Evidence map›Paper›PMID 36617434›Full record

ArticleThe European journal of neuroscience2023

Characterization of striatal dopamine projections across striatal subregions in behavioral flexibility.

Rochelle K van der Merwe, Jacob A Nadel, Della Copes-Finke, Sean Pawelko, Jesse S Scott, Marwan Ghanem, M Fox, Caroline Morehouse, Robert McLaughlin, Charlie Maddox and 7 more

Abstract read
In one paragraph

Article in The European journal of neuroscience, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Review
  3. Medial septum activation improves strategy switching once strategies are well-learned via bidirectional regulation of dopamine neuron population activity.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2022
    Article
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

17 authors.

Rochelle K van der MerweNeuroscience Department, Oberlin College, Oberlin, Ohio, USA.
Jacob A NadelNeuroscience Department, Oberlin College, Oberlin, Ohio, USA.
Della Copes-FinkeNeuroscience Department, Oberlin College, Oberlin, Ohio, USA.
Sean PawelkoNeuroscience Department, Oberlin College, Oberlin, Ohio, USA.
Jesse S ScottNeuroscience Department, Oberlin College, Oberlin, Ohio, USA.
Marwan GhanemNeuroscience Department, Oberlin College, Oberlin, Ohio, USA.
M FoxNeuroscience Department, Oberlin College, Oberlin, Ohio, USA.
Caroline MorehouseNeuroscience Department, Oberlin College, Oberlin, Ohio, USA.
Robert McLaughlinNeuroscience Department, Oberlin College, Oberlin, Ohio, USA.
Charlie MaddoxNeuroscience Department, Oberlin College, Oberlin, Ohio, USA.
Ruth Albert-LyonsNeuroscience Department, Oberlin College, Oberlin, Ohio, USA.
Golara MalakiNeuroscience Department, Oberlin College, Oberlin, Ohio, USA.
Virginia GroceNeuroscience Department, Oberlin College, Oberlin, Ohio, USA.
Alaina TurocyNeuroscience Department, Oberlin College, Oberlin, Ohio, USA.
Nada AggadiNeuroscience Department, Oberlin College, Oberlin, Ohio, USA.
Xin JinCenter for Motor Control and Disease, Key Laboratory of Brain Functional Genomics, East China Normal University, Shanghai, China.
Christopher D HowardNeuroscience Department, Oberlin College, Oberlin, Ohio, USA.

Funding

Determining the Contribution of Striatal Patches and Dopamine to Habit FormationR15MH122729 · NIMH · OBERLIN COLLEGE · PI HOWARD, CHRISTOPHER D · 2020 to 2020
$396k
NIMH NIH HHS R15 MH122729NIMH NIH HHS R15MH122729-01
6 · The paper itself

Abstract

Behavioural flexibility is key to survival in a dynamic environmentWhile flexible, goal-directed behaviours are initially dependent on dorsomedial striatum, they become dependent on lateral striatum as behaviours become inflexible. Similarly, lesions of dopamine terminals in lateral striatum disrupt the development of inflexible habits. This work suggests that dopamine release in lateral striatum may drive inflexible behaviours, though few studies have investigated a causative role of subpopulations of striatal dopamine terminals in reversal learning, a measure of flexibility. Here, we performed two optogenetic experiments to activate dopamine terminals in dorsomedial (DMS), dorsolateral (DLS) or ventral (nucleus accumbens [NAc]) striatum in DAT-Cre mice that expressed channelrhodopsin-2 via viral injection (Experiment I) or through transgenic breeding with an Ai32 reporter line (Experiment II) to determine how specific dopamine subpopulations impact reversal learning. Mice performed a reversal task in which they self-stimulated DMS, DLS, or NAc dopamine terminals by pressing one of two levers before action-outcome lever contingencies were reversed. Largely consistent with presumed ventromedial/lateral striatal function, we found that mice self-stimulating medial dopamine terminals reversed lever preference following contingency reversal, while mice self-stimulating NAc showed parial flexibility, and DLS self-stimulation resulted in impaired reversal. Impairments in DLS mice were characterized by more regressive errors and reliance on lose-stay strategies following reversal, as well as reduced within-session learning, suggesting reward insensitivity and overreliance on previously learned actions. This study supports a model of striatal function in which DMS and ventral dopamine facilitate goal-directed responding, and DLS dopamine supports more inflexible responding.

Indexed as

Corpus StriatumDopamineAnimalsMiceNeostriatumNucleus AccumbensReversal LearningDopaminebehavioural flexibilitydopamineoptogeneticsreversal learningstriatum

Identifiers

PMID36617434
PMCPMC10329096

What OpenQuestion holds

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Registered trials

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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.