ArticleCerebellum (London, England)2016
Links Between Single-Trial Changes and Learning Rate in Eyelid Conditioning.
Article in Cerebellum (London, England), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 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
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Who cites it
12 citing papers in PubMed.
- Neural circuits encode prior knowledge of temporal statistics.Nature neuroscience · 2026Article
- An emergent temporal basis set robustly supports cerebellar time-series learning.Journal of neurophysiology · 2023Article
- Transitive inference after minimal training in rhesus macaques (Macaca mulatta).Journal of experimental psychology. Animal learning and cognition · 2021Article
- Cannabinoids modulate associative cerebellar learning via alterations in behavioral state.eLife · 2020Article
- Article
- Bidirectional short-term plasticity during single-trial learning of cerebellar-driven eyelid movements in mice.Neurobiology of learning and memory · 2020Article
- Depressed by Learning-Heterogeneity of the Plasticity Rules at Parallel Fiber Synapses onto Purkinje Cells.Cerebellum (London, England) · 2018Review
- Computational Principles of Supervised Learning in the Cerebellum.Annual review of neuroscience · 2018Review
- A cerebellar adaptation to uncertain inputs.Science advances · 2018Article
- Movement Rate Is Encoded and Influenced by Widespread, Coherent Activity of Cerebellar Molecular Layer Interneurons.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2017Article
- Adaptive Acceleration of Visually Evoked Smooth Eye Movements in Mice.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2016Article
- Article
Corrections and comments
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Authors and funding
4 authors.
Funding
Abstract
The discovery of single-trial learning effects, where the presence or absence (or the number) of climbing fiber inputs produces measureable changes in Purkinje cell response and in behavior, represents a major breakthrough in cerebellar learning. Among other things, these observations provide strong links between climbing fiber-mediated plasticity and cerebellar learning. They also demonstrate that cerebellar learning is stochastic, with each instantiation of a movement producing a small increment or decrement in gain. The sum of the small changes give rise to the macroscopic properties of cerebellar learning. We used a relatively large data set from another example of cerebellar-dependent learning, classical conditioning of eyelid responses, to attempt a behavioral replication and extension of single-trial learning effects. As a normal part of training, stimulus-alone trials provide instances where the climbing fiber response would be omitted, similar to non-climbing-fiber trials (gain down) during smooth pursuit training. The consequences of the stimulus-alone trial on the amplitude and timing of the conditioned response on the following paired trials were examined. We find that the amplitude of the conditioned response during the trial after a stimulus-alone trial (no climbing fiber input) was measurably smaller than the amplitude on the previous trials, and this single-trial effect on amplitude is larger for longer interstimulus intervals. The magnitude of the single-trial effect parallels the rate of extinction at different interstimulus intervals supporting the previously observed link between single-trial effects and learning.
Indexed as
Identifiers
26112423What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.