Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/63810
Type: Artigo de periódico
Title: EFFECT OF CHRONIC NITRIC-OXIDE SYNTHESIS INHIBITION ON THE INFLAMMATORY RESPONSES INDUCED BY CARRAGEENAN IN RATS
Author: MEDEIROS, MV
BINHARA, IM
MORENO, H
ZATZ, R
DENUCCI, G
ANTUNES, E
Abstract: The effect of chronic inhibition of nitric oxide (NO) biosynthesis has been investigated in two models of acute inflammation induced by carrageenin, i.e., paw oedema and pleurisy. Chronic inhibition of NO biosynthesis was achieved by including N-omega-nitro-L-arginine methyl ester (L-NAME) in the drinking water to give a dose of approximately 75 mu mol/rat/day for 2 and 4 weeks. Control animals received either tap water alone or the inactive enantiomer D-NAME. Since chronic NO inhibition increases blood pressure, rats made hypertensive (2 kidney-1 clip model; 2K-1C) were used to evaluate the effect of hypertension on the carrageenin-induced paw oedema. In a separate set of experiments, L-NAME-treated animals concomitantly received captopril (140 mu mol/rat/day) to prevent hypertension. Animals chronically treated with L-NAME (but not D-NAME) for 2 and 4 weeks developed hypertension to the same extent as 2K-1C rats. Carrageenin-induced paw oedema was significantly reduced in animals chronically treated with L-NAME, but not with D-NAME or in 2K-1C rats. Subplantar injection of iloprost completely reversed the inhibition of paw oedema caused by L-NAME. Captopril (140 mu mol/rat/day) significantly lowered the high blood pressure levels induced by L-NAME but did not significantly affect the inhibition of paw oedema caused by L-NAME. No changes in vascular permeability, as assessed by Evans blue extravasation, were observed in L-NAME-treated animals. The chronic treatment with L-NAME for 2 and 4 weeks did not inhibit carrageenin-induced leucocyte migration and fluid exudation into the pleural cavity. Although carrageenin-induced paw oedema is reduced in L-NAME-treated rats, this response reflects a decrease in local blood flow rather than an effect on vascular permeability.
Subject: ILOPROST
NITRIC OXIDE (NO)
ACUTE INFLAMMATION
CAPTOPRIL
HYPERTENSION
(2K-1C RAT)
Country: Holanda
Editor: Elsevier Science Bv
Rights: fechado
Identifier DOI: 10.1016/0014-2999(95)00332-F
Date Issue: 1995
Appears in Collections:Unicamp - Artigos e Outros Documentos

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