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纳洛酮诱发吗啡耐受/依赖大鼠脑内单神经元阿片类物质戒断反应的演示。

A demonstration of naloxone-precipitated opiate withdrawal on single neurones in the morphine-tolerant/dependent rat brain.

作者信息

Fry J P, Herz A, Zieglgänsberger W

出版信息

Br J Pharmacol. 1980 Mar;68(3):585-92. doi: 10.1111/j.1476-5381.1980.tb14574.x.

Abstract

1 A comparison has been made between the effects of microelectrophoretically applied naloxone on single neurones in the frontal cerebral cortex and the striatum of naive and of morphine-tolerant/dependent rats, anaesthetized with a mixture of alpha-chloralose and urethane. 2 Specificity of the results obtained was evaluated by contrasting the effects of alternate applications of the (+)- and (-)-isomers of naloxone to the same neurones. 3 In naive rats naloxone had predominantly no effect, only a few cells revealing non-specific depressant responses to the drug. 4 In morphine-tolerant/dependent rats a higher proportion of neurones responded to naloxone; either with stereospecific excitatory responses, in which the activity evoked by L-glutamate or acetylcholine was increased, or with a non-specific inhibition, similar to that observed in naive animals. 5 It is suggested that these excitatory responses to microelectrophoretically applied (-)-naloxone represent opiate withdrawal responses at the single neurone level and that they reflect a latent hyperexcitability of the postsynaptic membrane in the morphine-tolerant/dependent state.

摘要
  1. 对用α-氯醛糖和乌拉坦混合麻醉的未用药大鼠以及吗啡耐受/依赖大鼠的额叶皮质和纹状体中的单个神经元,进行了微电泳施加纳洛酮的效果比较。2. 通过对比向同一神经元交替施加纳洛酮的(+)-和(-)-异构体的效果,评估所得结果的特异性。3. 在未用药大鼠中,纳洛酮主要无作用,只有少数细胞对该药物表现出非特异性抑制反应。4. 在吗啡耐受/依赖大鼠中,更高比例的神经元对纳洛酮有反应;要么是立体特异性兴奋反应,其中L-谷氨酸或乙酰胆碱诱发的活性增加,要么是与未用药动物中观察到的类似的非特异性抑制。5. 提示这些对微电泳施加的(-)-纳洛酮的兴奋反应代表了单神经元水平的阿片戒断反应,并且它们反映了吗啡耐受/依赖状态下突触后膜的潜在兴奋性过高。

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