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Saponati, M.

Publications and source records attributed to Saponati, M..

3 recordsLinked to original sources

Inhibitory feedback enables predictive learning of multiple sequences in neural networks

Anticipating future events is a key computational task for neuronal networks. Experimental evidence suggests that reliable temporal sequences in neural activity play a functional role in the association and anticipation of events in time. However, how neurons can differentiate and anticipate multiple spike sequences remains largely unknown. We implement a learning rule based on predictive processing, where neurons exclusively fire for the initial, unpredictable inputs in a spiking sequence, leading to an efficient representation with reduced post-synaptic firing. Combining this mechanism with inhibitory feedback leads to sparse firing in the network, enabling neurons to selectively anticipate different sequences in the input. We demonstrate that intermediate levels of inhibition are optimal to decorrelate neuronal activity and to enable the prediction of future inputs. Notably, each sequence is independently encoded in the sparse, anticipatory firing of the network. Overall, our results demonstrate that the interplay of self-supervised predictive learning rules and inhibitory feedback enables fast and efficient classification of different input sequences.

neuroscience↗

Sequence anticipation and STDP emerge from a voltage-based predictive learning rule

Intelligent behavior depends on the brains ability to anticipate future events. However, the learning rules that enable neurons to predict and fire ahead of sensory inputs remain largely unknown. We propose a plasticity rule based on predictive processing, where the neuron learns a low-rank model of the synaptic input dynamics in its membrane potential. Neurons thereby amplify those synapses that maximally predict other synaptic inputs based on their temporal relations, which provide a solution to an optimization problem that can be implemented at the single-neuron level using only local information. Consequently, neurons learn sequences over long timescales and shift their spikes towards the first inputs in a sequence. We show that this mechanism can explain the development of anticipatory signalling and recall in a recurrent network. Furthermore, we demonstrate that the learning rule gives rise to several experimentally observed STDP (spike-timing-dependent plasticity) mechanisms. These findings suggest prediction as a guiding principle to orchestrate learning and synaptic plasticity in single neurons.

neuroscience↗

Thalamocortical spectral transmission relies on balanced input strengths

The thalamus is a key element of sensory transmission in the brain, as all sensory information is processed by the thalamus before reaching the cortex. The thalamus is known to gate and select sensory streams through a modulation of its internal activity in which spindle oscillations play a preponderant role, but the mechanism underlying this process is not completely understood. In particular, how do thalamocortical connections convey stimulus-driven information selectively over the background of thalamic internally generated activity (such as spindle oscillations)? Here we investigate this issue with a spiking network model of connectivity between thalamus and primary sensory cortex reproducing the local field potential of both areas. We found two features of the thalamocortical dynamics that filter out spindle oscillations: i) spindle oscillations are weaker in neurons projecting to the cortex, ii) the resonance dynamics of cortical networks selectively blocks frequency in the range encompassing spindle oscillations. This latter mechanism depends on the balance of the strength of thalamocortical connections toward excitatory and inhibitory neurons in the cortex. Our results pave the way toward an integrated understanding of the sensory streams traveling between the periphery and the cortex.

neuroscience↗