Goal-driven optimization of single-neuron properties in artificial networks reveals regularization role of neural diversity and adaptation in the brain

Abstract

AbstractNeurons in the brain have rich and adaptive input-output properties. Features such as diverse f-I curves and spike frequency adaptation are known to place single neurons in optimal coding regimes when facing changing stimuli. Yet, it is still unclear how brain circuits exploit single neuron flexibility, and how network-level requirements may have shaped such cellular function. To answer this question, a multi-scaled approach is needed where the computations of single neurons and of neural circuits must be considered as a complete system. In this work, we use artificial neural networks to systematically investigate single neuron input-output adaptive mechanisms, optimized in an end-to-end fashion. Throughout the optimization process, each neuron has the liberty to modify its nonlinear activation function, parametrized to mimic f-I curves of biological neurons, and to learn adaptation strategies to modify activation functions in real-time during a task. We find that such networks show much-improved robustness to noise and changes in input statistics. Importantly, we find that this procedure recovers precise coding strategies found in biological neurons, such as gain scaling and fractional order differentiation/integration. Using tools from dynamical systems theory, we analyze the role of these emergent single neuron properties and argue that neural diversity and adaptation plays an active regularization role that enables neural circuits to optimally propagate information across time.