Acute ethanol intake induces superoxide anion generation and mitogen-activated protein kinase phosphorylation in rat aorta: A role for angiotensin type 1 receptor


Autoria(s): Yogi, Alvaro; Callera, Gláucia Elena; Mecawi, Andre S.; Batalhão, Marcelo Eduardo; Carnio, Evelin Capellari; Rodrigues, Jose Antunes; Queiroz, Regina Helena Costa; Touyz, Rhian M.; Tirapelli, Carlos Renato
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

31/10/2013

31/10/2013

02/08/2013

Resumo

Ethanol intake is associated with increase in blood pressure, through unknown mechanisms. We hypothesized that acute ethanol intake enhances vascular oxidative stress and induces vascular dysfunction through renin-angiotensin system (RAS) activation. Ethanol (1 g/kg; p.o. gavage) effects were assessed within 30 min in male Wistar rats. The transient decrease in blood pressure induced by ethanol was not affected by the previous administration of losartan (10 mg/kg; p.o. gavage), a selective ATI receptor antagonist. Acute ethanol intake increased plasma renin activity (PRA), angiotensin converting enzyme (ACE) activity, plasma angiotensin I (ANG I) and angiotensin II (ANG II) levels. Ethanol induced systemic and vascular oxidative stress, evidenced by increased plasma thiobarbituric acid-reacting substances (TBARS) levels, NAD(P) H oxidase-mediated vascular generation of superoxide anion and p47phox translocation (cytosol to membrane). These effects were prevented by losartan. Isolated aortas from ethanol-treated rats displayed increased p38MAPK and SAPK/JNK phosphorylation. Losartan inhibited ethanol-induced increase in the phosphorylation of these kinases. Ethanol intake decreased acetylcholine-induced relaxation and increased phenylephrine-induced contraction in endothelium-intact aortas. Ethanol significantly decreased plasma and aortic nitrate levels. These changes in vascular reactivity and in the end product of endogenous nitric oxide metabolism were not affected by losartan. Our study provides novel evidence that acute ethanol intake stimulates RAS activity and induces vascular oxidative stress and redox-signaling activation through AT(1)-dependent mechanisms. These findings highlight the importance of RAS in acute ethanol-induced oxidative damage. (c) 2012 Elsevier Inc. All rights reserved.

Canadian Institutes of Health Research

Canadian Institutes of Health Research

Conselho Nacional de Desenvolvimento Cientifico e Tecnologico

Conselho Nacional de Desenvolvimento Cientifico e Tecnologico [470556/2010-2]

Fundacao de Amparo a Pesquisa do Estado de Sao Paulo [2010/05815-4]

Fundacao de Amparo a Pesquisa do Estado de Sao Paulo

Identificador

TOXICOLOGY AND APPLIED PHARMACOLOGY, SAN DIEGO, v. 264, n. 3, supl. 1, Part 3, pp. 470-478, 37196, 2012

0041-008X

http://www.producao.usp.br/handle/BDPI/37095

10.1016/j.taap.2012.08.029

http://dx.doi.org/10.1016/j.taap.2012.08.029

Idioma(s)

eng

Publicador

ACADEMIC PRESS INC ELSEVIER SCIENCE

SAN DIEGO

Relação

TOXICOLOGY AND APPLIED PHARMACOLOGY

Direitos

closedAccess

Copyright ACADEMIC PRESS INC ELSEVIER SCIENCE

Palavras-Chave #ETHANOL #AORTA #SUPEROXIDE ANION #BLOOD PRESSURE #ANGIOTENSIN II #LOSARTAN #SMOOTH-MUSCLE-CELLS #INDUCED OXIDATIVE STRESS #NITRIC-OXIDE #SIGNAL-TRANSDUCTION #ALCOHOL-CONSUMPTION #ENDOTHELIAL INJURY #AT(2) RECEPTOR #HEART-RATE #HYPERTENSION #MECHANISMS #PHARMACOLOGY & PHARMACY #TOXICOLOGY
Tipo

article

original article

publishedVersion