The Hamiltonian brain: efficient probabilistic inference with excitatory-inhibitory neural circuit dynamics

TL;DR

This paper shows that cortical neural dynamics, including oscillations and transients, can be explained as features of Hamiltonian Monte Carlo inference in excitatory-inhibitory circuits, improving computational efficiency.

Contribution

It introduces a model linking HMC inference with excitatory-inhibitory neural dynamics, explaining oscillations and transients as functional features for efficient probabilistic inference.

Findings

Oscillations speed up inference by rapidly exploring state space.

Model reproduces stimulus-dependent oscillation frequency and transients.

Inhibition lags excitation, matching observed neural dynamics.

Abstract

Probabilistic inference offers a principled framework for understanding both behaviour and cortical computation. However, two basic and ubiquitous properties of cortical responses seem difficult to reconcile with probabilistic inference: neural activity displays prominent oscillations in response to constant input, and large transient changes in response to stimulus onset. Here we show that these dynamical behaviours may in fact be understood as hallmarks of the specific representation and algorithm that the cortex employs to perform probabilistic inference. We demonstrate that a particular family of probabilistic inference algorithms, Hamiltonian Monte Carlo (HMC), naturally maps onto the dynamics of excitatory-inhibitory neural networks. Specifically, we constructed a model of an excitatory-inhibitory circuit in primary visual cortex that performed HMC inference, and thus inherently gave rise to oscillations and transients. These oscillations were not mere epiphenomena but served an important functional role: speeding up inference by rapidly spanning a large volume of state space. Inference thus became an order of magnitude more efficient than in a non-oscillatory variant of the model. In addition, the network matched two specific properties of observed neural dynamics that would otherwise be difficult to account for in the context of probabilistic inference. First, the frequency of oscillations as well as the magnitude of transients increased with the contrast of the image stimulus. Second, excitation and inhibition were balanced, and inhibition lagged excitation. These results suggest a new functional role for the separation of cortical populations into excitatory and inhibitory neurons, and for the neural oscillations that emerge in such excitatory-inhibitory networks: enhancing the efficiency of cortical computations.