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PMID: 12467522 Published · ppublish English Journal Article

Effects of methotrexate upon inflammatory parameters induced by carrageenan in the mouse model of pleurisy.

Mediators of inflammation ·Vol. 11 ·No. 5 ·2002-10-00 ·Pages 299-306

Dalmarco EM, Fröde TS, Medeiros YS

Abstract

The model of pleurisy induced by carrageenan exhibits a biphasic response (4 and 48 h) and permits the quantification of exudate, cell migration and certain enzymes such as myeloperoxidase (MPO) and adenosine-deaminase (ADA) that are markers of activated leukocytes. The present study evaluates whether there exists, in the pleurisy model, a significant inhibition of ADA and MPO enzymes, leukocyte kinetics and other markers of inflammation [nitric oxide (NO) levels, exudation] caused by methotrexate treatment by the intraperitoneal (i.p.) route. The pleurisy was induced by carrageenan (1%) in mice, and the parameters were analyzed 4 and 48 h after. After the induction of inflammation (4 h), methotrexate (20 mg/kg, i.p., 24 h before pleurisy induction) inhibited the leukocyte infiltration (p < 0.05), NO levels and MPO activity (p < 0.01), but not ADA activity and fluid leakage (p > 0.05). Regarding the second phase of pleurisy (48 h), methotrexate (40 mg/kg, i.p., 0.5 h before pleurisy induction) inhibited the leukocyte infiltration (p < 0.05), fluid leakage, NO levels (p < 0.01), and ADA and MPO activity (p < 0.05). These findings support the evidence that the acute administration of methotrexate has an important systemic anti-inflammatory activity in the studied inflammatory model. This effect was due to a significant inhibition on both neutrophil and mononuclear cells, being less marked in relation to exudation 48 h after. In relation to the enzymes studied and to NO levels, the findings support the evidence that methotrexate inhibits both enzymes (MPO and ADA) from leukocytes at the site of injury, thus reflecting the activation of both neutrophils and lymphocytes, respectively. Furthermore, the inhibiting effect on NO in both phases of pleurisy induced by carrageenan (4 and 48 h) indicates that methotrexate acts on constitutive and/or inducible NO synthases by means of different cells of the pleural cavity.

MeSH Terms
Adenosine Deaminase/metabolism Animals Carrageenan Disease Models, Animal Female Immunosuppressive Agents/pharmacology Male Methotrexate/pharmacology Mice Nitric Oxide/metabolism Peroxidase/metabolism Pleura/enzymology,immunology Pleurisy/chemically induced,drug therapy,immunology
Chemicals
Immunosuppressive Agents Nitric Oxide Carrageenan Peroxidase Adenosine Deaminase Methotrexate
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Dalmarco Eduardo Monguilhott
Department of Clinical Analysis, Center of Health Sciences, Universidade Federal de Santa Catarina, Campus Universitário-Trindade, 88040-970, Florianópolis, SC, Brazil.
Fröde Tânia Silvia
Medeiros Yara Santos
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Article Info
Journal
Mediators of inflammation
Abbr.
Mediators Inflamm
ISSN
0962-9351
Published
2002-10-00
Pages
299-306
Language
English
Region
United States
NLM ID
9209001
PMCID
PMC1781680
Subset
IM
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