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戊巴比妥和氟西泮对未用药猫呼吸神经元的影响。

Effects of pentobarbital and flurazepam on respiratory neurons in undrugged cats.

作者信息

Denavit-Saubié M, Foutz A S, Morin-Surun M P, Boudinot E, Champagnat J, Gonsalves S F

出版信息

Pharmacol Biochem Behav. 1987 Apr;26(4):647-51. doi: 10.1016/0091-3057(87)90591-0.

Abstract

Two hypnotic drugs known to enhance GABAergic transmission, a barbiturate (pentobarbital) and a benzodiazepine (flurazepam), were applied locally to respiratory-related neurons (RN) located in the ventral respiratory area in the medulla of non-anaesthetized cats which were either decerebrated or chronically implanted. Pentobarbital applied iontophoretically depressed the spontaneous discharge rate of most RN tested as well as the increase in firing of RN discharge induced by iontophoretic application of glutamate; pentobarbital also potentiated inhibition induced by iontophoresed GABA. Flurazepam applied by iontophoresis or pressure pulses depressed a minority of RN tested and did not enhance GABA-induced inhibition. These results suggest: that inhibition of RN activity through GABAergic mechanisms can be affected by drugs which act at the chloride ionophore but not those acting indirectly through the benzodiazepine binding site, and the effects of the agents on medullary neuronal activity are independent of an effect on the states of consciousness or on structures rostral to the medulla.

摘要

已知两种增强γ-氨基丁酸(GABA)能传递的催眠药物,一种巴比妥类药物(戊巴比妥)和一种苯二氮䓬类药物(氟西泮),被局部应用于位于未麻醉猫延髓腹侧呼吸区的呼吸相关神经元(RN),这些猫要么已去大脑,要么已长期植入。离子导入法应用戊巴比妥可抑制大多数受试RN的自发放电率,以及离子导入法应用谷氨酸引起的RN放电发放增加;戊巴比妥还增强了离子导入GABA所诱导的抑制作用。通过离子导入法或压力脉冲应用氟西泮可抑制少数受试RN,且不增强GABA诱导的抑制作用。这些结果表明:通过GABA能机制对RN活动的抑制可受作用于氯离子通道的药物影响,但不受通过苯二氮䓬结合位点间接起作用的药物影响,并且这些药物对延髓神经元活动的作用独立于对意识状态或延髓上方结构的影响。

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