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大鼠海马CA3和CA1锥体神经元中的树突状谷氨酸受体通道。

Dendritic glutamate receptor channels in rat hippocampal CA3 and CA1 pyramidal neurons.

作者信息

Spruston N, 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 Jan 15;482 ( Pt 2)(Pt 2):325-52. doi: 10.1113/jphysiol.1995.sp020521.

Abstract
  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)
摘要
  1. 利用快速施加谷氨酸到从大鼠海马切片中CA3和CA1锥体神经元顶树突分离的外侧膜片上,研究了树突状谷氨酸受体(GluR)通道的特性。CA3膜片在苔藓纤维(MF)突触区域形成(距胞体15 - 76微米),CA1膜片在Schaffer侧支(SC)支配区域形成(距胞体25 - 174微米)。2. 在存在10微摩尔甘氨酸且无细胞外镁离子的情况下,1毫秒的1毫摩尔谷氨酸脉冲引发了双成分反应,包括一个快速上升和衰减的成分,随后是第二个明显更慢的成分。快速成分被2 - 5微摩尔6 - 氰基 - 7 - 硝基喹喔啉 - 2,3 - 二酮(CNQX)选择性阻断,慢速成分被30微摩尔D - 2 - 氨基 - 5 - 膦酰基戊酸(D - AP5)阻断,这表明快速和慢速成分分别由L - α - 氨基 - 3 - 羟基 - 5 - 甲基 - 4 - 异恶唑丙酸(AMPA)型和NMDA型的GluR通道介导。在CA3和CA1树突的膜片中,NMDA与AMPA受体介导成分的峰值幅度比在0.03至0.62之间变化。几乎未观察到缺乏任何一种成分的膜片。3. 快速成分的峰值电流 - 电压(I - V)关系几乎是线性的,而在存在1毫摩尔细胞外镁离子的情况下,慢速成分的I - V关系显示出一个负斜率区域。两种成分的反转电位接近0毫伏。4. 对谷氨酸反应中,偏爱海人酸的GluR通道贡献不大。对1毫摩尔谷氨酸的100毫秒脉冲的反应可被施加1毫摩尔AMPA模拟,而1毫摩尔海人酸产生的电流要小得多,且脱敏作用较弱。这表明快速成分主要由谷氨酸对偏爱AMPA受体的作用介导。5. 通过非平稳波动分析估计,AMPA受体通道的平均单通道电导约为10皮安。这些通道对钙离子的通透性较低(约为对铯离子通透性的5%)。6. NMDA受体通道的单通道电导较大,主要电导状态约为45皮安。这些通道对钙离子的通透性比对铯离子高3.6倍。(摘要截短至400字)
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c0d0/1157732/5f0f609802b0/jphysiol00330-0083-a.jpg

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