Winegar Bruce D, MacIver M Bruce
Neuroscience Program, Department of Anesthesia, Stanford University School of Medicine, Stanford, CA 94305-5117, USA.
BMC Neurosci. 2006 Jan 12;7:5. doi: 10.1186/1471-2202-7-5.
Anesthetic-induced CNS depression is thought to involve reduction of glutamate release from nerve terminals. Recent studies suggest that isoflurane reduces glutamate release by block of Na channels. To further investigate this question we examined the actions of isoflurane, TTX, extracellular Ca2+, CNQX and stimulus voltage (stim) on glutamate-mediated transmission at hippocampal excitatory synapses. EPSPs were recorded from CA1 neurons in rat hippocampal brain slices in response to Schaffer-collateral fiber stimulation.
Isoflurane (350 microM; 1 MAC) reversibly depressed EPSP amplitudes by ~60% while facilitation increased approximately 20%. Consistent with previous studies, these results indicate a presynaptic site of action that involves reduced excitation-release coupling. EPSPs were depressed to comparable levels by TTX (60 nM) or lowered stim, but facilitation was not changed, indicating a simple failure of axonal conduction. Similarly, partial antagonism of postsynaptic glutamate receptors with CNQX (10 microM) depressed EPSP amplitudes with no change in facilitation. However, EPSP depression by low external Ca2+ (0.8 mM) was accompanied by an increase in facilitation comparable to isoflurane. Isoflurane depression of EPSP amplitudes could also be partly reversed by high external Ca2+ (4 mM) that also decreased facilitation. Isoflurane or low Ca2+ markedly reduced the slopes of fiber volley (FV)-EPSP input-output curves, consistent with little or no effect on FVs. By contrast, TTX didn't alter the FV-EPSP curve slope, indicating that EPSP depression resulted from FV depression. FVs were remarkably resistant to isoflurane. Somatic spike currents were unaffected by 350 microM (1 MAC) isoflurane as well. The EC50 for isoflurane depression of FVs was approximately 2.8 mM (12 vol. %; 8 MAC).
Isoflurane appears to depress CA1 synapses at presynaptic sites downstream from Na channels, as evident by the increased facilitation that accompanies EPSP depression. Fiber volleys did not exhibit depression by isoflurane, as has been reported for other brain regions.
麻醉诱导的中枢神经系统抑制被认为与神经末梢谷氨酸释放减少有关。最近的研究表明,异氟烷通过阻断钠通道来减少谷氨酸释放。为了进一步研究这个问题,我们检测了异氟烷、河豚毒素(TTX)、细胞外钙离子、CNQX和刺激电压对海马兴奋性突触处谷氨酸介导的传递的作用。在大鼠海马脑片中,记录CA1神经元对Schaffer侧支纤维刺激产生的兴奋性突触后电位(EPSP)。
异氟烷(350微摩尔;1个最低肺泡有效浓度)使EPSP幅度可逆性降低约60%,同时易化作用增加约20%。与先前的研究一致,这些结果表明其作用位点在突触前,涉及兴奋-释放偶联的减弱。TTX(60纳摩尔)或降低刺激电压可使EPSP降低到类似水平,但易化作用未改变,这表明只是轴突传导失败。同样,用CNQX(10微摩尔)对突触后谷氨酸受体进行部分拮抗可降低EPSP幅度,而对易化作用无影响。然而,低细胞外钙离子(0.8毫摩尔)引起的EPSP降低伴随着易化作用的增加,与异氟烷作用类似。高细胞外钙离子(4毫摩尔)可部分逆转异氟烷引起的EPSP幅度降低,同时也降低了易化作用。异氟烷或低钙离子显著降低纤维群峰电位(FV)-EPSP输入-输出曲线的斜率,这与对FV几乎没有影响一致。相比之下,TTX未改变FV-EPSP曲线斜率,表明EPSP降低是由FV降低导致的。FV对异氟烷具有显著抗性。350微摩尔(1个最低肺泡有效浓度)的异氟烷对体细胞动作电位电流也无影响。异氟烷抑制FV的半数有效浓度(EC50)约为2.8毫摩尔(12体积%;8个最低肺泡有效浓度)。
异氟烷似乎在钠通道下游的突触前位点抑制CA1突触,这可从EPSP降低伴随易化作用增加看出。如在其他脑区所报道的那样,纤维群峰电位未表现出被异氟烷抑制。