Ethanol induces vascular relaxation via redox-sensitive and nitric oxide-dependent pathways


Autoria(s): Rocha, Juliana T.; Hipolito, Ulisses V.; Callera, Glaucia E.; Yogi, Alvaro; Anjos Neto Filho, Mario dos; Bendhack, Lusiane M.; Touyz, Rhian M.; Tirapelli, Carlos R.
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

24/09/2013

24/09/2013

01/01/2012

Resumo

We investigated the role of reactive oxygen species (ROS) and nitric oxide (NO) in ethanol-induced relaxation. Vascular reactivity experiments showed that ethanol (0.03-200 mmol/L) induced relaxation in endothelium-intact and denuded rat aortic rings isolated from male Wistar rats. Pre-incubation of intact or denuded rings with L-NAME (non selective NOS inhibitor, 100 mu mol/L), 7-nitroindazole (selective nNOS inhibitor, 100 mu mol/L), ODQ (selective inhibitor of guanylyl cyclase enzyme, I mu mol/L), glibenclamide (selective blocker of ATP-sensitive K+ channels, 3 mu mol/L) and 4-aminopyridine (selective blocker of voltage-dependent K+ channels, 4-AP, 1 mmol/L) reduced ethanol-induced relaxation. Similarly, tiron (superoxide anion (O-2(-)) scavenger, 1 mmol/L) and catalase (hydrogen peroxide (H2O2) scavenger, 300 U/mL) reduced ethanol-induced relaxation to a similar extent in both endothelium-intact and denuded rings. Finally, prodifen (non-selective cytochrome P450 enzymes inhibitor, 10 mu mol/L) and 4-methylpyrazole (selective alcohol dehydrogenase inhibitor, 10 mu mol/L) reduced ethanol-induced relaxation. In cultured aortic vascular smooth muscle cells (VSMCs), ethanol stimulated generation of NO, which was significantly inhibited by L-NAME. In endothelial cells, flow cytometry studies showed that ethanol increased cytosolic Ca2+ concentration ([Ca2+]c), O-2(-) and cytosolic NO concentration ([NO]c). Tiron inhibited ethanol-induced increase in [Ca-2]c and [NO]c. The major new finding of this work is that ethanol induces relaxation via redox-sensitive and NO-cGMP-dependent pathways through direct effects on ROS production and NO signaling. These findings identify putative molecular mechanisms whereby ethanol, at pharmacological concentrations, influences vascular reactivity. (C) 2011 Elsevier Inc. All rights reserved.

Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP)

Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP) [06/60076-7]

Canadian Institute of Health Research (CIHR) [44018]

Canadian Institute of Health Research (CIHR)

HSFC

HSFC

Canada Research Chair/Canadian Foundation for Innovation

Canada Research Chair/Canadian Foundation for Innovation

Identificador

VASCULAR PHARMACOLOGY, NEW YORK, v. 56, n. 41306, pp. 74-83, JAN-FEB, 2012

1537-1891

http://www.producao.usp.br/handle/BDPI/33646

10.1016/j.vph.2011.11.006

http://dx.doi.org/10.1016/j.vph.2011.11.006

Idioma(s)

eng

Publicador

ELSEVIER SCIENCE INC

NEW YORK

Relação

VASCULAR PHARMACOLOGY

Direitos

openAccess

Copyright ELSEVIER SCIENCE INC

Palavras-Chave #ETHANOL #AORTA #RELAXATION #NITRIC OXIDE #REACTIVE OXYGEN SPECIES #AORTIC ENDOTHELIAL-CELLS #CORONARY-HEART-DISEASE #HYDROGEN-PEROXIDE #BLOOD-PRESSURE #ALCOHOL-CONSUMPTION #SMOOTH-MUSCLE #PHOSPHOLIPASE A(2) #SUPEROXIDE #ACTIVATION #SYNTHASE #PHARMACOLOGY & PHARMACY
Tipo

article

original article

publishedVersion