Lin J W, Faber D S
Department of Physiology, State University of New York, Buffalo 14214.
J Neurosci. 1988 Apr;8(4):1302-12. doi: 10.1523/JNEUROSCI.08-04-01302.1988.
Simultaneous pre- and postsynaptic intracellular recordings, combined with HRP injections, were used to study the properties of junctional transmission between club endings of saccular nerve afferents and the Mauthner (M-) cell in goldfish. All endings were electrotonically coupled to the M-cell, but impulses in less than 20% of the afferents produced chemically mediated excitatory postsynaptic potentials as well. There were no differences between the coupling potentials of those endings that mediated chemical transmission and those that did not, and presynaptic injections of HRP confirmed that in both cases the studied fibers terminated on the M-cell as single club endings. Since electron microscopic studies (Nakajima, 1974; Kohno and Noguchi, 1986; Tuttle et al., 1986) have consistently revealed structural correlates of chemical synapses in all the endings, we propose that the chemical synapses in the majority of the club endings are functionally silent. The electrotonic coupling at these junctions was characterized on the basis of coupling coefficients and DC transfer resistances. Coupling coefficients for anti- and orthodromic action potentials averaged 0.076 and 0.011, respectively. The transfer resistances measured with injections of constant-current pulses were the same in both directions (approximately 18.6 k omega), indicating the junctions do not rectify. Two separate calculations of the gap junctional resistance indicated that it is in the range of 6.7-35.8 M omega, with a mean value of 15.5 M omega. This calculated junctional resistance corresponds to 670 open gap junction channels, assuming a single-channel conductance of 100 pS. As that estimate is about 2 orders of magnitude smaller than the number of the presumed morphological correlates of the channels, i.e., intramembranous particles observed with the technique of freeze-fracture (Kohno and Noguchi, 1986; Tuttle et al., 1986), we conclude that only a small fraction of the morphologically observed channels are open at any time. The characteristics of the chemically mediated EPSPs were as follows: amplitude, 0.139 +/- 0.075 mV (mean +/- SD; n = 16); latency from onset of the coupling potential, 636 +/- 26 mu sec (n = 24); 10-90% rise time, 244 +/- 33 mu sec (n = 14); and decay time constant, 1.32 +/- 0.51 msec (n = 6). The decay phase was fit by a single exponential, and its time constant presumably is the same as that of the underlying conductance change since the M-cell's membrane time constant is significantly faster, 0.3-0.4 msec.
同时进行突触前和突触后细胞内记录,并结合辣根过氧化物酶(HRP)注射,用于研究金鱼球囊神经传入纤维的终末与莫氏(M-)细胞之间的突触传递特性。所有终末均与M细胞发生电突触耦合,但不到20%的传入纤维冲动也能产生化学介导的兴奋性突触后电位。介导化学传递的终末与未介导化学传递的终末之间的耦合电位没有差异,突触前注射HRP证实,在这两种情况下,所研究的纤维均以单个终末终止于M细胞上。由于电子显微镜研究(中岛,1974;小野和野口,1986;塔特尔等人,1986)一直揭示所有终末中化学突触的结构相关性,我们提出大多数球囊终末中的化学突触在功能上是沉默的。这些连接处的电突触耦合通过耦合系数和直流传递电阻进行表征。逆向和正向动作电位的耦合系数平均分别为0.076和0.011。通过注入恒流脉冲测量的双向传递电阻相同(约18.6 kΩ),表明这些连接处不发生整流。对缝隙连接电阻的两种独立计算表明,其范围在6.7 - 35.8 MΩ之间,平均值为15.5 MΩ。假设单通道电导为100 pS,该计算出的连接电阻对应于670个开放的缝隙连接通道。由于该估计值比推测的通道形态学相关物数量小约2个数量级,即通过冷冻断裂技术观察到的膜内颗粒数量(小野和野口,1986;塔特尔等人,1986),我们得出结论,在任何时候,形态学上观察到的通道中只有一小部分是开放的。化学介导的兴奋性突触后电位的特征如下:幅度,0.139±0.075 mV(平均值±标准差;n = 16);从耦合电位开始的潜伏期,636±26 μs(n = 24);10 - 90%上升时间,244±33 μs(n = 14);以及衰减时间常数,1.32±0.51 ms(n = 6)。衰减相符合单指数函数,其时间常数可能与潜在的电导变化时间常数相同,因为M细胞的膜时间常数明显更快,为0.3 - 0.4 ms。