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Differential involvement of opioid receptors in intrathecal butorphanol-induced analgesia: compared to morphine.

作者信息

Wongchanapai W, Tsang B K, He Z, Ho I K

机构信息

Department of Pharmacology and Toxicology, University of Mississippi Medical Center, Jackson 39216, USA.

出版信息

Pharmacol Biochem Behav. 1998 Mar;59(3):723-7. doi: 10.1016/s0091-3057(97)00558-3.

Abstract

The present experiments were performed to investigate the differential involvement of the opioid receptor subtypes in the antinociception of intrathecal (IT) butorphanol compared to IT morphine. A single dose (26 nmol) of IT nor-binaltorphimine (nor-BNI), beta-funaltrexamine (beta-FNA), and naltrindole (NTI) demonstrated a significant attenuation in the overall antinociception of IT butorphanol (52 nmol) or IT morphine (26 nmol). However, IT butorphanol elicits thermal antinociceptive effect through kappa > delta > or = mu, whereas morphine acts on mu >delta >> kappa. These results indicate that the antinociceptive effect of both IT butorphanol and IT morphine are mediated through mu, delta, and kappa opioid receptors in different relative orders.

摘要

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