A minimal neural circuit model is constructed, in which evidence accumulates in facilitated synaptic efficacy that progressively reshapes the circuit’s phase portrait, eventually driving the network state across the stability boundary and triggering a rapid transition to a choice state.
Abstract
Decision-making requires accumulation of evidence over time, yet exactly how neural circuits implement this computation remains debated. Classical models posit that evidence accumulation is realized by ramping neural activity, whereas recent experimental findings suggest an alternative mechanism in which neural activity remains largely silent before abruptly transitioning into an active decision state. This mechanism leaves a fundamental question unanswered: how is evidence accumulated during the neural activity-silent period? To address this question, we trained excitatory–inhibitory recurrent neural networks (RNNs) with short-term synaptic plasticity (STP) on a reaction-time decision task. We found that after training, the networks learned to leverage STP to make decisions in an activity-silent manner. Choice-tuning analysis revealed a clear functional organization of the network, and connection-pruning analysis uncovered the coupling between choice-selective excitatory and inhibitory neural groups. Guided by the architecture of trained RNNs, we constructed a minimal neural circuit model, in which evidence accumulates in facilitated synaptic efficacy that progressively reshapes the circuit’s phase portrait, eventually driving the network state across the stability boundary and triggering a rapid transition to a choice state. We further compared activity before a choice between the theoretical STP and Static models to examine the potential energy benefit of activity-silent decision-making. Together, our results suggest STP as a mechanism for evidence accumulation in activity-silent decision-making and offer insights into the design of energy-efficient artificial neural networks.
Observations support a view of BTSP as a multi-factor plasticity rule that links synaptic, circuit, and systems-level processes, providing a biologically grounded framework for understanding how the brain rapidly incorporates new information.
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Behavior arises from the interplay between spontaneous brain dynamics and sensory-driven responses, yet how spontaneous neural activity shapes variability in decision-making remains unclear. We leverage the tractable C. elegans nervous system to address this question. During oxygen avoidance, we observe binary trial-to...
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It is suggested that flexible temporal integration can emerge from dynamic interactions between sensory transmission, recurrent decision circuits and temporally structured urgency modulation, providing a mechanistic framework for how neural systems adapt the computation of sensory evidence to changing task demands.
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The Context-modulated Synaptic-states Recurrent Neural Network (CoSyn-RNN), a new continual-learning model inspired by heterogeneous synaptic states and neuro-modulatory control, is introduced, in which protected synaptic states, sparse allocation, and context-dependent modulation support continual learning.
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Behavioral time scale synaptic plasticity (BTSP) allows hippocampal CA1 neurons to form or shift place fields after a single plasticity-inducing plateau potential, but what determines when individual neurons become eligible for another plasticity event remains unclear. Here we propose that recent somatic spike history...
Overall, these results link predictive coding to local circuit plasticity, show it does not require an explicit prediction error representation, and suggest a normative role for BCM-like plasticity in excitatory synapses.
Henrique Reis Aguiar, M. Hennig· bioRxiv· 0 citations
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