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阿片类药物对未接触过药物及耐受大鼠皮层单单位活动的作用。

Actions of opiates upon single unit activity in the cortex of naive and tolerant rats.

作者信息

Satoh M, Zieglgänsberger W, Herz A

出版信息

Brain Res. 1976 Oct 8;115(1):99-110. doi: 10.1016/0006-8993(76)90825-8.

Abstract

The effect of microelectrophoretically and systemically applied opiates on neuronal discharge activity in the sensorimotor cortex of naive and morphine tolerant/dependent rats has been studied. In naive rats depression of spontaneous discharge activity was the predominant effect of low doses of phoretically applied morphine. Higher doses and repeated application frequently converted this effect into excitation. Only the depressant effect was antagonised by naloxone. Naloxone itself had no effect on spontaneous discharge activity when applied at dose-levels sufficient to antagonise the depressant effect of morphine. Levorphanol mimicked the action of morphine whereas dextrorphan was inactive. Morphine depressed the excitatory action of L-glutamate and of acetylcholine by a naloxone-antagonisable mechanism. Systemic application of Fentanyl mimicked the inhibitory effect of phoretically applied morphine upon transcallosally evoked discharge activity. The late response was markedly depressed whereas the primary response was little affected. Phoretically applied naloxone antagonised the effects of systemically applied Fentanyl. In chronically morphinised rats the depressant effect of microelectrophoretically administered morphine was almost lacking and a naloxone-resistant excitation became the predominant effect. In these animals the excitant effect of naloxone was also increased and the anti-glutamate effect and the anti-acetylcholine effect of morphine was abolished. The present data speak in favour of a postsynaptically located stereospecific receptor which mediates the inhibitory effects of opiates and which may be involved in the development of acute and chronic tolerance to these drugs.

摘要

研究了微电泳法和全身给药的阿片类药物对未接触过吗啡及吗啡耐受/依赖大鼠感觉运动皮层神经元放电活动的影响。在未接触过吗啡的大鼠中,低剂量微电泳给予吗啡的主要作用是抑制自发放电活动。较高剂量及重复给药时,这种作用常转变为兴奋。只有抑制作用能被纳洛酮拮抗。当给予足以拮抗吗啡抑制作用剂量的纳洛酮时,其本身对自发放电活动无影响。左啡诺模拟吗啡的作用,而右啡烷无活性。吗啡通过一种可被纳洛酮拮抗的机制抑制L-谷氨酸和乙酰胆碱的兴奋作用。全身给予芬太尼模拟了微电泳给予吗啡对经胼胝体诱发的放电活动的抑制作用。晚期反应明显受到抑制,而初级反应影响较小。微电泳给予纳洛酮可拮抗全身给予芬太尼的作用。在慢性给予吗啡的大鼠中,微电泳给予吗啡的抑制作用几乎消失,一种对纳洛酮耐受的兴奋作用成为主要作用。在这些动物中,纳洛酮的兴奋作用也增强,吗啡的抗谷氨酸和抗乙酰胆碱作用消失。目前的数据支持存在一种位于突触后、介导阿片类药物抑制作用的立体特异性受体,且该受体可能参与对这些药物急性和慢性耐受性的形成。

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