Evidence map›Paper›PMID 38748470›Full record

ArticleeLife2024

Comment on 'Accumbens cholinergic interneurons dynamically promote dopamine release and enable motivation'.

James Taniguchi, Riccardo Melani, Lynne Chantranupong, Michelle J Wen, Ali Mohebi, Joshua D Berke, Bernardo L Sabatini, Nicolas X Tritsch

Abstract readComment
In one paragraph

Article in eLife, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing 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

18 citing papers in PubMed.

  1. Article
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  11. Dual cholinergic mechanisms for sculpting striatal dopamine in vivo.bioRxiv : the preprint server for biology · 2025
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  12. Article
  13. Article
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  15. Article
  16. Review
  17. A detailed look at striatal acetylcholine, dopamine, and their interactions.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  18. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors.

James Taniguchi *Neuroscience Institute and Fresco Institute for Parkinson's and Movement Disorders, University Grossman School of Medicine, New York, United States.ORCID 0000-0002-1571-3869
Riccardo Melani *Neuroscience Institute and Fresco Institute for Parkinson's and Movement Disorders, University Grossman School of Medicine, New York, United States.
Lynne ChantranupongDepartment of Neurobiology, Howard Hughes Medical Institute, Harvard Medical School, Boston, United States.ORCID 0000-0001-9814-5264
Michelle J WenDepartment of Neurobiology, Howard Hughes Medical Institute, Harvard Medical School, Boston, United States.
Ali MohebiDepartment of Neurology, University of California, San Francisco, San Francisco, United States.ORCID 0000-0001-7291-3448
Joshua D BerkeDepartment of Neurology, University of California, San Francisco, San Francisco, United States.ORCID 0000-0003-1436-6823
Bernardo L SabatiniDepartment of Neurobiology, Howard Hughes Medical Institute, Harvard Medical School, Boston, United States.ORCID 0000-0003-0095-9177
Nicolas X TritschNeuroscience Institute and Fresco Institute for Parkinson's and Movement Disorders, University Grossman School of Medicine, New York, United States.ORCID 0000-0003-3181-7681

Funding

Dissecting the Synaptic and Cellular Actions of Dopamine in Vivo - Diversity SupplementR01MH130658 · NIMH · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI Tanya Sippy · 2022 to 2026
$3.5M
NIH HHS R01MH130658NIMH NIH HHS R01 MH130658
6 · The paper itself

Abstract

Acetylcholine is widely believed to modulate the release of dopamine in the striatum of mammals. Experiments in brain slices clearly show that synchronous activation of striatal cholinergic interneurons is sufficient to drive dopamine release via axo-axonal stimulation of nicotinic acetylcholine receptors. However, evidence for this mechanism in vivo has been less forthcoming. Mohebi, Collins and Berke recently reported that, in awake behaving rats, optogenetic activation of striatal cholinergic interneurons with blue light readily evokes dopamine release measured with the red fluorescent sensor RdLight1 (Mohebi et al., 2023). Here, we show that blue light alone alters the fluorescent properties of RdLight1 in a manner that may be misconstrued as phasic dopamine release, and that this artefactual photoactivation can account for the effects attributed to cholinergic interneurons. Our findings indicate that measurements of dopamine using the red-shifted fluorescent sensor RdLight1 should be interpreted with caution when combined with optogenetics. In light of this and other publications that did not observe large acetylcholine-evoked dopamine transients in vivo, the conditions under which such release occurs in behaving animals remain unknown.

Indexed as

Cholinergic NeuronsDopamineInterneuronsOptogeneticsAcetylcholineAnimalsMotivationNucleus AccumbensRatsAcetylcholineDopaminebasal gangliadopaminefluorescent probesmouseneuroscienceoptogeneticsphotoactivationphotometry

Identifiers

PMID38748470
PMCPMC11095934

What OpenQuestion holds

Textmetadata
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.