gp91phox-containing NAD(P)H oxidase mediates attenuation of nitric oxide-dependent control of myocardial oxygen consumption by ANG II

Am J Physiol Heart Circ Physiol. 2005 Aug;289(2):H862-7. doi: 10.1152/ajpheart.00076.2005. Epub 2005 Mar 18.

Abstract

We have previously reported that ANG II stimulation increased superoxide anion (O2-) through the activation of NAD(P)H oxidase and inhibited nitric oxide (NO)-dependent control of myocardial oxygen consumption (MVo2) by scavenging NO. Our objective was to investigate the role of NAD(P)H oxidase, especially the gp91phox subunit, in the NO-dependent control of MVo2. MVo2 in mice with defects in the expression of gp91phox [gp91(phox)(-/-)] was measured with a Clark-type oxygen electrode. Baseline MVo2 was not significantly different between wild-type (WT) and gp91(phox)(-/-) mice. Stimulation of NO production by bradykinin (BK) induced significant decreases in MVo2 in WT mice. BK-induced reduction in MVo2 was enhanced in gp91(phox)(-/-) mice. BK-induced reduction in MVo2 in WT mice was attenuated by 10(-8) mol/l ANG II, which was restored by coincubation with Tiron or apocynin. In contrast to WT mice, BK-induced reduction in MVo2 in gp91(phox)(-/-) mice was not altered by ANG II. There was a decrease in lucigenin (5 x 10(-6) mol/l)-detectable O2- in gp91(phox)(-/-) mice compared with WT mice. ANG II resulted in significant increases in O2- production in WT mice, which was inhibited by coincubation with Tiron or apocynin. However, ANG II had no effect on O2- production in gp91(phox)(-/-) mice. Histological examination showed that the development of abscesses and/or the invasion of inflammatory cells occurred in lungs and livers but not in hearts and kidneys from gp91(phox)(-/-) mice. These results indicate that the gp91(phox) subunit of NAD(P)H oxidase mediates O2- production through the activation of NAD(P)H oxidase and attenuation of NO-dependent control of MVo2 by ANG II.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Abscess / etiology
  • Abscess / pathology
  • Angiotensin II / pharmacology*
  • Animals
  • Bradykinin / pharmacology
  • Liver Diseases / etiology
  • Liver Diseases / pathology
  • Lung Abscess / etiology
  • Lung Abscess / pathology
  • Membrane Glycoproteins / deficiency
  • Membrane Glycoproteins / metabolism*
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Myocardium / metabolism*
  • NADPH Oxidase 2
  • NADPH Oxidases / deficiency
  • NADPH Oxidases / metabolism*
  • Nitric Oxide / metabolism*
  • Oxygen Consumption / drug effects*
  • Papillary Muscles / metabolism
  • Superoxides / metabolism

Substances

  • Membrane Glycoproteins
  • Superoxides
  • Angiotensin II
  • Nitric Oxide
  • Cybb protein, mouse
  • NADPH Oxidase 2
  • NADPH Oxidases
  • Bradykinin