Anti-nociceptive effect of vitexin mediated by the opioid system in mice


DEMİR ÖZKAY Ü., CAN Ö. D.

PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, cilt.109, ss.23-30, 2013 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 109
  • Basım Tarihi: 2013
  • Doi Numarası: 10.1016/j.pbb.2013.04.014
  • Dergi Adı: PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.23-30
  • Anahtar Kelimeler: Anti-nociceptive, Vitexin, Opioid, Hot-plate test, Tail-clip test, Acetic acid-induced writhing test, ALPHA-GLUCOSIDASE INHIBITORS, ANTIINFLAMMATORY ACTIVITIES, ANIMAL-MODELS, TUMOR-GROWTH, EXTRACT, PAIN, FLAVONOIDS, INVOLVEMENT, RECEPTOR, HAWTHORN
  • Anadolu Üniversitesi Adresli: Evet

Özet

In the present study, we determined the potential anti-nociceptive activity of vitexin, a C-glycosylated flavone, by conducting some acute nociceptive tests in mice. Centrally mediated anti-nociceptive effect was evaluated by hot-plate and tail-clip tests, whereas peripherally mediated anti-nociception was assessed by acetic acid-induced writhing tests. Rota-rod test was performed to evaluate the probable effect of vitexin on the motor coordination of mice. Vitexin administered orally at doses of 10, 20, and 30 mg/kg significantly increased the reaction times of animals in the hot-plate and tail-clip tests and reduced the number of acetic acid-induced writhes and stretches in writhing tests, which clearly indicated the presence of the anti-nociceptive effect. This effect disappeared by pretreatment with naloxone (a non-selective opioid receptor antagonist, 5.48 mg/kg, i.p.), which indicated the involvement of opioid mechanisms in anti-nociception. We evaluated the contribution of mu, delta, and kappa subtypes of opioid receptors to the anti-nociceptive activity by using naloxonazine (7 mg/kg, s.c.), naltrindole (0.99 mg/kg, i.p.), and nor-binaltorphimine (1.03 mg/kg, i.p.), respectively. Pretreatment using these antagonists reversed the anti-nociceptive effect of vitexin in all the nociceptive tests, which indicated that mu, delta, and kappa opioid receptors contributed to the anti-nociceptive effect of this flavonoid. Falling latencies of mice in the Rota-rod test did not change upon the administration of vitexin, which indicated that vitexin showed specific anti-nociceptive effect. To the best of our knowledge, this is the first study on centrally and peripherally mediated anti-nociceptive effect of vitexin via opioid-related mechanisms. (C) 2013 Elsevier Inc. All rights reserved.