TY - JOUR
T1 - Synaptic inhibition and excitation estimated via the time constant of membrane potential fluctuations
AU - Berg, Rune W.
AU - Ditlevsen, Susanne
PY - 2013/5/8
Y1 - 2013/5/8
N2 - 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, V̄, 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 V̄ 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.
AB - 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, V̄, 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 V̄ 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.
U2 - 10.1152/jn.00006.2013
DO - 10.1152/jn.00006.2013
M3 - Journal article
C2 - 23636725
SN - 0022-3077
VL - 110
SP - 1021
EP - 1034
JO - Journal of Neurophysiology
JF - Journal of Neurophysiology
IS - 4
ER -