Comparison of the antinociceptive effect of celecoxib, diclofenac and resveratrol in the formalin test

被引:69
|
作者
Torres-López, JE
Ortiz, MI
Castañeda-Hernández, G
Alonso-López, R
Asomoza-Espinosa, R
Granados-Soto, V
机构
[1] Inst Politecn Nacl, Ctr Invest & Estudios Avanzados, Dept Farmacol, Mexico City 14330, DF, Mexico
[2] Univ Juarez Autonoma Tabasco, Div Acad Ciencias Salud, Ctr Invest & Posgrado, Tabasco, Mexico
[3] Inst Politecn Nacl, Ctr Invest & Estudios Avanzados, Secc Externa Farmacol, Mexico City, DF, Mexico
[4] Univ Autonoma Estado Hidalgo, Inst Ciencias Salud, Area Acad Med, Hidalgo, Mexico
关键词
celecoxib; diclofenac; resveratrol; cyclooxygenase; 1; 2; inflammatory pain;
D O I
10.1016/S0024-3205(02)01491-1
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The peripheral antinociceptive effect of the selective COX-2 inhibitor celecoxib in the formalin-induced inflammatory pain was compared with that of resveratrol (COX-1 inhibitor) and diclofenac (non-selective COX inhibitor). Rats received local pretreatment with saline, celecoxib, diclofenac or resveratrol followed by 50 mul of either 1% or 5% formalin. Peripheral administration of celecoxib did not produce antinociception at either formalin concentration. In contrast, diclofenac and resveratrol produced a dose-dependent antinociceptive effect in the second phase of both 1% and 5% formalin test. The peripheral antinociception produced by diclofenac or resveratrol was due to a local action, as drug administration in the contralateral paw was ineffective. Results indicate that the selective COX-2 inhibitor celecoxib does not produce peripheral antinociception in formalin-induced inflammatory pain. In contrast, selective COX-1 and non-selective COX inhibitors (resveratrol and diclofenac, respectively) are effective drugs in this model of pain. (C) 2002 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:1669 / 1676
页数:8
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