The ASM Journals Committee Values the Contributions of Black Microbiologists.

Abstract

Abstract Oscillations are ubiquitous features of brain dynamics that undergo task-related changes in synchrony, power, and frequency. The impact of those changes on target networks is poorly understood. In this work, we used a biophysically detailed model of prefrontal cortex (PFC) to explore the effects of varying the spike rate, synchrony, and waveform of strong oscillatory inputs on the behavior of cortical networks driven by them. Interacting populations of excitatory and inhibitory neurons with strong feedback inhibition are inhibition-based network oscillators that exhibit resonance (i.e., larger responses to preferred input frequencies). We quantified network responses in terms of mean firing rates and the population frequency of network oscillation; and characterized their behavior in terms of the natural response to asynchronous input and the resonant response to oscillatory inputs. We show that strong feedback inhibition causes the PFC to generate internal (natural) oscillations in the beta/gamma frequency range (>15 Hz) and to maximize principal cell spiking in response to external oscillations at slightly higher frequencies. Importantly, we found that the fastest oscillation frequency that can be relayed by the network maximizes local inhibition and is equal to a frequency even higher than that which maximizes the firing rate of excitatory cells; we call this phenomenon population frequency resonance. This form of resonance is shown to determine the optimal driving frequency for suppressing responses to asynchronous activity. Lastly, we demonstrate that the natural and resonant frequencies can be tuned by changes in neuronal excitability, the duration of feedback inhibition, and dynamic properties of the input. Our results predict that PFC networks are tuned for generating and selectively responding to beta- and gamma-rhythmic signals due to the natural and resonant properties of inhibition-based oscillators. They also suggest strategies for optimizing transcranial stimulation and using oscillatory networks in neuromorphic engineering. Author Summary The prefrontal cortex (PFC) flexibly encodes task-relevant representations and outputs biases to mediate higher cognitive functions. The relevant neural ensembles undergo task-related changes in oscillatory dynamics at beta- and gamma frequencies. Using a computational model of the PFC network, we show that strong feedback inhibition causes the PFC to generate internal oscillations and to prefer external oscillations at similar frequencies. The precise frequencies that are generated and preferred can be flexibly tuned by varying the synchrony and strength of input network activity, the level of background excitation, and neuromodulation of intrinsic ion currents. We also show that the peak output frequency in response to external oscillations, which depends on the synchrony and strength of the input as well as the strong inhibitory feedback, is faster than the internally generated frequency, and that this difference enables exclusive response to oscillatory inputs. These properties enable changes in oscillatory dynamics to govern the selective processing and gating of task-relevant signals in service of cognitive control.