Suppr超能文献

麻醉性镇痛药及拮抗剂对猫脊髓中对自然刺激产生反应的神经元的作用。

Action of narcotic analgesics and antagonists on spinal units responding to natural stimulation in the cat.

作者信息

Calvillo O, Henry J L, Neuman R S

出版信息

Can J Physiol Pharmacol. 1979 Jun;57(6):652-63. doi: 10.1139/y79-099.

Abstract

Morphine and morphine-related agents were applied by microiontophoresis in the lumbar spinal cord of spinal cats to single units classified on the basis of their responses to natural cutaneous or proprioceptive stimulation. Opiate application had a current-dependent depressant effect on the ongoing activities of about one-third of the units tested. This effect was observed in laminae I and IV--VI, but only with units responding to noxious cutaneous stimuli: the nociceptive responses were themselves depressed. Excitatory and inhibitory responses to glutamate and gamma-aminobutyric acid, respectively, were also depressed. Intravenous administration of the opiates at doses reported to produce analgesia in the cat also depressed only units responding to noxious cutaneous stimuli, including their nociceptive responses. This depression could be reversed by either the iontophoretic application (100 nA) or the intravenous administration (0.1--0.8 mg/kg) of naloxone. These results are interpreted as further evidence that the analgesic effects of opiates are at least partly due to an action at the spinal level.

摘要

在脊髓猫的腰脊髓中,通过微离子透入法将吗啡及与吗啡相关的药物作用于根据对自然皮肤或本体感受刺激的反应分类的单个神经元。阿片类药物的应用对约三分之一受试神经元的持续活动具有电流依赖性抑制作用。这种作用在I层和IV - VI层观察到,但仅在对有害皮肤刺激有反应的神经元中出现:伤害性反应本身受到抑制。对谷氨酸和γ-氨基丁酸的兴奋性和抑制性反应也受到抑制。静脉注射据报道在猫中产生镇痛作用剂量的阿片类药物,同样仅抑制对有害皮肤刺激有反应的神经元,包括它们的伤害性反应。这种抑制作用可通过离子透入法应用(100 nA)或静脉注射(0.1 - 0.8 mg/kg)纳洛酮来逆转。这些结果被解释为进一步证明阿片类药物的镇痛作用至少部分归因于其在脊髓水平的作用。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验