Evidence map›Paper›PMID 32269213›Full record

ArticleNature communications2020

Cholinergic midbrain afferents modulate striatal circuits and shape encoding of action strategies.

Daniel Dautan, Icnelia Huerta-Ocampo, Nadine K Gut, Miguel Valencia, Krishnakanth Kondabolu, Yuwoong Kim, Todor V Gerdjikov, Juan Mena-Segovia

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed
5.8field-weighted citation impact, top 3% 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

55 citing papers in PubMed, 89 citations in OpenAlex.

  1. Review
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  5. Striatal cholinergic interneurons exhibit compartment-specific anatomical and functional organization in the mouse.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  6. Article
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  13. A mismatch between striatal cholinergic pauses and dopaminergic reward prediction errors.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  14. The Mesencephalic Locomotor Region: Multiple Cell Types, Multiple Behavioral Roles, and Multiple Implications for Disease.The Neuroscientist : a review journal bringing neurobiology, neurology and psychiatry · 2024
    Review
  15. Article
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  20. A sex-specific effect of MFrontiers in molecular neuroscience · 2024
    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

8 authors at 3 institutions in 4 countries.

Daniel DautanCenter for Molecular and Behavioral Neuroscience, Rutgers University, Newark, NJ, USA. daniel.dautan@iit.it.ORCID http://orcid.org/0000-0003-1001-5727
Icnelia Huerta-OcampoCenter for Molecular and Behavioral Neuroscience, Rutgers University, Newark, NJ, USA.
Nadine K GutCenter for Molecular and Behavioral Neuroscience, Rutgers University, Newark, NJ, USA.
Miguel ValenciaUniversity of Navarra, Neuroscience Program, CIMA, 31008, Pamplona, Spain.ORCID http://orcid.org/0000-0001-5617-5270
Krishnakanth KondaboluCenter for Molecular and Behavioral Neuroscience, Rutgers University, Newark, NJ, USA.
Yuwoong KimCenter for Molecular and Behavioral Neuroscience, Rutgers University, Newark, NJ, USA.
Todor V GerdjikovDepartment of Neuroscience, Physiology and Behavior, University of Leicester, Leicester, LE1 9HN, UK.ORCID http://orcid.org/0000-0002-8889-9182
Juan Mena-SegoviaCenter for Molecular and Behavioral Neuroscience, Rutgers University, Newark, NJ, USA. juan.mena@rutgers.edu.ORCID http://orcid.org/0000-0002-9991-8254
Rutgers, The State University of New Jersey · USNavarre Institute of Health Research · ESUniversity of Leicester · GB

Funding

Cholinergic brainstem signaling in striatal circuitsR01NS100824 · NINDS · RUTGERS THE STATE UNIV OF NJ NEWARK · PI MENA-SEGOVIA, JUAN · 2017 to 2021
$1.7M
NINDS NIH HHS R01 NS100824
6 · The paper itself

Abstract

Assimilation of novel strategies into a consolidated action repertoire is a crucial function for behavioral adaptation and cognitive flexibility. Acetylcholine in the striatum plays a pivotal role in such adaptation, and its release has been causally associated with the activity of cholinergic interneurons. Here we show that the midbrain, a previously unknown source of acetylcholine in the striatum, is a major contributor to cholinergic transmission in the striatal complex. Neurons of the pedunculopontine and laterodorsal tegmental nuclei synapse with striatal cholinergic interneurons and give rise to excitatory responses. Furthermore, they produce uniform inhibition of spiny projection neurons. Inhibition of acetylcholine release from midbrain terminals in the striatum impairs the association of contingencies and the formation of habits in an instrumental task, and mimics the effects observed following inhibition of acetylcholine release from striatal cholinergic interneurons. These results suggest the existence of two hierarchically-organized modes of cholinergic transmission in the striatum, where cholinergic interneurons are modulated by cholinergic neurons of the midbrain.

Indexed as

AnimalsBehavior, AnimalCholinergic NeuronsFemaleGoalsInterneuronsMaleMesencephalonMiceNeostriatumNerve NetNeurons, AfferentOptogeneticsPhosphorylationRats, Long-EvansSynapses

Identifiers

PMID32269213
PMCPMC7142106
OpenAlexW3015370031

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.