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大鼠海马CA3中间神经元的被动电紧张特性

Passive electrotonic properties of rat hippocampal CA3 interneurones.

作者信息

Chitwood R A, Hubbard A, Jaffe D B

机构信息

Division of Life Sciences, The University of Texas at San Antonio, San Antonio, TX 78249, USA.

出版信息

J Physiol. 1999 Mar 15;515 ( Pt 3)(Pt 3):743-56. doi: 10.1111/j.1469-7793.1999.743ab.x.

Abstract
  1. The linear membrane responses of CA3 interneurones were determined with the use of whole-cell patch recording methods. The mean input resistance (RN) for all cells in this study was 526 +/- 16 MOmega and the slowest membrane time constant (tau0) was 73 +/- 3 ms. 2. The three-dimensional morphology of 63 biocytin-labelled neurones was used to construct compartmental models. Specific membrane resistivity (Rm) and specific membrane capacitance (Cm) were estimated by fitting the linear membrane response. Acceptable fits were obtained for 24 CA3 interneurones. The mean Rm was 61.9 +/- 34.2 Omega cm2 and the mean Cm was 0.9 +/- 0.3 microF cm-2. Intracellular resistance (Ri) could not be resolved in this study. 3. Examination of voltage attenuation revealed a significantly low synaptic efficiency from most dendritic synaptic input locations to the soma. 4. Simulations of excitatory postsynaptic potentials (EPSPs) were analysed at both the site of synaptic input and at the soma. There was little variability in the depolarization at the soma from synaptic inputs placed at different locations along the dendritic tree. The EPSP amplitude at the site of synaptic input was progressively larger with distance from the soma, consistent with a progressive increase in input impedance. 5. The 'iso-efficiency' of spatially different synaptic inputs arose from two opposing factors: an increase in EPSP amplitude at the synapse with distance from the soma was opposed by a nearly equivalent increase in voltage attenuation. These simulations suggest that, in these particular neurones, the amplitude of EPSPs measured at the soma will not be significantly affected by the location of synaptic inputs.
摘要
  1. 使用全细胞膜片钳记录方法测定了CA3中间神经元的线性膜反应。本研究中所有细胞的平均输入电阻(RN)为526±16 MΩ,最慢的膜时间常数(tau0)为73±3 ms。2. 对63个生物素标记神经元的三维形态进行分析,构建了房室模型。通过拟合线性膜反应来估计比膜电阻(Rm)和比膜电容(Cm)。对24个CA3中间神经元获得了可接受的拟合结果。平均Rm为61.9±34.2 Ω·cm2,平均Cm为0.9±0.3 μF·cm-2。本研究中无法解析细胞内电阻(Ri)。3. 对电压衰减的检查显示,从大多数树突突触输入部位到胞体的突触效率显著较低。4. 在突触输入部位和胞体处分析了兴奋性突触后电位(EPSP)的模拟结果。沿着树突树在不同位置放置突触输入时,胞体处的去极化变化很小。突触输入部位的EPSP幅度随着与胞体距离的增加而逐渐增大,这与输入阻抗的逐渐增加一致。5. 空间上不同突触输入的“等效效率”源于两个相反的因素:突触处EPSP幅度随与胞体距离的增加而增大,同时电压衰减也几乎等量增加,二者相互抵消。这些模拟结果表明,在这些特定的神经元中,在胞体处测量的EPSP幅度不会受到突触输入位置的显著影响。

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