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完整大脑的大鼠以及黑质前脑去大脑大鼠中,吗啡和其他阿片类药物诱导的黑质神经元活动变化。

Changes in the activity of nigral neurones induced by morphine and other opiates in rats with an intact brain and after prenigral decerebration.

作者信息

Jurna I

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 1981 Apr;316(2):149-54. doi: 10.1007/BF00505309.

Abstract

The effect of morphine and related opiates on the spontaneous activity of nigral neurones was studied in unanaesthetized rats with an intact brain or after prenigral decerebration. Less than 50% of the neurones were influenced by the opiates. In the intact brain, intravenous (i.v.) injection of morphine 2 mg/kg, dextrorphan 1 mg/kg and tilidine 5 mg/kg increased the discharge rate, whereas levorphanol 1 mg/kg, pethidine 20 mg/kg and codeine 10 mg/kg reduced it. Naloxone 0.2 mg/kg i.v. abolished the effects of morphine, levorphanol and codeine; it reduced the effect of pethidine and was ineffective against dextrorphan and tilidine. Intracaudate injections of morphine 10 microgram and pethidine 50 microgram increased the spontaneous activity of some neurones in the ipsilateral substantia nigra and reduced that of others; the increase in activity after morphine was more pronounced than the depression. The effects of intracaudate injections of morphine or pethidine were reduced by i.v. naloxone. After prenigral decerebration, i.v. injections of morphine depressed, and i.v. injections of levorphanol increased the activity of nigral neurones; pethidine i.v. either increased or reduced the spontaneous activity. These effects were reduced or abolished by naloxone. It is concluded that opiates including morphine affect the activity of nigral neurones not only by an action on opiate receptors in the striatum but also by an action on opiate receptors outside the striatum (e.g. in the substantia nigra and, perhaps, by an action unrelated to opiate receptors.

摘要

在未麻醉的完整大脑大鼠或黑质前脑切断术后的大鼠中,研究了吗啡及相关阿片类药物对黑质神经元自发活动的影响。不到50%的神经元受阿片类药物影响。在完整大脑中,静脉注射2mg/kg吗啡、1mg/kg右啡烷和5mg/kg替利定可增加放电率,而1mg/kg左啡诺、20mg/kg哌替啶和10mg/kg可待因则降低放电率。静脉注射0.2mg/kg纳洛酮可消除吗啡、左啡诺和可待因的作用;它可减弱哌替啶的作用,对右啡烷和替利定无效。尾状核内注射10μg吗啡和50μg哌替啶可增加同侧黑质中一些神经元的自发活动,并降低另一些神经元的自发活动;吗啡注射后活动的增加比抑制更明显。静脉注射纳洛酮可减弱尾状核内注射吗啡或哌替啶的作用。黑质前脑切断术后,静脉注射吗啡使黑质神经元活动受到抑制,而静脉注射左啡诺则增加其活动;静脉注射哌替啶可增加或降低自发活动。这些作用可被纳洛酮减弱或消除。得出的结论是,包括吗啡在内的阿片类药物不仅通过作用于纹状体中的阿片受体,而且还通过作用于纹状体以外的阿片受体(如在黑质中,也许还通过与阿片受体无关的作用)来影响黑质神经元的活动。

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