Abstract

A balance between excitatory and inhibitory synaptic currents is thought to be important for several aspects of information processing in cortical neurons in vivo, including gain control, bandwidth and receptive field structure. These factors will affect the firing rate of cortical neurons and their reliability, with consequences for their information coding and energy consumption. Yet how balanced synaptic currents contribute to the coding efficiency and energy efficiency of cortical neurons remains unclear. We used single compartment computational models with stochastic voltage-gated ion channels to determine whether synaptic regimes that produce balanced excitatory and inhibitory currents have specific advantages over other input regimes. Specifically, we compared models with only excitatory synaptic inputs to those with equal excitatory and inhibitory conductances, and stronger inhibitory than excitatory conductances (i.e. approximately balanced synaptic currents). Using these models, we show that balanced synaptic currents evoke fewer spikes per second than excitatory inputs alone or equal excitatory and inhibitory conductances. However, spikes evoked by balanced synaptic inputs are more informative (bits/spike), so that spike trains evoked by all three regimes have similar information rates (bits/s). Consequently, because spikes dominate the energy consumption of our computational models, approximately balanced synaptic currents are also more energy efficient than other synaptic regimes. Thus, by producing fewer, more informative spikes approximately balanced synaptic currents in cortical neurons can promote both coding efficiency and energy efficiency.

Highlights

  • Cortical neurons receive many thousands of weak excitatory synaptic inputs [1], the majority of which originate from other local or distant neurons within the cortex [2,3]

  • We have shown that approximately balanced inhibitory and excitatory synaptic currents increase both coding efficiency and energy efficiency in comparison to two other synaptic input regimes – excitation alone, and balanced excitatory and inhibitory conductances

  • The strong inhibitory conductance needed to generate a current that balances the excitatory current produced the lowest spike rates of all the regimes we studied across the entire input stimulus space

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Summary

Introduction

Cortical neurons receive many thousands of weak (sub-millivolt) excitatory synaptic inputs [1], the majority of which originate from other local or distant neurons within the cortex [2,3]. During ongoing activity in vivo, excitatory and inhibitory currents depolarize the membrane from the resting potential to around 260 mV, slightly below the threshold for spike initiation [7]. For excitatory and inhibitory currents to balance at approximately 260 mV, the inhibitory conductances must be larger than excitatory conductances. Operating this close to threshold, small fluctuations in synaptic inputs can depolarize the neuron sufficiently to trigger spikes, giving rise to highly variable interspike intervals, similar to those expected from a Poisson process [4,5]. Depolarization by balanced excitatory and inhibitory currents affects numerous aspects of information processing in cortical neurons

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