Nitroxides attenuate carrageenan-induced inflammation in rat paws by reducing neutrophil infiltration and the resulting myeloperoxidase-mediated damage


Autoria(s): Queiroz, Raphael F.; Jordao, Alessandro K.; Cunha, Anna C.; Ferreira, Vitor F.; Brigagao, Maisa R. P. L.; Malvezzi, Alberto; Amaral, Antonia Tavares do; Augusto, Ohara
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

06/11/2013

06/11/2013

2012

Resumo

Tempol (4-hydroxy-2,2,6,6-tetramethylpiperidine-1-oxyl) and other cyclic nitroxides have been shown to inhibit the chlorinating activity of myeloperoxidase (MPO) in vitro and in cells. To examine whether nitroxides inhibit MPO activity in vivo we selected acute carrageenan-induced inflammation on the rat paw as a model. Tempol and three more hydrophobic 4-substituted derivatives (4-azido, 4-benzene-Sulfonyl, and 4-(4-phenyl-1H-1,2,3-triazol-1-yl)) were synthesized, and their ability to inhibit the in vitro chlorinating activity of MPO and carrageenan-induced inflammation in rat paws was evaluated. All of the tested nitroxides inhibited the chlorinating activity of MPO in vitro with similar IC50 values (between 1.5 and 1.8 mu M). In vivo, the attenuation of carrageenan-induced inflammation showed some correlation with the lipophilicity of the nitroxide at early time points but the differences in the effects were small (< 2-fold) compared with the differences in lipophilicity (> 200-fold). No inhibition of MPO activity in vivo was evident because the levels of MPO activity in rat paws correlated with the levels of MPO protein'. Likewise, paw edema, levels of nitrated and oxidized proteins, and levels of plasma exudation correlated with the levels of MPO protein in the paws of the animals that were untreated or treated with the nitroxides. The effects of the nitroxides in vivo were compared with those of 4-aminobenzoic hydrazide and of colchicine. Taken together, the results indicate that nitroxides attenuate carrageenan-induced inflammation mainly by reducing neutrophil migration and the resulting MPO-mediated damage. Accordingly, tempol was shown to inhibit rat neutrophil migration in vitro. (C) 2012 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)

Conselho Nacional de Desenvolvimento Cientifico Tecnologico (CNPq)

Conselho Nacional de Desenvolvimento Cientifico Tecnologico (CNPq)

Coordenacao de Aperfeicoamento de Pessoal de Nivel Superior (CAPES)

Coordenacao de Aperfeicoamento de Pessoal de Nivel Superior (CAPES)

Identificador

FREE RADICAL BIOLOGY AND MEDICINE, NEW YORK, v. 53, n. 10, pp. 1942-1953, 42309, 2012

0891-5849

http://www.producao.usp.br/handle/BDPI/42175

10.1016/j.freeradbiomed.2012.09.001

http://dx.doi.org/10.1016/j.freeradbiomed.2012.09.001

Idioma(s)

eng

Publicador

ELSEVIER SCIENCE INC

NEW YORK

Relação

FREE RADICAL BIOLOGY AND MEDICINE

Direitos

closedAccess

Copyright ELSEVIER SCIENCE INC

Palavras-Chave #INFLAMMATION #NEUTROPHILS #MYELOPEROXIDASE #NITROXIDES #4-AMINOBENZOIC HYDRAZIDE #NITROXIDE LIPOPHILICITY #NEUTROPHIL MIGRATION #OXIDATIVE DAMAGE #FREE RADICALS #PERMEABLE RADICAL SCAVENGER #NITRIC-OXIDE #TYROSINE NITRATION #ANTIOXIDANT DEFENSE #CYCLIC NITROXIDES #THIYL RADICALS #TEMPOL #INHIBITION #PROTEINS #MECHANISM #BIOCHEMISTRY & MOLECULAR BIOLOGY #ENDOCRINOLOGY & METABOLISM
Tipo

article

original article

publishedVersion