AJP - Regu Add DOIs to your references at manuscript stage!
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Am J Physiol Regul Integr Comp Physiol 296: R1631-R1640, 2009. First published February 25, 2009; doi:10.1152/ajpregu.90527.2008
0363-6119/09 $8.00
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
296/5/R1631    most recent
90527.2008v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Kanashiro, A.
Right arrow Articles by de Souza, G. E. P.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Kanashiro, A.
Right arrow Articles by de Souza, G. E. P.

TEMPERATURE AND FEVER

Characterization and pharmacological evaluation of febrile response on zymosan-induced arthritis in rats

Alexandre Kanashiro,1 Andréa C. Pessini,1 Renes R. Machado,1 David do C. Malvar,1 Fernando A. Aguiar,1 Denis Melo Soares,1 Mariana L. do Vale,2 and Glória E. Petto de Souza1

1Laboratory of Pharmacology, Faculty of Pharmaceutical Sciences, Universidade de São Paulo, Ribeirão Preto, São Paulo, Brazil; and 2Department of Physiology and Pharmacology, Faculty of Medicine, Federal University of Ceará, Fortaleza, Ceará, Brazil

Submitted 23 June 2008 ; accepted in final form 18 February 2009

The present study investigated the febrile response in zymosan-induced arthritis, as well as the increase in PGE2 concentration in the cerebrospinal fluid (CSF), along with the effects of antipyretic drugs on these responses in rats. Zymosan intra-articularly injected at the dose of 0.5 mg did not affect the body core temperature (Tc) compared with saline (control), whereas at doses of 1 and 2 mg, zymosan promoted a flattened increase in Tc and declined thereafter. The dose of 4 mg of zymosan was selected for further experiments because it elicited a marked and long-lasting Tc elevation starting at 3 1/2 h, peaking at 5 1/2 h, and remaining until 10 h. This temperature increase was preceded by a decrease in the tail skin temperature, as well as hyperalgesia and edema in the knee joint. No febrile response was observed in the following days. In addition, zymosan-induced fever was not modified by the sciatic nerve excision. Zymosan increased PGE2 concentration in the CSF but not in the plasma. Oral pretreatment with ibuprofen (5–20 mg/kg), celecoxib (1–10 mg/kg), dipyrone (60–240 mg/kg), and paracetamol (100–200 mg/kg) or subcutaneous injection of dexamethasone (0.25–1.0 mg/kg) dose-dependently reduced or prevented the fever during the zymosan-induced arthritis. Celecoxib (5 mg/kg), paracetamol (150 mg/kg), and dipyrone (120 mg/kg) decreased CSF PGE2 concentration and fever during zymosan-induced arthritis, suggesting the involvement of PGE2 in this response.

fever; anti-inflammatory drugs; paracetamol; dipyrone; celacoxib; prostaglandin E2



Address for reprint requests and other correspondence: G. E. Petto de Souza, Departamento de Física e Química, Faculdade de Ciências Farmacêuticas de Ribeirão Preto-Universidade de São Paulo. Avenida do Café s/n°., Campus USP, Ribeirão Preto, SP, Brasil, CEP 14040-903. (e-mail: gepsouza{at}fcfrp.usp.br)







HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Visit Other APS Journals Online
Copyright © 2009 by the American Physiological Society.