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

被引:17
|
作者
Wongchanapai, W
Tsang, BK
He, Z
Ho, IK
机构
[1] Univ Mississippi, Med Ctr, Dept Pharmacol & Toxicol, Jackson, MS 39216 USA
[2] Univ Mississippi, Med Ctr, Dept Anesthesiol, Jackson, MS 39216 USA
关键词
antinociceptive; butorphanol; intrathecal; morphine;
D O I
10.1016/S0091-3057(97)00558-3
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
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 greater than or equal to 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. (C) 1998 Elsevier Science Inc.
引用
收藏
页码:723 / 727
页数:5
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