regions, Genetic
  • Proteins / metabolism
  • Reactive Oxygen Species / metabolism
  • Renin / metabolism
  • Tissue Distribution
  • Transgenes*
  • rac1 GTP-Binding Protein / genetics
  • rac1 GTP-Binding Protein / metabolism*

Substances

  • Actins
  • Antioxidants
  • Proteins
  • Reactive Oxygen Species
  • Nitric Oxide
  • Renin
  • rac1 GTP-Binding Protein