Recurrent neural networks with balanced excitation and inhibition exhibit irregular asynchronous dynamics, which is fundamental for cortical computations. Classical balance mechanisms require strong external input currents in order to sustain finite firing rates, thus raising concerns about their biological plausibility. Here, we investigate an alternative mechanism based on short-term synaptic depression (STD) acting on excitatory-excitatory synapses, which dynamically balances the network activity without the need of strong external driving. Using accurate numerical simulations and theoretical investigations we characterize the dynamics of a densely connected recurrent network made up of N rate-neuron models encompassing STD. Depending on the synaptic strength J 0 , the network exhibits two distinct regimes: at sufficiently small J 0 , it converges to a homogeneous fixed point, while for sufficiently large J 0 Rate Chaos emerges. For finite networks, we observe a transition region at intermediate J 0 , where the system passes from the homogeneous fixed point to Rate Chaos following several different routes to chaos depending on the network realization. Furthermore, we show that the width of the transition region shrinks for increasing N and eventually vanishes in the thermodynamic limit ( N → ∞ ). The characterization of the Rate Chaos regime has been performed by means of Dynamical Mean Field (DMF) approaches. This analysis has revealed on one side that the novel balancing mechanism is able to sustain finite irregular activity even in the thermodynamic limit, and on the other side that balancing occurs via dynamic cancellation of the correlations in the synaptic input currents induced by the dense connectivity. Our findings show that STD provides an intrinsic self-regulating mechanism for balanced networks, sustaining irregular yet stable activity without the need of biologically unrealistic strong external currents. This work extends the balanced network paradigm, offering insights into how cortical circuits could maintain robust dynamics via synaptic adaptation.
Angulo‐García et al. (Thu,) studied this question.