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Comparison of anaesthetic and non-anaesthetic effects on depolarization-evoked glutamate and GABA release from mouse cerebrocortical slices

机译:麻醉剂和非麻醉剂对去极化诱发的谷氨酸和小鼠脑皮质切片中GABA释放的比较

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摘要

Investigation with substances that are similar in structure, but different in anaesthetic properties, may lead to further understanding of the mechanisms of general anaesthesia.We have studied the effects of two cyclobutane derivatives, the anaesthetic, 1-chloro-1,2,2-trifluorocyclobutane (F3), and the non-anaesthetic, 1,2-dichlorohexafluorocyclobutane (F6), on K+-evoked glutamate and γ-aminobutyric acid (GABA) release from isolated, superfused, cerebrocortical slices from mice, by use of h.p.l.c. with fluorescence detection for quantitative analysis.At clinically relevant concentrations, the anaesthetic, F3, inhibited 40 mM K+-evoked glutamate and GABA release by 72% and 47%, respectively, whereas the structurally similar non-anaesthetic, F6, suppressed evoked glutamate release by 70% but had no significant effects on evoked GABA release. A second exposure to 40 mM KCl after a ∼30 min washout of F3 or F6 showed recovery of K+-evoked release, suggesting that F3 and F6 did not cause any non-specific or irreversible changes in the brain slices.Our findings suggest that suppression of excitatory neurotransmitter release may not be directly relevant to the primary action of general anaesthetics. A mechanism involving inhibitory postsynaptic action is implicated, in which a moderate suppression of depolarization-evoked GABA release by the anaesthetic may be consistent with the enhancement of postsynaptic GABAergic activities.
机译:用结构相似但麻醉性质不同的物质进行研究可能会导致人们进一步了解全身麻醉的机理。我们研究了两种环丁烷衍生物麻醉剂1-氯-1,2,2-的作用。三氟环丁烷(F3)和非麻醉剂1,2-二氯六氟环丁烷(F6)通过使用hplc从小鼠分离的,融合的,脑皮质切片中释放出K +诱发的谷氨酸和γ-氨基丁酸(GABA)在临床相关浓度下,麻醉剂F3抑制40 mM K +诱发的谷氨酸和GABA的释放,分别抑制72%和47%,而结构相似的非麻醉剂F6抑制诱发的谷氨酸的释放。降低了70%,但对诱发的GABA释放没有明显影响。 F3或F6洗脱约30分钟后第二次暴露于40 µmM KCl中,表明K +诱发的释放得以恢复,这表明F3和F6不会引起脑切片的任何非特异性或不可逆的变化。兴奋性神经递质的释放可能与全身麻醉剂的主要作用没有直接关系。牵涉一种涉及抑制性突触后作用的机制,其中麻醉剂对去极化诱发的GABA释放的适度抑制可能与增强突触后GABA能活动相一致。

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