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Thummala, T.

Publications and source records attributed to Thummala, T..

2 recordsLinked to original sources

Impaired representation of temporal statistics in cerebellar degeneration

The nervous system represents the statistical structure of the environment to facilitate perception. In time perception, exploiting prior information through Bayesian inference reduces the influence of perceptual noise. However, the neural substrate underlying this computation remains unknown. The cerebellum is a strong candidate whose integrity is essential for motor and perceptual tasks requiring precise timing, and rodent physiological studies indicate that cerebellar plasticity mechanisms can support the encoding of temporal statistics. To examine how the cerebellum is involved in Bayesian timing, we tested patients with cerebellar degeneration and matched controls on duration reproduction tasks with varying prior distributions. Patients showed the signatures of Bayesian inference, but with greater timing variability, stronger regression toward the mean, and slower updating of the prior. We developed a model of the cerebellar microcircuit in which Purkinje cell plasticity over a granule cell temporal basis set provides a shared substrate for the prior and the inference. Simulations of cerebellar degeneration showed deficits consistent with the behavioral changes observed in the patients. These results suggest a critical role for the human cerebellum in Bayesian inference, with the system generating optimally timed behavior across varying contexts and even remaining robust under extensive neuropathology.

neuroscience↗

Advanced Feedback Enhances Sensorimotor Adaptation

It is widely recognized that sensorimotor learning is enhanced when the feedback is provided throughout the movement compared to when it is provided at the end of the movement. However, the source of this advantage is unclear: Continuous feedback is more ecological, dynamic, and available earlier than endpoint feedback. Here we assess the relative merits of these factors using a method that allows us to manipulate feedback timing independent of actual hand position. By manipulating the onset time of endpoint feedback, we found that adaptation was modulated in a non-monotonic manner, with the peak of the function occurring in advance of the hand reaching the target. Moreover, at this optimal time, learning was of similar magnitude as that observed with continuous feedback. By varying movement duration, we demonstrate that this optimal time occurs at a relatively fixed time after movement onset, an interval we hypothesize corresponds to when the comparison of the sensory prediction and feedback generates the strongest error signal.

neuroscience↗