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Attenuation of spontaneous opiate withdrawal in mice by the anandamide transport inhibitor AM404.

作者信息

Del Arco Ignacio, Navarro Miguel, Bilbao Ainhoa, Ferrer Belén, Piomelli Daniele, Rodríguez De Fonseca Fernando

机构信息

Fundación Hospital Carlos Haya, Avda Carlos Haya 82. 7 Planta, Pabellón A., Málaga 29010, Spain.

出版信息

Eur J Pharmacol. 2002 Nov 1;454(1):103-4. doi: 10.1016/s0014-2999(02)02483-4.

DOI:10.1016/s0014-2999(02)02483-4
PMID:12409011
Abstract

The endogenous cannabinoid, anandamide, has been shown to attenuate naloxone-precipitated opiate withdrawal in rodents. Here we show that the spontaneous, but not the naloxone-precipitated withdrawal syndrome in morphine-dependent mice is attenuated by the inhibitor of carrier-mediated anandamide transport N-(4-hydroxyphenyl) arachidonylethanolamide (AM404) (2 and 10 mg/kg, i.p.). These results suggest that spontaneous but not opioid antagonist-precipitated withdrawal is associated with dynamic changes in endogenous cannabinoid signaling.

摘要

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