ArticleCell reports2026
Cerebellar acceleration of learning in an evidence-accumulation task.
Article in Cell reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
2 citing papers in PubMed.
- Cerebellar-driven cortical dynamics can enable task acquisition, switching and consolidation.Nature communications · 2024Article
- The significance of cerebellar contributions in early-life through aging.Frontiers in computational neuroscience · 2024Article
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Authors and funding
7 authors.
Funding
Abstract
Cerebellar processing contributes to sensory salience, cognition, and behavioral flexibility. Here, we report that learning on a sensory evidence-accumulation task in mice is accelerated by cue-locked optogenetic stimulation of Purkinje cells but not by continuous optogenetic interference. Latent-state analysis revealed that accelerated learning was associated with enhanced focus on current over past trials. A cerebellum-specific transgenic autism model with disrupted Purkinje cell function also unexpectedly showed accelerated learning as well as enhanced reactivity to touch and auditory cues. Transgenic mice and wild-type mice receiving cue-locked stimulation showed prolonged sensory responses in Purkinje cell complex spikes and anterior cingulate cortex, and a subset of Purkinje cells in crus I showed on-task enhanced response to stimuli in wild-type mice. Sensory salience and task state may be different facets of a complex-spike-based mechanism for regulating brain-wide learning mechanisms. These findings potentially link cerebellum-dependent sensory salience with a global weak coherence account of autism.
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Registered trials
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