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首页> 外文期刊>The Journal of Physiology >Dendritic glutamate receptor channels in rat hippocampal CA3 and CA1 pyramidal neurons.
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Dendritic glutamate receptor channels in rat hippocampal CA3 and CA1 pyramidal neurons.

机译:大鼠海马CA3和CA1锥体神经元中的树突状谷氨酸受体通道。

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1. Properties of dendritic glutamate receptor (GluR) channels were investigated using fast application of glutamate to outside-out membrane patches isolated from the apical dendrites of CA3 and CA1 pyramidal neurons in rat hippocampal slices. CA3 patches were formed (15-76 microns from the soma) in the region of mossy fibre (MF) synapses, and CA1 patches (25-174 microns from the soma) in the region of Schaffer collateral (SC) innervation. 2. Dual-component responses consisting of a rapidly rising and decaying component followed by a second, substantially slower, component were elicited by 1 ms pulses of 1 mM glutamate in the presence of 10 microM glycine and absence of external Mg2+. The fast component was selectively blocked by 2-5 microM 6-cyano-7-nitroquinoxaline-2,3-dione (CNQX) and the slow component by 30 microM D-2-amino-5-phosphonopentanoic acid (D-AP5), suggesting that the fast and slow components were mediated by the GluR channels of the L-alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionate (AMPA) and NMDA type, respectively. The peak amplitude ratio of the NMDA to AMPA receptor-mediated components varied between 0.03 and 0.62 in patches from both CA3 and CA1 dendrites. Patches lacking either component were rarely observed. 3. The peak current-voltage (I-V) relationship of the fast component was almost linear, whereas the I-V relationship of the slow component showed a region of negative slope in the presence of 1 mM external Mg2+. The reversal potential for both components was close to 0 mV. 4. Kainate-preferring GluR channels did not contribute appreciably to the response to glutamate. The responses to 100 ms pulses of 1 mM glutamate were mimicked by application of 1 mM AMPA, whereas 1 mM kainate produced much smaller, weakly desensitizing currents. This suggests that the fast component is primarily mediated by the action of glutamate on AMPA-preferring receptors. 5. The mean elementary conductance of AMPA receptor channels was about 10 pS, as estimated by non-stationary fluctuation analysis. The permeability of these channels to Ca2+ was low (approximately 5% of the permeability to Cs+). 6. The elementary conductance of NMDA receptor channels was larger, with a main conductance state of about 45 pS. These channels were 3.6 times more permeable to Ca2+ than to Cs+.(ABSTRACT TRUNCATED AT 400 WORDS)
机译:1.通过将谷氨酸快速应用于从大鼠海马切片的CA3和CA1锥体神经元的顶端树突中分离出来的外向外膜片,研究了树突状谷氨酸受体(GluR)通道的特性。在苔藓纤维(MF)突触区域形成CA3斑块(距躯体15-76微米),在Schaffer侧支(SC)神经支配区域形成CA1斑块(距躯体25-174微米)。 2.在存在10 microM甘氨酸和不存在外部Mg2 +的情况下,由1 mM谷氨酸的1 ms脉冲引发由快速上升和下降的组分,然后是第二个基本较慢的组分组成的双组分响应。快速组分被2-5 microM 6-氰基-7-硝基喹喔啉-2,3-二酮(CNQX)选择性阻断,慢组分被30 microM D-2-氨基-5-膦基戊酸(D-AP5)阻断,提示快和慢组分分别由L-α-氨基-3-羟基-5-甲基-4-异恶唑丙酸酯(AMPA)和NMDA型的GluR通道介导。在来自CA3和CA1树突的贴片中,NMDA与AMPA受体介导的组分的峰振幅比在0.03至0.62之间变化。缺少这两种成分的贴剂很少被观察到。 3.快速组分的峰值电流-电压(I-V)关系几乎是线性的,而慢速组分的I-V关系在存在1 mM外部Mg2 +的情况下显示出负斜率区域。两种成分的反向电位都接近0 mV。 4.凯宁酸盐优先的GluR通道对谷氨酸的应答没有明显贡献。通过施加1 mM AMPA可以模拟对100 ms的1 mM谷氨酸脉冲的响应,而1 mM的海藻酸盐产生的电流要小得多,弱化脱敏电流。这表明快速成分主要是由谷氨酸对AMPA优先受体的作用介导的。 5.根据非平稳波动分析估计,AMPA受体通道的平均基本电导约为10 pS。这些通道对Ca2 +的渗透性较低(约占Cs +渗透性的5%)。 6. NMDA受体通道的基本电导较大,主要电导状态约为45 pS。这些通道对Ca2 +的渗透性是对Cs +的3.6倍(抽象截断为400字)

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