Pressure overload-induced myocardial hypertrophy in mice does not require gp91phox

Circulation. 2004 Mar 9;109(9):1168-71. doi: 10.1161/01.CIR.0000117229.60628.2F. Epub 2004 Feb 23.

Abstract

Background: Reactive oxygen species (ROS) may mediate pressure overload-induced myocardial hypertrophy. NADPH oxidase may be involved in this process, because its expression and activity are upregulated by pressure overload and because myocardial hypertrophy caused by a subpressor infusion of angiotensin is attenuated in mice deficient in the gp91phox catalytic subunit of NADPH oxidase.

Methods and results: To test the role of NADPH oxidase-dependent ROS in mediating pressure overload-induced myocardial hypertrophy, we subjected transgenic mice lacking gp91phox to chronic pressure overload caused by constriction of the ascending aorta. Contrary to our hypothesis, neither myocardial hypertrophy nor NADPH-dependent superoxide generation was decreased in gp91phox-deficient mice after aortic constriction. Aortic constriction caused an exaggerated increase in p22phox and p47phox mRNA in gp91phox-deficient mice.

Conclusions: These results indicate that gp91phox is not necessary for pressure overload-induced hypertrophy in the mouse and suggest the involvement of another source of ROS, possibly an NADPH oxidase that does not require the gp91phox subunit.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Aorta
  • Cardiomegaly / diagnosis
  • Cardiomegaly / enzymology*
  • Cardiomegaly / etiology
  • Constriction
  • Glutathione / metabolism
  • Mice
  • Mice, Inbred C57BL
  • Mice, Transgenic
  • NADPH Oxidases / genetics
  • NADPH Oxidases / physiology*
  • Pressure
  • Protein Subunits / genetics
  • Protein Subunits / physiology
  • RNA, Messenger / metabolism

Substances

  • Protein Subunits
  • RNA, Messenger
  • NADPH Oxidases
  • Glutathione