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大鼠海马齿状回篮状细胞中钙离子通透的AMPA和NMDA受体通道

Ca(2+)-permeable AMPA and NMDA receptor channels in basket cells of rat hippocampal dentate gyrus.

作者信息

Koh D S, Geiger J R, Jonas P, Sakmann B

机构信息

Max-Planck-Institut für medizinische Forschung, Abteilung Zellphysiologie, Heidelberg, Germany.

出版信息

J Physiol. 1995 Jun 1;485 ( Pt 2)(Pt 2):383-402. doi: 10.1113/jphysiol.1995.sp020737.

Abstract
  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 isolation in 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)
摘要
  1. 在大鼠海马切片齿状回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、树突形态以及在持续电流注入期间产生动作电位的高频特性来识别。2. 通过将谷氨酸快速施加到从篮状细胞胞体分离的外向膜片(10微摩尔甘氨酸,无细胞外镁离子)上,激活了双成分电流。快速成分被6-氰基-7-硝基喹喔啉-2,3-二酮(CNQX)选择性阻断,慢速成分被D-2-氨基-5-膦酰基戊酸(D-AP5)阻断。这表明这两个成分分别由α-氨基-3-羟基-5-甲基-4-异恶唑丙酸受体(AMPAR)/海人酸受体和N-甲基-D-天冬氨酸受体(NMDAR)通道介导。NMDAR成分的峰值电流与AMPAR/海人酸受体成分的峰值电流的平均比值为0.22(10毫摩尔谷氨酸的1毫秒脉冲)。3. 在D-AP5存在下单独研究的AMPAR/海人酸受体成分,基于与海人酸相比AMPA的优先激活、海人酸激活电流的弱脱敏、AMPA和海人酸之间的交叉脱敏以及环噻嗪对脱敏的减少,被鉴定为AMPAR介导。4. 在1毫秒谷氨酸脉冲后,篮状细胞AMPAR的失活时间常数(τ)为1.2±0.1毫秒(平均值±标准误)。在100毫秒谷氨酸脉冲期间,AMPAR以3.7±0.2毫秒的τ脱敏。5. 在富含钠离子的细胞外溶液中,AMPAR介导电流的峰值电流-电压(I-V)关系显示反转电位为-4.0±2.6毫伏,其特征为双整流形状。使用非平稳波动分析估计单个AMPAR通道的电导为22.6±1.6皮秒。海马篮状细胞中表达的AMPAR具有高度的钙离子通透性(PCa/PK = 1.79)。6. 在CNQX存在下单独研究海马篮状细胞中的NMDAR。由谷氨酸脉冲激活的NMDAR的失活呈双指数形式,平均τ值分别为266±23毫秒(76%)和2620±383毫秒(24%)。7. 在富含钠离子的细胞外溶液中,NMDAR介导成分的峰值I-V关系显示反转电位为1.5±0.6毫伏,并且在存在细胞外镁离子的情况下,在负膜电位处有一个负斜率区域,这是由于这些离子的电压依赖性阻断。主要开放状态下单个NMDAR通道的电导为50.2±1.8皮秒。(摘要截取自400字)

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