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吗啡而非阿托品可阻断大鼠背侧海马神经元中伤害感受器驱动的活动。

Morphine, but not atropine, blocks nociceptor-driven activity in rat dorsal hippocampal neurones.

作者信息

Sinclair J G, Lo G F

出版信息

Neurosci Lett. 1986 Jul 11;68(1):47-50. doi: 10.1016/0304-3940(86)90227-2.

Abstract

Neurones in the CA1 region of the dorsal hippocampus of urethane-anaesthetized rats were recorded extracellularly with microelectrodes, and tested for their response to non-noxious and noxious peripheral stimuli. None of the cells responded to non-noxious stimuli but 91 of 216 cells were excited by noxious stimuli. Morphine (5.0 mg/kg i.v.) increased the background firing rate in 7 of 10 cells tested and blocked the response to noxious heating of the tail in all cases. Naloxone (0.5 mg/kg i.v.) reversed these effects of morphine. Atropine (0.1 plus 0.2 mg/kg i.v.), in another group of animals, produced only transient changes of an inconsistent nature in 7 cells tested.

摘要

用微电极细胞外记录乌拉坦麻醉大鼠背侧海马CA1区的神经元,并检测它们对无害和有害外周刺激的反应。没有细胞对无害刺激产生反应,但216个细胞中有91个被有害刺激兴奋。吗啡(静脉注射5.0mg/kg)使所测试的10个细胞中的7个细胞的背景放电率增加,并在所有情况下阻断对尾部有害加热的反应。纳洛酮(静脉注射0.5mg/kg)逆转了吗啡的这些作用。在另一组动物中,阿托品(静脉注射0.1加0.2mg/kg)在7个测试细胞中仅产生性质不一致的短暂变化。

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