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首页> 外文期刊>The Journal of Physiology >Ca(2+)-permeable AMPA and NMDA receptor channels in basket cells of rat hippocampal dentate gyrus.
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Ca(2+)-permeable AMPA and NMDA receptor channels in basket cells of rat hippocampal dentate gyrus.

机译:Ca(2+)渗透大鼠海马齿状回的篮子细胞中的AMPA和NMDA受体通道。

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1. Glutamate receptor (GluR) channels were studied in basket cells in the dentate gyrus of rat hippocampal slices. Basket cells were identified by their location, dendritic morphology and high frequency of action potentials generated during sustained current injection. 2. Dual-component currents were activated by fast application of glutamate to outside-out membrane patches isolated from basket cell somata (10 microM glycine, no external Mg2+). The fast component was selectively blocked by 6-cyano-7-nitroquinoxaline-2,3-dione (CNQX), the slow component by D-2-amino-5-phosphonopentanoic acid (D-AP5). This suggests that the two components were mediated by alpha-amino-3- hydroxy-5-methyl-4-isoxazolepropionate receptor (AMPAR)/kainate receptor and N-methyl-D-aspartate receptor (NMDAR) channels, respectively. The mean ratio of the peak current of the NMDAR component to that of the AMPAR/kainate receptor component was 0.22 (1 ms pulses of 10 mM glutamate). 3. The AMPAR/kainate receptor component, which was studied in isolation in the presence of D-AP5, was identified as AMPAR mediated on the basis of the preferential activation by AMPA as compared with kainate, the weak desensitization of kainate-activated currents, the cross-desensitization between AMPA and kainate, and the reduction of desensitization by cyclothiazide. 4. Deactivation of basket cell AMPARs following 1 ms pulses of glutamate occurred with a time constant (tau) of 1.2 +/- 0.1 ms (mean +/- S.E.M.). During 100 ms glutamate pulses AMPARs desensitized with a tau of 3.7 +/- 0.2ms. 5. The peak current-voltage (I-V) relation of AMPAR-mediated currents in Na(+)-rich extracellular solution showed a reversal potential of -4.0 +/- 2.6 mV and was characterized by a a doubly rectifying shape. The conductance of single AMPAR channels was estimated as 22.6 +/- 1.6 pS using non-stationary fluctuation analysis. AMPARs expressed in hippocampal basket cells were highly Ca2+ permeable (PCa/PK = 1.79). 6. NMDARs in hippocampal basket cells were studied in isolationin the presence of CNQX. Deactivation of NMDARs activated by glutamate pulses occurred bi-exponentially with mean tau values of 266 +/- 23 ms (76%) and 2620 +/- 383 ms (24%). 7. The peak I-V relation of the NMDAR-mediated component in Na(+)-rich extracellular solution showed a reversal potential of 1.5 +/- 0.6 mV and a region of negative slope at negative membrane potentials in the presence of external Mg2+, due to voltage-dependent block by these ions. The conductance of single NMDAR channels in the main open state was 50.2 +/- 1.8 pS.(ABSTRACT TRUNCATED AT 400 WORDS)
机译:1.在大鼠海马切片的齿状回中的篮状细胞中研究了谷氨酸受体(GluR)通道。篮状细胞通过其位置,树突形态和持续电流注入期间产生的动作电位的高频率来鉴定。 2.通过将谷氨酸快速应用到从篮细胞体细胞分离的外而外膜片(10 microM甘氨酸,无外部Mg2 +)上激活双组分电流。快速组分被6-氰基-7-硝基喹喔啉-2,3-二酮(CNQX)选择性阻断,慢组分被D-2-氨基-5-膦基戊酸(D-AP5)阻断。这表明这两个组分分别由α-氨基-3-羟基-5-羟基-5-甲基-4-异恶唑丙酸酯受体(AMPAR)/海藻酸酯受体和N-甲基-D-天冬氨酸受体(NMDAR)通道介导。 NMDAR组件的峰值电流与AMPAR /海因酸酯受体组件的峰值电流的平均比值为0.22(10 ms谷氨酸的1 ms脉冲)。 3.在D-AP5存在下单独研究的AMPAR /海藻酸酯受体组分,被确定为AMPAR介导的AMPAR介导的AMPAR介导的作用,与海藻酸盐相比,海藻酸酯活化的电流弱脱敏, AMPA和海藻酸盐之间的交叉脱敏作用,以及环噻嗪减少脱敏作用。 4.在1ms的谷氨酸脉冲后,使篮式细胞AMPAR失活,其时间常数(tau)为1.2 +/- 0.1ms(平均+/- S.E.M。)。在100毫秒的谷氨酸脉冲期间,AMPA以3.7 +/- 0.2毫秒的tau脱敏。 5.在富含Na(+)的细胞外溶液中AMPAR介导的电流的峰值电流-电压(I-V)关系显示出-4.0 +/- 2.6 mV的反向电势,并具有双整流形状。使用非平稳波动分析,单个AMPAR通道的电导估计为22.6 +/- 1.6 pS。在海马篮子细胞中表达的AMPAR具有高Ca2 +渗透性(PCa / PK = 1.79)。 6.在存在CNQX的情况下,对海马篮细胞中的NMDAR进行了分离研究。谷氨酸脉冲激活的NMDAR失活呈双指数发生,平均tau值为266 +/- 23 ms(76%)和2620 +/- 383 ms(24%)。 7.在富含Na(+)的细胞外溶液中NMDAR介导的组分的IV峰关系显示,在存在外部Mg2 +的情况下,反向电位为1.5 +/- 0.6 mV,在负膜电位处存在负斜率区域。这些离子对电压依赖性的阻挡。在主打开状态下单个NMDAR通道的电导为50.2 +/- 1.8 pS。(抽象截断为400字)

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