Article

Novel Competitive Inhibitor of NAD(P)H Oxidase Assembly Attenuates Vascular O<sub>2</sub><sup>−</sup>and Systolic Blood Pressure in Mice

Federico E. ReyFrom the Hypertension and Vascular Research Division (F.E.R., M.E.C., A.K., P.J.P.), Henry Ford Hospital, Detroit, Mich; and Veterinary Molecular Biology Laboratory (M.T.Q.), Montana State University, Bozeman, MontEugenia Cifuentes-PaganoFrom the Hypertension and Vascular Research Division (F.E.R., M.E.C., A.K., P.J.P.), Henry Ford Hospital, Detroit, Mich; and Veterinary Molecular Biology Laboratory (M.T.Q.), Montana State University, Bozeman, MontArash KiarashFrom the Hypertension and Vascular Research Division (F.E.R., M.E.C., A.K., P.J.P.), Henry Ford Hospital, Detroit, Mich; and Veterinary Molecular Biology Laboratory (M.T.Q.), Montana State University, Bozeman, MontMark T. QuinnFrom the Hypertension and Vascular Research Division (F.E.R., M.E.C., A.K., P.J.P.), Henry Ford Hospital, Detroit, Mich; and Veterinary Molecular Biology Laboratory (M.T.Q.), Montana State University, Bozeman, MontPatrick J. PaganoFrom the Hypertension and Vascular Research Division (F.E.R., M.E.C., A.K., P.J.P.), Henry Ford Hospital, Detroit, Mich; and Veterinary Molecular Biology Laboratory (M.T.Q.), Montana State University, Bozeman, Mont

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Abstract

We previously reported enhanced expression of the p67(phox) and gp91(phox) components of NAD(P)H oxidase in angiotensin (Ang) II-induced hypertension, suggesting de novo assembly in response to Ang II. To examine the direct involvement of NAD(P)H oxidases in Ang II-induced O(2)(-) production, we designed a chimeric peptide that inhibits p47(phox) association with gp91(phox) in NAD(P)H oxidase (gp91ds-tat). This was achieved by linking a 9-amino acid peptide (aa) derived from HIV-coat protein (tat) to a 9-aa sequence of gp91(phox) (known to interact with p47(phox)). As a control, we constructed a chimera containing tat and a scrambled gp91 sequence (scramb-tat). We found that gp91ds-tat decreased O(2)(-) levels in aortic rings treated with Ang II (10 pmol/L) but had no effect on either the O(2)(-)-generating enzyme xanthine oxidase or potassium superoxide-generated O(2)(-). We infused vehicle, Ang II (0.75 mg. kg(-1). d(-1)), Ang II+gp91ds-tat (10 mg. kg(-1). d(-1)), or Ang II+scramb-tat intraperitoneally in C57Bl/6 mice and measured systolic blood pressure (SBP) on days 0, 3, 5, and 7 of infusion. SBP increased by day 3 in mice given Ang II and Ang II+scramb-tat but was significantly lower with Ang II+gp91-tat. On day 7, SBP was still significantly inhibited in mice given Ang II+gp91ds-tat, whereas Ang II-induced O(2)(-) production was inhibited throughout the aorta as detected by dihydroethidium staining, consistent with the ability of this inhibitor to block the various vascular NAD(P)H oxidase isoforms. These data support the hypothesis that inhibition of the interaction of p47(phox) and gp91(phox) (or its homologues) can block O(2)(-) production and attenuate blood pressure elevation in mice.

Identifiers

DOI: 10.1161/hh1701.096037

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