Hanse E, Gustafsson B
Institute of Physiology and Pharmacology, Goteborg University, Sweden.
J Physiol. 2001 Mar 1;531(Pt 2):481-93. doi: 10.1111/j.1469-7793.2001.0481i.x.
Factors determining the release probability were examined using whole-cell patch-clamp recording and minimal stimulation (10 impulses, 50 Hz) of individual glutamatergic synapses, containing single release sites, on pyramidal neurones in the CA1 region of hippocampal slices from neonatal rats. Release probability following the first action potential in the burst (P1) varied among the synapses from 0 to 0.87 (mean +/- s.d.; 0.35 +/- 0.28, n = 52) and the average release during the burst (burst pool) varied from 0.4 to 4.1 events (1.7 +/- 0.85, n = 52). Heterogeneity in P1 did not co-vary with that of the burst pool. By selecting burst trials during which only one release event occurred, the vesicle release probability (Pves) at a release site could be determined. It was found to vary considerably among the synapses, from 0.04 to 0.94 (0.43 +/- 0.28, n = 43). This heterogeneity correlated significantly with that of P1 such that more than half of the variation of P1 could be explained by a variation in Pves. The average number of vesicles directly available for release at the onset of the burst (the pre-primed pool) was estimated as the cumulative release up to that point in the burst where a second release event did not produce higher initial release probability than that found in trials where only one vesicle was released. The average pre-primed pool varied among the synapses from 0.4 to 2.1 (1.03 +/- 0.42, n = 43). It co-varied significantly with that of P1 such that it could explain the remaining variation in P1. The difference between the burst pool and the pre-primed pool suggests the presence of a fast (< 100 ms), activity-dependent priming of vesicles. Some synapses (9/52) did not show any initial release (P1 = 0), but release occurred later during the burst ('low frequency mute synapses'). Their behaviour was explained by an absence of a pre-primed pool.
采用全细胞膜片钳记录和对新生大鼠海马切片CA1区锥体神经元上含单个释放位点的单个谷氨酸能突触进行最小刺激(10个脉冲,50Hz),研究了决定释放概率的因素。爆发中第一个动作电位后的释放概率(P1)在突触间变化范围为0至0.87(均值±标准差;0.35±0.28,n = 52),爆发期间的平均释放量(爆发池)变化范围为0.4至4.1次事件(1.7±0.85,n = 52)。P1的异质性与爆发池的异质性并不共同变化。通过选择仅发生一次释放事件的爆发试验,可以确定释放位点的囊泡释放概率(Pves)。发现其在突触间差异很大,范围为0.04至0.94(0.43±0.28,n = 43)。这种异质性与P1的异质性显著相关,以至于P1超过一半的变化可以由Pves的变化来解释。爆发开始时可直接用于释放的囊泡平均数量(预引发池)估计为爆发中到第二个释放事件不会产生比仅释放一个囊泡的试验中更高的初始释放概率的那个点的累积释放量。平均预引发池在突触间变化范围为0.4至2.1(1.03±0.42,n = 43)。它与P1的异质性显著共同变化,以至于可以解释P1中剩余的变化。爆发池和预引发池之间的差异表明存在快速(<100ms)的、活动依赖性的囊泡引发。一些突触(9/52)没有显示任何初始释放(P1 = 0),但在爆发后期发生了释放(“低频沉默突触”)。它们的行为可以通过不存在预引发池来解释。