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Barri, A.

Publications and source records attributed to Barri, A..

3 recordsLinked to original sources

Geometric determinants of time series learning and attractor stability in closed-loop circuits

Skilled volitional behaviours arise from recurrent circuits, which can sustain structured neural activity in the absence of external drive, through internal feedback. But how such autonomous activity is learned and stability maintained in distributed motor circuits is poorly understood. To investigate the relationship between neural representations and learning we compared a cortex-like recurrent neural network (RNN) and a cortico-cerebellar-like circuit with a feed-forward layer (RNN+FFL), both in a closed-loop configuration. RNN+FFL circuits learned periodic target signals that parameter-matched RNNs could not, due to a failure to form attractor states. Decomposing population activity by frequency, rather than variance, separated the task-relevant and task-irrelevant subspaces. Quantifying their geometric arrangement revealed that the feed-forward layer improved learning and stabilised attractor states by increasing the angles within and between these subspaces. Our results show that task-specific representational geometry is a better predictor of periodic time series learning in recurrent circuits than classical global measures such as dimensionality.

neuroscience↗

Synaptic dynamics as a tunable substrate shaping neuronal activity sequences

A central tenet of cerebellar computation posits that granule cells generate sparse spatiotemporal activity patterns that support precisely timed motor and cognitive outputs. Using high-speed in vivo calcium and glutamate imaging combined with slice electrophysiology, we show that heterogeneous synaptic dynamics transform mossy fiber inputs into temporally sparse, sequential patterns of GC activity. Region-specific differences in MF glutamate release shape GC response duration and sparsity, tuning the temporal statistics of population sequences to match sensorimotor associative learning demands. These findings provide direct evidence for temporally sparse GC sequences and establish synaptic dynamics as a ubiquitous, tunable mechanism structuring neural activity in time.

neuroscience↗

Synaptic basis of a sub-second representation of time

Temporal sequences of neural activity are essential for driving well-timed behaviors, but the underlying cellular and circuit mechanisms remain elusive. We leveraged the well-defined architecture of the cerebellum, a brain region known to support temporally precise actions, to explore theoretically whether the experimentally observed diversity of short-term synaptic plasticity (STP) at the input layer could generate neural dynamics sufficient for subsecond temporal learning. Simulated synaptic input generated a diverse set of transient, firing patterns in granule cells (GCs) that provided a temporal basis set for learning precisely timed pauses of Purkinje cell activity associated with delayed eyelid conditioning and Bayesian interval estimation. The learning performance across time intervals was influenced by the temporal bandwidth of the GC basis, which was determined by the input layer synaptic properties. The ubiquity of STP throughout the brain positions it as a general, tunable cellular mechanism for sculpting neural dynamics and fine-tuning behavior.

neuroscience↗