Supersensitivity of spinal opioid receptors to antagonists in intrathecal butorphanol and morphine dependence

被引:10
|
作者
Wongchanapai, W
Tsang, BK
He, Z
Ma, TG
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
intrathecal; butorphanol; morphine; physical dependence; spinal opioid receptors;
D O I
10.1016/S0024-3205(98)00498-6
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The purpose of this investigation was to evaluate changes in the sensitivity of spinal opioid receptors to selective antagonists in rats rendered dependent on intrathecal (i.t.) butorphanol and morphine. Using quantitative autoradiography, competitive binding assays with selective opioid antagonists were performed in the spinal cord sections of i.t. butorphanol- and morphine-dependent rats in which withdrawal was precipitated by i.t. naloxone. In butorphanol-dependent rats, the spinal kappa-opioid receptor developed a greater degree of antagonist supersensitivity than the spinal delta- and mu-opioid receptors did. In contrast, the spinal mu-opioid receptor became more sensitive than the delta-opioid receptor in morphine-dependent rats. These results indicate that differential supersensitivity of spinal opioid receptors was induced after chronic i.t. infusions of butorphanol and morphine.
引用
收藏
页码:2175 / 2180
页数:6
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