1. Academic Validation
  2. Riboflavin reduces hyperalgesia and inflammation but not tactile allodynia in the rat

Riboflavin reduces hyperalgesia and inflammation but not tactile allodynia in the rat

  • Eur J Pharmacol. 2004 May 10;492(1):35-40. doi: 10.1016/j.ejphar.2004.03.043.
Vinicio Granados-Soto 1 Flavio Terán-Rosales Héctor I Rocha-González Gerardo Reyes-García Roberto Medina-Santillán Juan Rodríguez-Silverio Francisco J Flores-Murrieta
Affiliations

Affiliation

  • 1 Departamento de Farmacobiología, Centro de Investigación y de Estudios Avanzados del Instituto Politécnico Nacional, Calzada Tenorios 235, Colonia Granjas Coapa, 14330 México, DF, Mexico. [email protected]
Abstract

Vitamin B2 (riboflavin) has been proposed as a prophylactic therapy of migraine. However, so far there are no preclinical studies about the analgesic properties of this vitamin. The current study was designed to investigate the possible antinociceptive, antihyperalgesic and antiallodynic effect of riboflavin in formalin, carrageenan-induced thermal hyperalgesia, and spinal nerve ligation models, respectively. Oral riboflavin produced a dose-related antinociceptive (6.25-50 mg/kg), antihyperalgesic (25-150 mg/kg) and anti-inflammatory (50-150 mg/kg) effect. Gabapentin (100 mg/kg, positive control), but not riboflavin (150-600 mg/kg), reduced tactile allodynia in neuropathic rats. Riboflavin-induced antinociception in the formalin test was reversed by pretreatment with NG-L-nitro-arginine methyl ester and glibenclamide, but not by NG-D-nitro-arginine methyl ester or naloxone. Our results indicate that riboflavin is able to produce antinociception and anti-inflammatory, but not antiallodynic, effect in the rat. The effect of riboflavin could be due to the activation of K+ channels or nitric oxide release, but not activation of opioid mechanisms.

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