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S. García-Muñoz, Míriam Álvarez-Corral, Leticia Jiménez-González, C. López-Sánchez, Antonio Rosales, M. Muñoz-Dorado, I. Rodríguez‐García (2006)
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The antinociceptive activity of icariside E 4 , a dihydrobenzofuran-type lignan isolated from Tabebuia roseo - alba (Ridley) Sandwith (Bignoniaceae) bark, was evaluated in mice by using chemical and thermal models of nociception. Intraperitoneal (i.p.) administration of crude T. roseo - alba bark extract and its methanol fraction inhibited acetic acid-induced abdominal constriction in mice. Furthermore, i.p. administration of 0.1, 1, and 10 mg/kg of icariside E 4 reduced the number of writhes evoked by acetic acid injection by 46.9, 82.3, and 66.6 %, respectively. Icariside E 4 administration had no effect in the first phase of the formalin test, but it reduced nociceptive behavior in the second phase as indicated by a reduction in the licking time. Icariside E 4 did not modify thermal nociception in the hot-plate test model, suggesting that it had a peripheral antinociceptive action. The antinociceptive effect of icariside E 4 in the writhing test was reversed by pre-administration of glibenclamide, but not of naloxone, atropine, yohimbine, or haloperidol. Together, these results indicated that the antinociceptive activity of icariside E 4 from T. roseo - alba in models of chemical pain occurred through ATP-sensitive K + channel-dependent mechanisms.
Archives of Pharmacal Research – Springer Journals
Published: Jun 1, 2015
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