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吗啡和甲硫氨酸脑啡肽酰胺对胶状质和背角深层中伤害感受器驱动神经元的作用。

Actions of morphine and met-enkephalin-amide on nociceptor driven neurones in substantia gelatinosa and deeper dorsal horn.

作者信息

Sastry B R, Goh J W

出版信息

Neuropharmacology. 1983 Jan;22(1):119-22. doi: 10.1016/0028-3908(83)90270-8.

Abstract

Simultaneous recordings of responses of substantia gelatinosa and deep dorsal horn neurones to thermal noxious cutaneous stimulation were made in spinalized cats anaesthetized with urethane/chloralose. Morphine, whether applied iontophoretically in the substantia gelatinosa (50-200 nA) or injected intravenously (1.0-1.5 mg/kg), enhanced the responses of the substantia gelatinosa cells while depressing those of deep cells. Met-enkephalin-amide (50-200 nA) also had similar reciprocal actions. Naloxone counteracted these effects of the agonists. The results support our previous proposal that the opiates facilitate the activity of a substantia gelatinosa system that controls the responses of deep dorsal horn neurones to pain.

摘要

在用乌拉坦/氯醛糖麻醉的脊髓猫中,同时记录了脊髓背角胶状质和深层神经元对热伤害性皮肤刺激的反应。吗啡,无论是通过离子导入法施用于脊髓背角胶状质(50 - 200 nA)还是静脉注射(1.0 - 1.5 mg/kg),都会增强脊髓背角胶状质细胞的反应,同时抑制深层细胞的反应。甲硫氨酸脑啡肽酰胺(50 - 200 nA)也有类似的相反作用。纳洛酮可抵消激动剂的这些作用。这些结果支持了我们之前的观点,即阿片类药物促进了一个控制脊髓背角深层神经元对疼痛反应的脊髓背角胶状质系统的活动。

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