Fast Spiking Interneurons Autonomously Generate Fast Gamma Oscillations in the Medial Entorhinal Cortex with Excitation Strength Tuning ING–PING Transitions

Gamma oscillations (40-140 Hz) play a fundamental role in neural coordination and cognitive functions in the medial entorhinal cortex (mEC). While previous studies suggest that pyramidal-interneuron network gamma (PING) and interneuron network gamma (ING) mechanisms contribute to these oscillations, the precise role of inhibitory circuits remains unclear. Using optogenetic stimulation and whole-cell electrophysiology in acute mouse brain slices, we examined synaptic input and spike timing in neurons across layer II/III mEC. We found that fast-spiking interneurons exhibited robust gamma-frequency firing, while excitatory neurons engaged in gamma cycle skipping. Stellate and pyramidal cells received minimal recurrent excitation, whereas fast-spiking interneurons received strong excitatory input. Both excitatory neurons and fast-spiking interneurons received gamma-frequency inhibition, emphasizing the role of recurrent inhibition in gamma rhythms. Gamma activity was reduced but persisted after AMPA/kainate receptor blockade, indicating that interneurons can sustain oscillations via an ING mechanism. Selective activation of PV+ interneurons confirmed their ability to sustain fast gamma inhibition autonomously. To further assess the interplay of excitation and inhibition, we developed computational network models constrained by our experimental data. Simulations revealed that weak excitatory input to interneurons supports fast ING-dominated rhythms (∼100-140 Hz) while strengthening excitatory drive induces a transition to slower PING-dominated oscillations (60-100 Hz), although this regime shift was not observed consistently after AMPA/kainate receptor block. These findings highlight the dominant role of inhibitory circuits in sustaining gamma rhythms, demonstrate how excitation strength tunes the oscillatory regime, and refine models of entorhinal gamma oscillations critical for spatial memory processing.

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Journal
eNeuro
Published
2026-01-20
DOI
https://doi.org/10.1523/eneuro.0452-25.2026
Primary Topic
Neural dynamics and brain function
Type
article
Field-Weighted Citation Impact
0.00

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article

Fast Spiking Interneurons Autonomously Generate Fast Gamma Oscillations in the Medial Entorhinal Cortex with Excitation Strength Tuning ING–PING Transitions

Román Baravalle, A. Srinivas, Carmen C. Canavier, Brandon Williams et al.
eNeuro
Neural dynamics and brain function
article

Fast Spiking Interneurons Autonomously Generate Fast Gamma Oscillations in the Medial Entorhinal Cortex with Excitation Strength Tuning ING–PING Transitions

Román Baravalle, A. Srinivas, Carmen C. Canavier, Brandon Williams, Fernando R. Fernandez, John. A. White
article en

Abstract

Gamma oscillations (40-140 Hz) play a fundamental role in neural coordination and cognitive functions in the medial entorhinal cortex (mEC). While previous studies suggest that pyramidal-interneuron network gamma (PING) and interneuron network gamma (ING) mechanisms contribute to these oscillations, the precise role of inhibitory circuits remains unclear. Using optogenetic stimulation and whole-cell electrophysiology in acute mouse brain slices, we examined synaptic input and spike timing in neurons across layer II/III mEC. We found that fast-spiking interneurons exhibited robust gamma-frequency firing, while excitatory neurons engaged in gamma cycle skipping. Stellate and pyramidal cells received minimal recurrent excitation, whereas fast-spiking interneurons received strong excitatory input. Both excitatory neurons and fast-spiking interneurons received gamma-frequency inhibition, emphasizing the role of recurrent inhibition in gamma rhythms. Gamma activity was reduced but persisted after AMPA/kainate receptor blockade, indicating that interneurons can sustain oscillations via an ING mechanism. Selective activation of PV+ interneurons confirmed their ability to sustain fast gamma inhibition autonomously. To further assess the interplay of excitation and inhibition, we developed computational network models constrained by our experimental data. Simulations revealed that weak excitatory input to interneurons supports fast ING-dominated rhythms (∼100-140 Hz) while strengthening excitatory drive induces a transition to slower PING-dominated oscillations (60-100 Hz), although this regime shift was not observed consistently after AMPA/kainate receptor block. These findings highlight the dominant role of inhibitory circuits in sustaining gamma rhythms, demonstrate how excitation strength tunes the oscillatory regime, and refine models of entorhinal gamma oscillations critical for spatial memory processing.

eNeuroVol. 13(2)
Boston University (US), Louisiana State University Health Sciences Center New Orleans (US)
National Science Foundation, National Institutes of Health
Openalex Percentile: Top 84%
Neural dynamics and brain function
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