Different mechanisms underlie the effects of acute and long-term inhibition of nitric oxide synthases in antigen-induced pulmonary eosinophil recruitment in BALB/C mice


Autoria(s): LINTOMEN, Leticia; SOUZA-FILHO, Luis Gustavo; FERREIRA, Tatiane; CAMARGO, Enilton A.; TEIXEIRA, Simone A.; MUSCARA, Marcelo N.; LANDGRAF, Richardt G.; JANCAR, Sonia; MENDES, Gustavo D.; NUCCI, Gilberto De; ANTUNES, Edson
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

20/10/2012

20/10/2012

2009

Resumo

Nitric oxide synthase (NOS) inhibitors are largely used to evaluate the NO contribution to pulmonary allergy, but contrasting data have been reported. In this study, pharmacological, biochemical and pharmacokinetic assays were performed to compare the effects of acute and long-term treatment of BALB/C mice with the non-selective NOS inhibitor L-NAME in ovalbumin (OVA)-challenged mice. Acute L-NAME treatment (50 mg/kg, gavage) significantly reduced the eosinophil number in bronchoalveolar lavage fluid (BALF). The inducible NOS (iNOS) inhibitor aminoguanidine (20 mg/kg/day in the drinking water) also significantly reduced the eosinophil number in BALF In contrast, 3-week L-NAME treatment (50 and 150 mg/kg/day in the drinking water) significantly increased the pulmonary eosinophil influx. The constitutive NOS (cNOS) activity in brain and lungs was reduced by both acute and 3-week L-NAME treatments. The pulmonary iNOS activity was reduced by acute L-NAME (or aminoguanidine), but unaffected by 3-week L-NAME treatment. Acute L-NAME (or aminoguanidine) treatment was more efficient to reduce the NO(x) levels compared with 3-week L-NAME treatment. The pharmacokinetic study revealed that L-NAME is not bioavailable when given orally. After acute L-NAME intake, serum concentrations of the metabolite N(omega)-nitro-L-arginine decreased from 30 min to 24 h. In the 3-week L-NAME treatment, the N(omega)-nitro-L-arginine concentration was close to the detection limit. In conclusion, 3-week treatment with L-NAME yields low serum N(omega)-nitro-L-arginine concentrations, causing preferential inhibition of cNOS activity. Therefore, eosinophil influx potentiation by 3-week L-NAME treatment may reflect removal of protective cNOS-derived NO, with no interference on the ongoing inflammation due to iNOS-derived NO. (c) 2008 Elsevier Ltd. All rights reserved.

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

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

Identificador

PULMONARY PHARMACOLOGY & THERAPEUTICS, v.22, n.1, p.1-8, 2009

1094-5539

http://producao.usp.br/handle/BDPI/28313

10.1016/j.pupt.2008.10.003

http://dx.doi.org/10.1016/j.pupt.2008.10.003

Idioma(s)

eng

Publicador

ACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD

Relação

Pulmonary Pharmacology & Therapeutics

Direitos

restrictedAccess

Copyright ACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD

Palavras-Chave #Eosinophil #Nitric oxide synthase #L-NAME #Bioavailability #Eotaxin #IgE #INDUCED AIRWAY INFLAMMATION #ALLERGIC INFLAMMATION #EOTAXIN LEVEL #MURINE MODEL #BONE-MARROW #GUINEA-PIGS #L-ARGININE #IN-VITRO #ASTHMA #CHEMOKINES #Pharmacology & Pharmacy #Respiratory System
Tipo

article

original article

publishedVersion