Department of Neuroscience, Physiology and Pharmacology, University College London, London, United Kingdom.
J Neurophysiol. 2013 Jan;109(2):603-20. doi: 10.1152/jn.00528.2012. Epub 2012 Oct 17.
Communication between neurones in the central nervous system depends on synaptic transmission. The efficacy of synapses is determined by pre- and postsynaptic factors that can be characterized using quantal parameters such as the probability of neurotransmitter release, number of release sites, and quantal size. Existing methods of estimating the quantal parameters based on multiple probability fluctuation analysis (MPFA) are limited by their requirement for long recordings to acquire substantial data sets. We therefore devised an algorithm, termed Bayesian Quantal Analysis (BQA), that can yield accurate estimates of the quantal parameters from data sets of as small a size as 60 observations for each of only 2 conditions of release probability. Computer simulations are used to compare its performance in accuracy with that of MPFA, while varying the number of observations and the simulated range in release probability. We challenge BQA with realistic complexities characteristic of complex synapses, such as increases in the intra- or intersite variances, and heterogeneity in release probabilities. Finally, we validate the method using experimental data obtained from electrophysiological recordings to show that the effect of an antagonist on postsynaptic receptors is correctly characterized by BQA by a specific reduction in the estimates of quantal size. Since BQA routinely yields reliable estimates of the quantal parameters from small data sets, it is ideally suited to identify the locus of synaptic plasticity for experiments in which repeated manipulations of the recording environment are unfeasible.
中枢神经系统神经元之间的通讯依赖于突触传递。突触的效能取决于突触前和突触后因素,可以用量子参数来描述,如神经递质释放的概率、释放位点的数量和量子大小。基于多次概率波动分析(MPFA)的现有估计量子参数的方法受到其需要长记录来获取大量数据集的限制。因此,我们设计了一种算法,称为贝叶斯量子分析(BQA),它可以从每次仅 2 种释放概率条件下的 60 次观察中获得小数据集的准确量子参数估计。通过计算机模拟,比较了其在准确性方面与 MPFA 的性能,同时改变了观察次数和模拟释放概率范围。我们用复杂突触的特征复杂性来挑战 BQA,例如增加内部或站点方差,以及释放概率的异质性。最后,我们使用从电生理记录中获得的实验数据验证了该方法,表明 BQA 通过特定减少量子大小的估计值正确地描述了拮抗剂对突触后受体的影响。由于 BQA 可以从小数据集常规地得出可靠的量子参数估计,因此非常适合于识别突触可塑性的位置,对于重复操纵记录环境不可行的实验。