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长期使用吗啡治疗后自发撤药会加速大鼠脑内α2-肾上腺素能受体的更新:受体出现增加相关的受体上调。

Spontaneous withdrawal from long-term treatment with morphine accelerates the turnover of alpha 2-adrenoceptors in the rat brain: up-regulation of receptors associated with increased receptor appearance.

作者信息

Gabilondo A M, García-Sevilla J A

机构信息

Department of Pharmacology, Faculty of Medicine, University of the Basque Country, Leioa, Bizkaia.

出版信息

J Neurochem. 1995 Jun;64(6):2590-7. doi: 10.1046/j.1471-4159.1995.64062590.x.

DOI:10.1046/j.1471-4159.1995.64062590.x
PMID:7760039
Abstract

The aim of this study was to quantify and compare the turnover of brain alpha 2-adrenoceptors during chronic morphine treatment and after spontaneous morphine withdrawal in rats. The oral administration of increasing doses of morphine (10-90 mg/kg) for 20 days did not alter the specific binding of the agonist [3H]-clonidine in the cerebral cortex. However, spontaneous opiate withdrawal (24 h) significantly increased the density of cortical alpha 2-adrenoceptors (Bmax for [3H]clonidine was 21% greater). The recovery of [3H]clonidine binding after irreversible inactivation by N-ethoxycarbonyl-2-ethoxy-1,2- dihydroquinoline (1.6 mg/kg) was assessed in naive, morphine-dependent, and morphine-withdrawn rats to study the process of alpha 2-adrenoceptor repopulation and to calculate receptor turnover parameters. The simultaneous analysis of receptor recovery curves revealed that the turnover of brain alpha 2-adrenoceptors in morphine-withdrawn rats was accelerated [appearance rate constant (r) = 21 fmol/mg of protein/day; disappearance rate constant (k) = 0.25 day-1] compared with those in morphine-dependent (r = 13 fmol/mg of protein/day; k = 0.14 day-1) and naive (r = 15 fmol/mg of protein/day; k = 0.16 day-1) rats. Moreover, this analysis also indicated that the increased density of cortical alpha 2-adrenoceptors observed during morphine withdrawal was due to a significantly higher receptor appearance (delta r = 37-57%) and not to a decreased receptor disappearance, which in fact showed also an increase (delta k = 56-79%).(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

本研究的目的是量化并比较大鼠慢性吗啡治疗期间及自发吗啡戒断后脑α2-肾上腺素能受体的更新情况。连续20天口服递增剂量的吗啡(10 - 90毫克/千克)未改变激动剂[3H] - 可乐定在大脑皮层的特异性结合。然而,自发阿片戒断(24小时)显著增加了皮层α2-肾上腺素能受体的密度([3H]可乐定的Bmax增加了21%)。通过N - 乙氧羰基 - 2 - 乙氧基 - 1,2 - 二氢喹啉(1.6毫克/千克)不可逆失活后,评估了未用吗啡的、吗啡依赖的和吗啡戒断的大鼠中[3H]可乐定结合的恢复情况,以研究α2-肾上腺素能受体再填充过程并计算受体更新参数。对受体恢复曲线的同步分析显示,与吗啡依赖(r = 13飞摩尔/毫克蛋白质/天;k = 0.14天-1)和未用吗啡的(r = 15飞摩尔/毫克蛋白质/天;k = 0.16天-1)大鼠相比,吗啡戒断大鼠脑α2-肾上腺素能受体的更新加速(出现速率常数[r] = 21飞摩尔/毫克蛋白质/天;消失速率常数[k] = 0.25天-1)。此外,该分析还表明,吗啡戒断期间观察到的皮层α2-肾上腺素能受体密度增加是由于受体出现显著增加(δr = 37 - 57%),而非受体消失减少,实际上受体消失也有所增加(δk = 56 - 79%)。(摘要截选于250字)

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