Evidence map›Paper›PMID 40338017›Full record

ArticleeLife2025

Dynamics of striatal action selection and reinforcement learning.

Jack W Lindsey, Jeffrey Markowitz, Winthrop F Gillis, Sandeep R Datta, Ashok Litwin-Kumar

Abstract read
In one paragraph

Article in eLife, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Reward-driven adaptation of movements requires strong recurrent basal ganglia-cortical loops.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  4. Article
  5. Article
  6. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors.

Jack W LindseyKavli Institute for Brain Science, Columbia University, New York, United States.ORCID https://orcid.org/0000-0003-0930-7327
Jeffrey MarkowitzWallace H. Coulter Department of Biomedical Engineering, Georgia Institute of Technology and Emory University, Atlanta, United States.ORCID https://orcid.org/0000-0003-2362-1937
Winthrop F GillisDepartment of Neurobiology, Harvard Medical School, Boston, United States.
Sandeep R DattaDepartment of Neurobiology, Harvard Medical School, Boston, United States.
Ashok Litwin-KumarKavli Institute for Brain Science, Columbia University, New York, United States.ORCID https://orcid.org/0000-0003-2422-6576

Funding

Motion Sequencing for All: Pipelining, Distribution and Training to Enable Broad Adoption of a Next-Generation Platform for Behavioral and Neurobehavioral AnalysisU24NS109520 · NINDS · HARVARD MEDICAL SCHOOL · PI DATTA, SANDEEP R · 2019 to 2024
$2.3M
CounterAct Administrative Supplement to NS114020 Automated Phenotyping in EpilepsyR01NS114020 · NINDS · STANFORD UNIVERSITY · PI DATTA, SANDEEP R, SOLTESZ, IVAN · 2019 to 2023
$2.3M
Neurobehavioral phenotyping of AD model mice using Motion SequencingRF1AG073625 · NIA · HARVARD MEDICAL SCHOOL · PI DATTA, SANDEEP R · 2021 to 2021
$1.9M
Burroughs Wellcome Fund Career Award at the Scientific InterfaceNIA NIH HHS RF1 AG073625NIH HHS R01NS114020NIH HHS RF1AG073625NIH HHS U24NS109520NINDS NIH HHS R01 NS114020NINDS NIH HHS U24 NS109520
6 · The paper itself

Abstract

Spiny projection neurons (SPNs) in dorsal striatum are often proposed as a locus of reinforcement learning in the basal ganglia. Here, we identify and resolve a fundamental inconsistency between striatal reinforcement learning models and known SPN synaptic plasticity rules. Direct-pathway (dSPN) and indirect-pathway (iSPN) neurons, which promote and suppress actions, respectively, exhibit synaptic plasticity that reinforces activity associated with elevated or suppressed dopamine release. We show that iSPN plasticity prevents successful learning, as it reinforces activity patterns associated with negative outcomes. However, this pathological behavior is reversed if functionally opponent dSPNs and iSPNs, which promote and suppress the current behavior, are simultaneously activated by efferent input following action selection. This prediction is supported by striatal recordings and contrasts with prior models of SPN representations. In our model, learning and action selection signals can be multiplexed without interference, enabling learning algorithms beyond those of standard temporal difference models.

Indexed as

Corpus StriatumLearningNeuronsReinforcement, PsychologyAnimalsMiceModels, NeurologicalNeuronal Plasticitybasal ganglianeurosciencenonereinforcement learningsynaptic plasticity

Identifiers

PMID40338017
PMCPMC12061475

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

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.