Evidence map›Paper›PMID 41415365›Full record

ArticlebioRxiv : the preprint server for biology2025

Dorsolateral striatal acetylcholine reorganizes neural ensembles to anticipate threat.

Oyku Dinckol, Noah Harris Wenger, Charlie Maddox, Taylor Good, Aryanna Copling, Bhumi Pradipkumar Patel, F Zehra Bozdag, Munir Gunes Kutlu

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Oyku DinckolCenter for Substance Abuse Research (CSAR), Temple University Lewis Katz School of Medicine, Philadelphia, PA, USA.
Noah Harris WengerCenter for Substance Abuse Research (CSAR), Temple University Lewis Katz School of Medicine, Philadelphia, PA, USA.
Charlie MaddoxCenter for Substance Abuse Research (CSAR), Temple University Lewis Katz School of Medicine, Philadelphia, PA, USA.
Taylor GoodDepartment of Cell Biology & Neuroscience, Rowan-Virtua University School of Osteopathic Medicine, Stratford, NJ.
Aryanna CoplingCenter for Substance Abuse Research (CSAR), Temple University Lewis Katz School of Medicine, Philadelphia, PA, USA.
Bhumi Pradipkumar PatelCenter for Substance Abuse Research (CSAR), Temple University Lewis Katz School of Medicine, Philadelphia, PA, USA.
F Zehra BozdagDepartment of Neurosciences, Lerner Research Institute, Cleveland Clinic, Cleveland, OH.
Munir Gunes KutluCenter for Substance Abuse Research (CSAR), Temple University Lewis Katz School of Medicine, Philadelphia, PA, USA.ORCID 0000-0003-2700-977X

Funding

TRAINING PROGRAM: DRUGS OF ABUSE RELATED NEUROPEPTIDEST32DA007237 · NIDA · TEMPLE UNIV OF THE COMMONWEALTH · PI ELLEN M UNTERWALD · 1988 to 2026
$10.6M
Predicting maladaptive aversive learning via computational modeling of insular single cell ensemble activity patternsR21MH132052 · NIMH · VANDERBILT UNIVERSITY · PI KUTLU, MUNIR GUNES · 2023 to 2024
$436k
NIDA NIH HHS T32 DA007237NIMH NIH HHS R21 MH132052
6 · The paper itself

Abstract

Adaptive behavior requires flexible encoding of emotional valence. Although striatal acetylcholine (ACh) signaling is critical for reinforcement learning, its contribution to aversive learning has remained poorly defined. Here, we demonstrate that ACh release in the dorsolateral striatum (DLS) is selectively biased toward negative valence. Using fiber photometry with a genetically encoded ACh sensor, we found that ACh release robustly increased during threat prediction but decreased in anticipation of rewarding outcomes, revealing a bidirectional and valence-specific signature. Optogenetically stimulating ACh release at cue onset accelerated threat learning, impaired extinction, and shifted behavioral responding toward persistent threat expectancy. Concurrent single-cell calcium imaging and optogenetic manipulation revealed that elevated ACh release dynamically reorganized DLS ensemble activity, increasing both excited and inhibited neurons and producing large-scale state-space divergence during threat cues. During extinction, optogenetically sustained ACh release preserved the organization of threat-predictive DLS ensemble activity despite the absence of shock. These findings identify DLS ACh as a valence-specific neuromodulatory signal that reconfigures striatal network dynamics, primes ensembles for impending threat, and biases learning toward threat persistence.

Indexed as

Acetylcholineneural ensemblesStriatumthreat learning

Identifiers

PMID41415365
PMCPMC12710739

What OpenQuestion holds

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LicenceCC BY-ND
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.