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|Title in Portuguese:||Peripheral antinociceptive action of mangiferin in mouse models of experimental pain : role of endogenous opioids, K ATP -channels and adenosine|
|Author:||Lopes, Synara C.|
Silva, Ana Virgínia Lima da
Arruda, Bruno Rodrigues
Morais, Talita Cavalcante
Rios, Jeison Barros Rios
Trevisan, Maria Teresa Salles
Rao, Vietla Satyanarayana
Santos, Flávia A.
|Publisher:||Pharmacology, biochemistry and behavior|
|Citation:||LOPES, S. C. et al. Peripheral antinociceptive action of mangiferin in mouse models of experimental pain : role of endogenous opioids, KATP-channels and adenosine. Pharmacology, biochemistry and behavior, Fayetteville, Ark., v. 110, p. 19-26, jun. 2013.|
|Abstract:||his study aimed to assess the possible systemic antinociceptive activity of mangiferin and to clarify the un- derlying mechanism, using the acute models of chemical (acetic acid, formalin, and capsaicin) and thermal (hot-plate and tail- fl ick) nociception in mice. Mangiferin at oral doses of 10 to 100 mg/kg evidenced signif- icant antinociception against chemogenic pain in the test models of acetic acid-induced visceral pain and in formalin- and capsaicin-induced neuro-in fl ammatory pain, in a naloxone-sensitive manner, suggesting the participation of endogenous opiates in its mechanism. In capsaicin test, the antinociceptive effect of mangiferin (30 mg/kg) was not modi fi ed by respective competitive and non-competitive transient receptor potential vanilloid 1 (TRPV1) antagonists, capsazepine and ruthenium red, or by pretreatment with L -NAME, a non-selective nitric oxide synthase inhibitor, or by ODQ, an inhibitor of soluble guanylyl cyclase. However, mangiferin effect was signi fi cantly reversed by glibenclamide, a blocker of K ATP channels and in animals pretreated with 8-phenyltheophylline, an adenosine receptor antagonist. Mangiferin failed to modify the thermal nociception in hot-plate and tail- fl ick test models, suggesting that its analgesic effect is only periph- eral but not central. The orally administered mangiferin (10 – 100 mg/kg) was well tolerated and did not im- pair the ambulation or the motor coordination of mice in respective open- fi eld and rota-rod tests, indicating that the observed antinociception was unrelated to sedation or motor abnormality. The fi ndings of this study suggest that mangiferin has a peripheral antinociceptive action through mechanisms that involve endoge- nous opioids, K ATP -channels and adenosine receptors|
|metadata.dc.type:||Artigo de Periódico|
|Appears in Collections:||DFIFA - Artigos publicados em revista científica|
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