Motoneurons can count: A cell intrinsic spike number memory compensates for deviations from rate coding

Abstract

Firing rate is an important means of encoding information in many types of neurons. A prime example is asynchronous flight as used by [~]600,000 insect species (Dudley, 2018), where wingbeat frequency and flight power output are controlled by a rate code of the flight power motoneurons (Hurkey et al., 2023). The five motoneurons that innervate the wing depressor muscle fibers translate different magnitudes of excitatory drive smoothly into changes of their common firing rates, which in turn, are linearly related to wing power output (Gordon and Dickinson, 2006). Such motoneuron input/output properties are called type-I excitability and are achieved by the expression of specific combinations of ion currents that linearize the frequency-input current curve. But are there additional motoneuron properties that compensate for acute perturbation of their rate code? Here we combine in vivo electrophysiology with Drosophila genetics to test for mechanisms that compensate for transient perturbation of rate coding during behavior. We show that MN intrinsic properties compensate for the occurrence of extra spikes by delaying the subsequent spikes, thus restoring rate coding fidelity. The underlying mechanism is dose and phase dependent. First, compensatory increases of subsequent interspike interval durations grow with the number of supernumerous spikes that interfere with coding. Second, the magnitude of the compensation for single extra spikes depends on when during an interspike interval these occur. This mechanism depends at least in part on axonally localized HCN channels and increases the fidelity of motoneuron rate coding in the light of perturbation during flight motor behavior.