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吸入麻醉剂在体外对海马体突触反应表现出特定途径和不同的作用。

Inhalation anaesthetics exhibit pathway-specific and differential actions on hippocampal synaptic responses in vitro.

作者信息

MacIver M B, Roth S H

机构信息

Department of Pharmacology & Therapeutics, Faculty of Medicine, University of Calgary, Alberta, Canada.

出版信息

Br J Anaesth. 1988 May;60(6):680-91. doi: 10.1093/bja/60.6.680.

Abstract

The effects of halothane, isoflurane and enflurane were compared on three CNS excitatory synaptic pathways in vitro, to determine whether selective actions described in vivo result from differential effects on anatomically distinct cortical pathways and neurone populations. Halothane (0.25-1.25 vol%) depressed postsynaptic excitability of CA1 pyramidal neurones in response to activation of stratum radiatum synaptic inputs, and concentration-dependent excitatory (0.25-1.25 vol%) and depressant (1.5-2.0 vol%) actions were observed on dentate granule neurone excitability and perforant path evoked synaptic responses. In contrast, isoflurane increased CA1 neurone excitability (0.25-0.75 vol%) and produced postsynaptic depression of dentate neurones (0.5-4.0 vol%). Enflurane also increased CA1 excitability (0.5-4.0 vol%), but depressed synaptic responses at equivalent concentrations, and produced mixed excitatory (0.25-1.0 vol%) and depressant (1.0-4.0 vol%) effects on dentate synaptic responses. Differential actions were also observed for the three anaesthetics on stratum oriens excitatory inputs to CA1 neurones, and on antidromic responses. A good correlation (r = 0.992) exists between the membrane/buffer partition coefficients of these anaesthetics and their half-maximal concentrations for depression of synaptic responses; however, this correlation does not reflect the different, anaesthetic-specific actions observed. The results indicate that inhalation anaesthetics act at multiple and selective hydrophobic recognition sites which are heterogenously distributed on different synaptic pathways.

摘要

在体外比较了氟烷、异氟烷和恩氟烷对三种中枢神经系统兴奋性突触通路的作用,以确定体内描述的选择性作用是否源于对解剖学上不同的皮质通路和神经元群体的不同影响。氟烷(0.25 - 1.25体积%)抑制CA1锥体神经元对放射层突触输入激活的突触后兴奋性,并且在齿状颗粒神经元兴奋性和穿通路径诱发的突触反应上观察到浓度依赖性兴奋作用(0.25 - 1.25体积%)和抑制作用(1.5 - 2.0体积%)。相比之下,异氟烷增加CA1神经元兴奋性(0.25 - 0.75体积%)并导致齿状神经元突触后抑制(0.5 - 4.0体积%)。恩氟烷也增加CA1兴奋性(0.5 - 4.0体积%),但在等效浓度下抑制突触反应,并对齿状突触反应产生混合兴奋作用(0.25 - 1.0体积%)和抑制作用(1.0 - 4.0体积%)。在三种麻醉剂对CA1神经元的原层兴奋性输入以及对逆向反应上也观察到了不同的作用。这些麻醉剂的膜/缓冲液分配系数与其突触反应抑制的半数最大浓度之间存在良好的相关性(r = 0.992);然而,这种相关性并未反映所观察到的不同的、麻醉剂特异性的作用。结果表明,吸入麻醉剂作用于多个选择性疏水识别位点,这些位点在不同的突触通路上呈异质分布。

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