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首页> 外文期刊>Frontiers in Cellular Neuroscience >N-methyl- D-Aspartate Receptors Contribute to Complex Spike Signaling in Cerebellar Purkinje Cells: An In vivo Study in Mice
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N-methyl- D-Aspartate Receptors Contribute to Complex Spike Signaling in Cerebellar Purkinje Cells: An In vivo Study in Mice

机译: N -甲基- D -天冬氨酸受体促成小脑浦肯野细胞中复杂穗信号的合成:一项体内小鼠研究

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摘要

N -methyl- D -aspartate receptors (NMDARs) are post-synaptically expressed at climbing fiber-Purkinje cell (CF-PC) synapses in cerebellar cortex in adult mice and contributed to CF-PC synaptic transmission under in vitro conditions. In this study, we investigated the role of NMDARs at CF-PC synapses during the spontaneous complex spike (CS) activity in cerebellar cortex in urethane-anesthetized mice, by in vivo whole-cell recording technique and pharmacological methods. Under current-clamp conditions, cerebellar surface application of NMDA (50 μM) induced an increase in the CS-evoked pause of simple spike (SS) firing accompanied with a decrease in the SS firing rate. Under voltage-clamp conditions, application of NMDA enhanced the waveform of CS-evoked inward currents, which expressed increases in the area under curve (AUC) and spikelet number of spontaneous CS. NMDA increased the AUC of spontaneous CS in a concentration-dependent manner. The EC_(50)of NMDA for increasing AUC of spontaneous CS was 33.4 μM. Moreover, NMDA significantly increased the amplitude, half-width and decay time of CS-evoked after-hyperpolarization (AHP) currents. Blockade of NMDARs with D -(-)-2-amino-5-phosphonopentanoic acid ( D -APV, 250 μM) decreased the AUC, spikelet number, and amplitude of AHP currents. In addition, the NMDA-induced enhancement of CS activity could not be observed after α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptors were blocked. The results indicated that NMDARs of CF-PC synapses contributed to the spontaneous CS activity by enhancing CS-evoked inward currents and AHP currents.
机译:N-甲基-D-天冬氨酸受体(NMDARs)在成年小鼠小脑皮层的攀爬纤维-浦肯野细胞(CF-PC)突触中突触后表达,并在体外条件下促进CF-PC突触传递。在这项研究中,我们通过体内全细胞记录技术和药理学方法研究了氨基甲酸乙酯麻醉小鼠小脑皮层自发复杂棘突(CS)活动期间CF-PC突触处NMDAR的作用。在电流钳条件下,小脑表面应用NMDA(50μM)会导致CS诱发的简单尖峰(SS)放电暂停增加,同时SS放电速率降低。在电压钳制条件下,NMDA的施加增强了CS诱发的内向电流的波形,这表示曲线下面积(AUC)和自发CS的小尖峰数增加。 NMDA以浓度依赖的方式增加自发CS的AUC。 NMDA用于增加自发CS的AUC的EC_(50)为33.4μM。此外,NMDA显着增加了CS诱发的超极化后(AHP)电流的幅度,半宽和衰减时间。用D-(-)-2-氨基-5-膦基戊酸(D -APV,250μM)阻断NMDAR会降低AUC,小峰数和AHP电流幅度。另外,在α-氨基-3-羟基-5-甲基-5-异-4-异恶唑丙酸受体被阻断后,NMDA诱导的CS活性增强。结果表明,CF-PC突触的NMDAR通过增强CS诱发的内向电流和AHP电流而促进了自发CS活动。

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