Effects of halothane on GABAergic and glutamatergic transmission in isolated hippocampal nerve-synapse preparations

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• 作者：N. Kotani ; M. Wakita ; M.C. Shin ; S. Ogawa ; K. Nonaka ; N. Akaike
• 关键词：Halothane ; Glutamatergic nerve terminal ; Presynaptic GABAA receptor ; Spontaneous and evoked EPSCs ; &lsquo ; Synaptic bouton&rsquo ; preparation
• 刊名：Brain Research
• 出版年：2012
• 出版时间：14 September, 2012
• 年：2012
• 卷：1473
• 期：Complete
• 页码：9-18
• 全文大小：998 K

文摘

We evaluated the effects of halothane on synaptic and extrasynaptic GABA_A and glutamate receptor responses using mechanically dissociated rat hippocampal CA3 neurons in which the well isolated neurons retain functional native nerve endings (the ¡®synaptic bouton¡¯ preparation). The preparation allows the simultaneous comparison of extrasynaptic GABA_A and glutamate receptors, activated by bath applied GABA and glutamate, respectively, to the synaptic receptors measured as spontaneous and evoked postsynaptic currents. Paired-pulse synaptic responses evoked by focal electrical stimulation were also measured to evaluate any presynaptic effects. Halothane enhanced the extrasynaptic GABA_A-receptor mediated postsynaptic responses in a concentration dependent fashion. At clinically relevant concentrations, halothane significantly increased both the amplitude and frequency of spontaneous postsynaptic inhibitory currents (sIPSCs) mediated by synaptic GABA_A receptors. The relative amplitude of evoked IPSCs (eIPSCs) was also increased, concurrent with a decrease in failure rate and a significantly decreased eIPSC paired-pulse ratio. Halothane concentration dependently decreased the extrasynaptic glutamate-receptor induced postsynaptic responses but had no effects on spontaneous or evoked excitatory postsynaptic currents. These results suggest that halothane acts predominantly at presynaptic sites at GABAergic synapses to enhance inhibitory transmission at CA3 synapses, although it also increases extra-synaptic GABA responses. At excitatory synapses on to CA3 neurons, halothane has no presynaptic action¡ªeffecting only extrasynaptic receptors. Our results have clarified the locus of effects of the volatile anesthetic halothane at excitatory and inhibitory synapses, drawing somewhat different conclusions from those deduced from slices and culture systems.