Author(s):
Lima, Flávia Oliveira de ; Alves, Vivian ; Barbosa Filho, José Maria ; Almeida, Jackson Roberto Guedes da Silva ; Rodrigues, Luis Cezar ; Soares, Milena Botelho Pereira ; Villarreal, Cristiane Flora ; Lima, Flávia Oliveira de ; Alves, Vivian ; Barbosa Filho, José Maria ; Almeida, Jackson Roberto Guedes da Silva ; Rodrigues, Luis Cezar ; Soares, Milena Botelho Pereira ; Villarreal, Cristiane Flora
Date: 2014
Origin: Oasisbr
Subject(s): Lonchocarpus araripensis; Lupeol; Antinociception; Inflammatory pain; Post-operative pain; Cytokines
Description
Texto completo: acesso restrito. p. 1557–1563
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The present study investigates the antinociceptive properties of lupeol in models of inflammatory and post-operative pain, as well as its mechanisms of action. The effects of lupeol were tested against acetic acid-induced writhing, formalin test, carrageenan-induced hyperalgesia, and post-operative pain model. Cytokine levels were determined by ELISA. Mice motor performance was evaluated in the rota rod and open-field tests. Pre-treatment of mice with lupeol (5–100 mg/kg IP) produced a dose-related inhibition of writhing in mice. The maximal antinociception produced by lupeol (60 mg/kg) was unaffected in mice pre-treated with yohimbine (α2 adrenoceptor antagonist; 2 mg/kg IP), L-arginine (substrate for nitric oxide synthase; 600 mg/kg IP), glibenclamide (the KATP-channel blocker; 2 mg/kg IP), and methysergide maleate (serotoninergic receptors antagonist; 5 mg/kg IP). Furthermore, lupeol (25–100 mg/kg) inhibited the late phase of formalin test. Pre-treatment with lupeol (50 and 100 mg/kg) inhibited the hyperalgesia and the local increase in tumor necrosis factor-α (TNF-α) and interleukin-1β (IL-1β) levels induced by carrageenan. In contrast, lupeol did not inhibit the post-operative pain. Lupeol-treated mice did not show any motor performance alterations or apparent systemic toxicity. Our results demonstrate that lupeol has consistent antinociceptive properties during inflammatory pain, but not post-operative pain, acting through the inhibition of IL-1β and TNF-α production.
