The role of reactive oxygen species in the modulation of the contraction induced by angiotensin II in carotid artery from diabetic rat
Contribuinte(s) |
UNIVERSIDADE DE SÃO PAULO |
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Data(s) |
07/11/2013
07/11/2013
2012
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Resumo |
The modulation played by reactive oxygen species on the angiotensin II-induced contraction in type I-diabetic rat carotid was investigated. Concentration-response curves for angiotensin II were obtained in endothelium-intact or endothelium-denuded carotid from control or streptozotocin-induced diabetic rats, pre-treated with tiron (superoxide scavenger), PEG-catalase (hydrogen peroxide scavenger), dimethylthiourea (hydroxyl scavenger), apocynin [NAD(P) H oxidase inhibitor], SC560 (cyclooxygenase-1 inhibitor), SC236 (cyclooxygenase-2 inhibitor) or Y-27632 (Rho-kinase inhibitor). Reactive oxygen species were measured by flow cytometry in dihydroethidium (DHE)-loaded endothelial cells. Cyclooxygenase and AT1-receptor expression was assessed by immunohistochemistry. Diabetes increased the angiotensin II-induced contraction but reduced the agonist potency in rat carotid. Endothelium removal, tiron or apocynin restored the angiotensin II-induced contraction in diabetic rat carotid to control levels. PEG-catalase, DMTU or SC560 reduced the angiotensin II-induced contraction in diabetic rat carotid at the same extent. SC236 restored the angiotensin II potency in diabetic rat carotid. Y-27632 reduced the angiotensin II-induced contraction in endothelium-intact or -denuded diabetic rat carotid. Diabetes increased the DHE-fluorescence of carotid endothelial cells. Apocynin reduced the DHE-fluorescence of endothelial cells from diabetic rat carotid to control levels. Diabetes increased the muscular cyclooxygenase-2 expression but reduced the muscular AT1-receptor expression in rat carotid. In summary, hydroxyl radical, hydrogen peroxide and superoxide anion-derived from endothelial NAD(P) H oxidase mediate the hyperreactivity to angiotensin II in type I-diabetic rat carotid, involving the participation of cyclooxygenase-1 and Rho-kinase. Moreover, increased muscular cyclooxygenase-2 expression in type I-diabetic rat carotid seems to be related to the local reduced AT1-receptor expression and the reduced angiotensin II potency. (C) 2011 Elsevier B. V. All rights reserved. Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP) [2009/01005-0] Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP) Coordenacao de Aperfeicoamento de Pessoal de Nivel Superior (CAPES) Coordenacao de Aperfeicoamento de Pessoal de Nivel Superior (CAPES) Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq), Brazil Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq) (Brazil) |
Identificador |
EUROPEAN JOURNAL OF PHARMACOLOGY, AMSTERDAM, v. 678, n. 41334, supl. 1, Part 6, pp. 15-25, 38412, 2012 0014-2999 http://www.producao.usp.br/handle/BDPI/43306 10.1016/j.ejphar.2011.12.036 |
Idioma(s) |
eng |
Publicador |
ELSEVIER SCIENCE BV AMSTERDAM |
Relação |
EUROPEAN JOURNAL OF PHARMACOLOGY |
Direitos |
closedAccess Copyright ELSEVIER SCIENCE BV |
Palavras-Chave | #DIABETES MELLITUS #CAROTID ARTERY #REACTIVE OXYGEN SPECIES #ANGIOTENSIN II #ENDOTHELIUM-DEPENDENT CONTRACTIONS #INTIMA-MEDIA THICKNESS #SMOOTH-MUSCLE-CELLS #SUPEROXIDE ANION #KINASE ACTIVATION #HYPERTENSIVE-RATS #OXIDATIVE STRESS #RHO-KINASE #PHENYLEPHRINE #CHILDREN #PHARMACOLOGY & PHARMACY |
Tipo |
article original article publishedVersion |