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Estimation of Quantal Size and Number of Functional Active Zones at the Calyx of Held Synapse by Nonstationary EPSC Variance Analysis

机译:非平稳EPSC方差分析估计所持突触花萼的量子大小和功能性活动区的数量

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摘要

At the large excitatory calyx of Held synapse, the quantal size during an evoked EPSC and the number of active zones contributing to transmission are not known. We developed a nonstationary variant of EPSC fluctuation analysis to determine these quantal parameters. AMPA receptor-mediated EPSCs were recorded in slices of young (postnatal 8–10 d) rats after afferent fiber stimulation, delivered in trains to induce synaptic depression. The means and the variances of EPSC amplitudes were calculated across trains for each stimulus number. During 10 Hz trains at 2 mm Ca2+concentration ([Ca2+]), we found linear EPSC variance–mean relationships, with a slope that was in good agreement with the quantal size obtained from amplitude distributions of spontaneous miniature EPSCs. At high release probability with 10 or 15 mm [Ca2+], competitive antagonists were used to partially block EPSCs. Under these conditions, the EPSC variance–mean plots could be fitted with parabolas, giving estimates of quantal size and of the binomial parameter N. With the rapidly dissociating antagonist kynurenic acid, quantal sizes were larger than with a slowly dissociating antagonist, suggesting that the effective glutamate concentration was increased at high release probability. Considering the possibility of multivesicular release and moderate saturation of postsynaptic AMPA receptors, we conclude that the binomial parameter N (637 ± 117; mean ± SEM) represents an upper limit estimate of the number of functional active zones. We estimate that during normal synaptic transmission, the probability of vesicle fusion at single active zones is in the range of 0.25–0.4.
机译:在大的兴奋性突触花萼中,诱发EPSC期间的量子大小和有助于传播的活动区域数量未知。我们开发了EPSC波动分析的非平稳变量来确定这些量化参数。 AMPA受体介导的EPSCs在传入纤维刺激后的幼小(产后8-10 d)大鼠切片中记录,并在火车中传递以诱导突触抑制。针对每个刺激次数,计算出火车之间EPSC振幅的均值和方差。在浓度为2 mm Ca 2 + ([Ca 2 + ])的10 Hz列车中,我们发现线性EPSC方差-均值关系,且斜率吻合良好从自发微型EPSC的振幅分布获得的量子大小。在10或15 mm [Ca 2 + ]的高释放概率下,竞争性拮抗剂被用于部分阻断EPSC。在这种情况下,EPSC方差-均值图可以拟合抛物线,从而给出数量大小和二项式参数N的估计值。对于快速离解的拮抗剂犬尿嘧啶酸,其定量大小要大于缓慢离解的拮抗剂。有效谷氨酸浓度以高释放概率增加。考虑到多泡释放和突触后AMPA受体适度饱和的可能性,我们得出的结论是,二项式参数N(637±117;平均值±SEM)代表功能性活动区数量的上限估计。我们估计,在正常的突触传递过程中,单个活动区的囊泡融合概率为0.25-0.4。

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