Cerebellar circuits anticipate dopamine rewards

Predicting rewards is critical for learning. Although the cerebellum predicts rewards like water and food, it also famously coordinates physical actions like drinking and eating. To disentangle reward prediction from the movements to consume reward, we trained mice to push for delayed dopamine rewards delivered directly into the brain. Via two-photon imaging, we found that many cerebellar granule cells (GrCs) anticipated dopamine with sustained activity that terminated at reward delivery. GrC activity also "stretched" to match 1- or 2-s intervals before dopamine, thereby linking the action to the expected reward time. By contrast, most cerebellar climbing fibers (CFs) spiked just after dopamine delivery. GrC-CF activity also generalized between dopamine versus water rewards, both in individual mice and many individual neurons. Finally, naïve mice 'rewarded' only with CF stimulation also learned to execute a modest number of pushing movements, with similar predictive GrC activity. Thus, cerebellar circuits help animals learn to anticipate rewards even when no consummatory action is needed, suggesting deeper cerebellar integration in brain reward prediction networks.

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Publication Details

Journal
bioRxiv (Cold Spring Harbor Laboratory)
Published
2026-02-03
DOI
https://doi.org/10.64898/2026.02.02.703324
Primary Topic
Vestibular and auditory disorders
Type
article
Field-Weighted Citation Impact
0.00
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article

Cerebellar circuits anticipate dopamine rewards

Amma Otchere, Lizmaylin Ramos, Philipp Maurus, R. B. Ness et al.
bioRxiv (Cold Spring Harbor Laboratory)
Vestibular and auditory disorders
article

Cerebellar circuits anticipate dopamine rewards

Amma Otchere, Lizmaylin Ramos, Philipp Maurus, R. B. Ness, Benjamin Abad Filio, Luke Drake, Subhiksha Srinivasan, Srijan Thota
article en

Abstract

Predicting rewards is critical for learning. Although the cerebellum predicts rewards like water and food, it also famously coordinates physical actions like drinking and eating. To disentangle reward prediction from the movements to consume reward, we trained mice to push for delayed dopamine rewards delivered directly into the brain. Via two-photon imaging, we found that many cerebellar granule cells (GrCs) anticipated dopamine with sustained activity that terminated at reward delivery. GrC activity also "stretched" to match 1- or 2-s intervals before dopamine, thereby linking the action to the expected reward time. By contrast, most cerebellar climbing fibers (CFs) spiked just after dopamine delivery. GrC-CF activity also generalized between dopamine versus water rewards, both in individual mice and many individual neurons. Finally, naïve mice 'rewarded' only with CF stimulation also learned to execute a modest number of pushing movements, with similar predictive GrC activity. Thus, cerebellar circuits help animals learn to anticipate rewards even when no consummatory action is needed, suggesting deeper cerebellar integration in brain reward prediction networks.

bioRxiv (Cold Spring Harbor Laboratory)
National Institutes of Health (US), Brown University (US), National Institute of Neurological Disorders and Stroke (US)
Openalex Percentile: Top 73%
Vestibular and auditory disorders
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