Kawato M, Hamaguchi T, Murakami F, Tsukahara N
Biol Cybern. 1984;50(6):447-54. doi: 10.1007/BF00335202.
Several suggestions have been made with regard to the functional significance of dendritic spines in connection with synaptic plasticity. We have shown that for a constant synaptic current, when the synaptic resistance is large compared to the spine-stem resistance, a morphological change in the spine does not produce a marked change in the postsynaptic potential (PSP). When the synaptic resistance is comparable to the spine-stem impedance a morphological change in the spine can induce changes in the synaptic current and the PSP due to the so-called nonlinear effect to the synapse (Kawato and Tsukahara, 1983, 1984). Consequently, in a study of the electrical properties of dendritic spines the input impedance of the parent dendrite, the spinestalk conductance and the conductance change associated with synaptic activity must be considered. We quantitatively estimated all three factors. By comparing electrophysiological data with morphological data, we estimated the synaptic conductance which causes corticorubral EPSP. Its maximum amplitude was 43 nS with a time-to-peak value of 0.3 ms. With this value, the effects of the spine were examined using an improved algorithm based on that of Butz and Cowan (1974). It uses a three-dimensional morphology of the rubrospinal (RS) neurons, which was reconstructed from serial sections containing HRP-filled RS cells. As the spine shortens, the amplitude of the EPSP becomes considerably larger, but its time-to-peak value does not markedly change. Moreover, if unitary EPSP in the RS cell is produced by the activation of several synaptic terminals a morphological change of the spine has a smaller effect on the EPSPs.
关于树突棘在突触可塑性方面的功能意义,已经提出了几种建议。我们已经表明,对于恒定的突触电流,当突触电阻比棘柄电阻大时,棘的形态变化不会在突触后电位(PSP)中产生明显变化。当突触电阻与棘柄阻抗相当时,由于对突触的所谓非线性效应(河本和塚原,1983年,1984年),棘的形态变化可引起突触电流和PSP的变化。因此,在研究树突棘的电特性时,必须考虑母树突的输入阻抗、棘柄电导以及与突触活动相关的电导变化。我们对这三个因素进行了定量估计。通过将电生理数据与形态学数据进行比较,我们估计了引起皮质红核兴奋性突触后电位(EPSP)的突触电导。其最大幅度为43纳西门子,峰值时间为0.3毫秒。利用这个值,使用基于Butz和Cowan(1974年)算法改进的算法来研究棘的效应。它使用了从含有辣根过氧化物酶填充的红核脊髓(RS)细胞的连续切片重建的RS神经元的三维形态。随着棘变短,EPSP的幅度变得相当大,但其峰值时间没有明显变化。此外,如果RS细胞中的单一EPSP是由几个突触终末的激活产生的,那么棘的形态变化对EPSP的影响较小。