Evidence map›Paper›PMID 37272423›Full record

ArticleeLife2023

Accumbens cholinergic interneurons dynamically promote dopamine release and enable motivation.

Ali Mohebi, Val L Collins, Joshua D Berke

Open access · goldAbstract read
In one paragraph

Article in eLife, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed, 1 pooled it
11.7field-weighted citation impact, top 1% 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

47 citing papers in PubMed, 1 synthesis or guideline pooled it, 76 citations in OpenAlex.

  1. Pooled it
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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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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors at 1 institution in 1 country.

Ali MohebiDepartment of Neurology, University of California, San Francisco, San Francisco, United States.ORCID 0000-0001-7291-3448
Val L CollinsDepartment of Neurology, University of California, San Francisco, San Francisco, United States.
Joshua D BerkeDepartment of Neurology, University of California, San Francisco, San Francisco, United States.ORCID 0000-0003-1436-6823
University of California, San Francisco · US

Funding

Dopaminergic mechanisms for motivation and reinforcement learningR01DA045783 · NIDA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI JOSHUA D BERKE · 2018 to 2026
$4.1M
Neural mechanisms linking need to rewardRF1NS116626 · NINDS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI BERKE, JOSHUA D, KNIGHT, ZACHARY A. · 2020 to 2020
$2.7M
Striatal Microcircuit DynamicsR01NS123516 · NINDS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI BERKE, JOSHUA D · 2021 to 2025
$2.1M
Neural mechanisms linking need to rewardR01NS116626 · NINDS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI BERKE, JOSHUA D, KNIGHT, ZACHARY A. · 2023 to 2024
$1.7M
Dopaminergic modulation of prefrontal cortex during working memoryK01MH126223 · NIMH · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI MOHEBI, ALI · 2021 to 2023
$575k
Encoding and regulation of compulsion-like alcohol drinking by subtypes of nucleus accumbens core neuronsR21AA027157 · NIAAA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI BERKE, JOSHUA D, HOPF, FREDERIC WOODWARD · 2018 to 2019
$421k
NIAAA NIH HHS R21 AA027157NIDA NIH HHS R01 DA045783NIMH NIH HHS K01 MH126223NINDS NIH HHS R01 NS116626NINDS NIH HHS R01 NS123516NINDS NIH HHS RF1 NS116626
6 · The paper itself

Abstract

Motivation to work for potential rewards is critically dependent on dopamine (DA) in the nucleus accumbens (NAc). DA release from NAc axons can be controlled by at least two distinct mechanisms: (1) action potentials propagating from DA cell bodies in the ventral tegmental area (VTA), and (2) activation of β2* nicotinic receptors by local cholinergic interneurons (CINs). How CIN activity contributes to NAc DA dynamics in behaving animals is not well understood. We monitored DA release in the NAc Core of awake, unrestrained rats using the DA sensor RdLight1, while simultaneously monitoring or manipulating CIN activity at the same location. CIN stimulation rapidly evoked DA release, and in contrast to slice preparations, this DA release showed no indication of short-term depression or receptor desensitization. The sound of unexpected food delivery evoked a brief joint increase in CIN population activity and DA release, with a second joint increase as rats approached the food. In an operant task, we observed fast ramps in CIN activity during approach behaviors, either to start the trial or to collect rewards. These CIN ramps co-occurred with DA release ramps, without corresponding changes in the firing of lateral VTA DA neurons. Finally, we examined the effects of blocking CIN influence over DA release through local NAc infusion of DHβE, a selective antagonist of β2* nicotinic receptors. DHβE dose-dependently interfered with motivated approach decisions, mimicking the effects of a DA antagonist. Our results support a key influence of CINs over motivated behavior via the local regulation of DA release.

Indexed as

DopamineReceptors, NicotinicAnimalsCholinergic AgentsInterneuronsMotivationRatsVentral Tegmental AreaCholinergic AgentsDopamineReceptors, Nicotinicacetylcholineapproachdopaminemotivationneuroscienceratstriatum

Identifiers

PMID37272423
PMCPMC10259987
OpenAlexW4379377046

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.