Evidence map›Paper›PMID 21704115›Full record

ReviewProgress in neurobiology2011

Molecular substrates of action control in cortico-striatal circuits.

Michael W Shiflett, Bernard W Balleine

Abstract readReview
In one paragraph

Review in Progress in neurobiology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 67 papers.

0numbers the graph read from it
0cells of the map it votes in
67citing papers in PubMed
3.7field-weighted citation impact, top 6% of its field
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

67 citing papers in PubMed, 115 citations in OpenAlex.

  1. Trial
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  7. Enhanced cognitive flexibility and phasic striatal dopamine dynamics in a mouse model of low striatal tonic dopamine.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2024
    Article
  8. Article
  9. Review
  10. Article
  11. Review
  12. Elevated prefrontal dopamine interferes with the stress-buffering properties of behavioral control in female rats.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2023
    Article
  13. Article
  14. Article
  15. Adolescent Dopamine Neurons Represent Reward Differently during Action and State Guided Learning.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2021
    Article
  16. Article
  17. Oxytocin and Addiction: Potential Glutamatergic Mechanisms.International journal of molecular sciences · 2021
    Review
  18. Molecular and circuit mechanisms regulating cocaine memory.Cellular and molecular life sciences : CMLS · 2020
    Review
  19. Review
  20. Neuropilin 2 Signaling Mediates Corticostriatal Transmission, Spine Maintenance, and Goal-Directed Learning in Mice.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2019
    Article

7 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors at 2 institutions in 2 countries.

Michael W ShiflettDepartment of Psychology, Rutgers University, Newark, USA.
Bernard W Balleine
Rutgers, The State University of New Jersey · USUniversity of Sydney · AU

Funding

The Neural Basis of Instrumental ActionR01MH056446 · NIMH · UNIVERSITY OF SYDNEY · PI BALLEINE, BERNARD W · 2003 to 2012
$2.3M
Cortico-Striatal Circuits in Actions and HabitsR01HD059257 · NICHD · UNIVERSITY OF SYDNEY · PI BALLEINE, BERNARD W · 2008 to 2012
$1.0M
Alcohol, Habit and the Failure of Behavioral ControlR01AA018014 · NIAAA · UNIVERSITY OF SYDNEY · PI BALLEINE, BERNARD W · 2008 to 2012
$1.0M
NEURAL BASIS OF INSTRUMENTAL ACTIONR29MH056446 · NIMH · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI BALLEINE, BERNARD W · 1997 to 2001
$198k
NIAAA NIH HHS R01 AA018014NICHD NIH HHS HD59257NICHD NIH HHS R01 HD059257NIMH NIH HHS R01 MH056446NIMH NIH HHS R29 MH056446PHS HHS 29544
6 · The paper itself

Abstract

The purpose of this review is to describe the molecular mechanisms in the striatum that mediate reward-based learning and action control during instrumental conditioning. Experiments assessing the neural bases of instrumental conditioning have uncovered functional circuits in the striatum, including dorsal and ventral striatal sub-regions, involved in action-outcome learning, stimulus-response learning, and the motivational control of action by reward-associated cues. Integration of dopamine (DA) and glutamate neurotransmission within these striatal sub-regions is hypothesized to enable learning and action control through its role in shaping synaptic plasticity and cellular excitability. The extracellular signal regulated kinase (ERK) appears to be particularly important for reward-based learning and action control due to its sensitivity to combined DA and glutamate receptor activation and its involvement in a range of cellular functions. ERK activation in striatal neurons is proposed to have a dual role in both the learning and performance factors that contribute to instrumental conditioning through its regulation of plasticity-related transcription factors and its modulation of intrinsic cellular excitability. Furthermore, perturbation of ERK activation by drugs of abuse may give rise to behavioral disorders such as addiction.

Indexed as

AnimalsCerebral CortexConditioning, ClassicalCorpus StriatumDopamineExtracellular Signal-Regulated MAP KinasesGlutamic AcidHumansLearningNeural PathwaysNeuronal PlasticityRewardDopamineExtracellular Signal-Regulated MAP KinasesGlutamic Acid

Identifiers

PMID21704115
PMCPMC3175490
OpenAlexW2107755617

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

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.