Faculty of Health Sciences, Department of Neuroscience and Pharmacology, University of Copenhagen, Denmark.
J Neurophysiol. 2013 Aug;110(4):1021-34. doi: 10.1152/jn.00006.2013. Epub 2013 May 1.
When recording the membrane potential, V, of a neuron it is desirable to be able to extract the synaptic input. Critically, the synaptic input is stochastic and nonreproducible so one is therefore often restricted to single-trial data. Here, we introduce means of estimating the inhibition and excitation and their confidence limits from single sweep trials. The estimates are based on the mean membrane potential, V, and the membrane time constant, τ. The time constant provides the total conductance (G = capacitance/τ) and is extracted from the autocorrelation of V. The synaptic conductances can then be inferred from V when approximating the neuron as a single compartment. We further employ a stochastic model to establish limits of confidence. The method is verified on models and experimental data, where the synaptic input is manipulated pharmacologically or estimated by an alternative method. The method gives best results if the synaptic input is large compared with other conductances, the intrinsic conductances have little or no time dependence or are comparably small, the ligand-gated kinetics is faster than the membrane time constant, and the majority of synaptic contacts are electrotonically close to soma (recording site). Although our data are in current clamp, the method also works in V-clamp recordings, with some minor adaptations. All custom made procedures are provided in Matlab.
在记录神经元的膜电位(V)时,理想情况下能够提取出突触输入。至关重要的是,突触输入是随机且不可重复的,因此通常只能使用单次试验数据。在这里,我们引入了从单次扫掠试验中估计抑制和兴奋及其置信限的方法。这些估计基于平均膜电位(V)和膜时间常数(τ)。时间常数提供了总电导(G=电容/τ),并从 V 的自相关中提取出来。当将神经元近似为单个隔室时,可以从 V 中推断出突触电导。我们进一步采用随机模型来建立置信限。该方法在模型和实验数据上得到了验证,其中通过药理学操纵或通过替代方法来估计突触输入。如果与其他电导相比,突触输入较大,内在电导的时间依赖性较小或比较小,配体门控动力学比膜时间常数快,并且大多数突触接触在电紧张(记录部位)上接近胞体,则该方法效果最佳。虽然我们的数据是在电流钳位下获得的,但该方法在 V 钳位记录中也适用,只需进行一些微小的调整。所有定制的程序都在 Matlab 中提供。