Gustafsson B, McCrea D
J Physiol. 1984 Feb;347:431-51. doi: 10.1113/jphysiol.1984.sp015074.
Shapes of post-synaptic potentials (p.s.p.s) in cat motoneurones were compared with the time course of correlated changes in firing probability during repetitive firing. Excitatory and inhibitory post-synaptic potentials (e.p.s.p.s. and i.p.s.p.s) were evoked by brief triangular stretches of the triceps surae-plantaris muscles. Depolarizing current was injected through the recording micro-electrode to evoke repetitive firing and the post-stimulus time histogram of motoneurone spikes was obtained. E.p.s.p.s (n = 80) of different sizes (30-1040 microV) and rise times (1.1-8.2 ms) were investigated in fifty-nine motoneurones. The majority of the e.p.s.p.s were recorded in triceps surae-plantaris motoneurones with high levels of synaptic noise (estimated peak-to-peak fluctuations of 1.5-3.5 mV). This noise was generated by keeping the triceps surae-plantaris muscles stretched to a near maximal degree. The remaining e.p.s.p.s were recorded in motoneurones to other hind-limb muscles with a low level of synaptic noise. The height of the primary peak of the correlogram with respect to base-line firing rate increased in proportion to both amplitude and rising slope of the e.p.s.p.s. Using normalization procedures or using e.p.s.p.s of constant amplitude but different slopes and vice versa, the relative peak height increased with e.p.s.p. peak derivative with a slope of around 6/mV per millisecond and with e.p.s.p peak amplitude with a slope of about 1/mV. The shape of the correlogram (peak and trough) seemed well described by a linear combination of the shape of the e.p.s.p. derivative and that of the e.p.s.p. itself. The relative e.p.s.p. contribution (e.p.s.p.:e.p.s.p. derivative ratio) varied with e.p.s.p. amplitude and noise level, being largest (mostly 0.25-1.0) for small e.p.s.p.s (100-300 microV) in high levels of synaptic noise and smaller (0-0.25) for larger e.p.s.p.s and for e.p.s.p.s in a low noise background. In conformity with the above finding, a leaky integration of the correlograms gave time courses that in most cases closely resembled the shape of the e.p.s.p.s. The time constant of the leaky circuit (= inverse value of e.p.s.p.:e.p.s.p. derivative ratio) varied with e.p.s.p. amplitude and noise level in the same manner as obtained by direct fitting of e.p.s.p. and e.p.s.p. derivative shape to correlogram shape. Stretch-evoked i.p.s.p.s (n = 10) of small amplitude (90-360 microV as measured close to firing level) were investigated in pre-tibial flexor motoneurones with low levels of synaptic noise. These i.p.s.p.s generated correlogram troughs closely resembling, albeit somewhat wider than, the shape of the i.p.s.p. derivatives.(ABSTRACT TRUNCATED AT 400 WORDS)
将猫运动神经元中突触后电位(p.s.p.s)的形状与重复放电期间放电概率的相关变化时间进程进行了比较。通过对腓肠肌 - 跖肌进行短暂的三角形拉伸来诱发兴奋性和抑制性突触后电位(e.p.s.p.s和i.p.s.p.s)。通过记录微电极注入去极化电流以诱发重复放电,并获得运动神经元动作电位的刺激后时间直方图。在59个运动神经元中研究了不同大小(30 - 1040微伏)和上升时间(1.1 - 8.2毫秒)的兴奋性突触后电位(n = 80)。大多数兴奋性突触后电位记录于具有高水平突触噪声(估计峰 - 峰波动为1.5 - 3.5毫伏)的腓肠肌 - 跖肌运动神经元中。这种噪声是通过将腓肠肌 - 跖肌保持在接近最大程度的拉伸状态而产生的。其余的兴奋性突触后电位记录于支配其他后肢肌肉且突触噪声水平较低的运动神经元中。相对于基线放电率,相关图主峰的高度与兴奋性突触后电位的幅度和上升斜率成比例增加。使用归一化程序或使用恒定幅度但不同斜率的兴奋性突触后电位,反之亦然,相对峰高随兴奋性突触后电位峰导数增加,斜率约为每毫秒6/毫伏,且随兴奋性突触后电位峰幅度增加,斜率约为每毫伏1/毫伏。相关图的形状(峰和谷)似乎可以通过兴奋性突触后电位导数形状和兴奋性突触后电位本身形状的线性组合很好地描述。兴奋性突触后电位的相对贡献(兴奋性突触后电位:兴奋性突触后电位导数比率)随兴奋性突触后电位幅度和噪声水平而变化,对于高水平突触噪声中的小兴奋性突触后电位(100 - 300微伏)最大(大多为0.25 - 1.0),对于较大的兴奋性突触后电位和低噪声背景下的兴奋性突触后电位较小(0 - 0.25)。与上述发现一致,对相关图进行漏积分得到的时间进程在大多数情况下与兴奋性突触后电位的形状非常相似。漏电电路的时间常数(=兴奋性突触后电位:兴奋性突触后电位导数比率的倒数)随兴奋性突触后电位幅度和噪声水平的变化方式与通过将兴奋性突触后电位及其导数形状直接拟合到相关图形状所得到的方式相同。在突触噪声水平较低的胫前屈肌运动神经元中研究了小幅度(在接近放电水平测量为90 - 360微伏)的拉伸诱发抑制性突触后电位(n = 10)。这些抑制性突触后电位产生的相关图谷值与抑制性突触后电位导数的形状非常相似,尽管略宽一些。(摘要截断于400字)