Evidence map›Paper›PMID 42182384›Full record

ArticlebioRxiv : the preprint server for biology2026

The Central Nucleus of the Amygdala Encodes the Motivation to Pursue Ethanol.

Matilde Castro, Jingren Gu, Teresa Dong, David J Ottenheimer, Celine Drieu, Patricia H Janak

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2026. 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

6 authors.

Matilde CastroThe Solomon H. Snyder Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, Maryland, 21205.ORCID 0000-0001-7498-483X
Jingren GuThe Solomon H. Snyder Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, Maryland, 21205.
Teresa DongThe Solomon H. Snyder Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, Maryland, 21205.
David J OttenheimerCenter for the Neurobiology of Addiction, Pain, and Emotion, University of Washington, Seattle, Washington, 98195.ORCID 0000-0003-4882-1898
Celine DrieuThe Solomon H. Snyder Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, Maryland, 21205.ORCID 0000-0002-4384-5690
Patricia H JanakThe Solomon H. Snyder Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, Maryland, 21205.ORCID 0000-0002-3333-9049

Funding

Amygdala neural circuits in alcohol intakeR01AA027213 · NIAAA · JOHNS HOPKINS UNIVERSITY · PI JANAK, PATRICIA H. · 2019 to 2023
$2.1M
Role of multi-regional neuronal reactivations in reward-based memoriesR00DA059024 · NIDA · JOHNS HOPKINS UNIVERSITY · PI Celine Drieu · 2026 to 2026
$249k
Role of the central nucleus of the amygdala during ethanol-rewarded instrumental tasksF31AA030921 · NIAAA · JOHNS HOPKINS UNIVERSITY · PI CASTRO, MATILDE · 2023 to 2024
$97k
NIAAA NIH HHS F31 AA030921NIAAA NIH HHS R01 AA027213NIDA NIH HHS R00 DA059024
6 · The paper itself

Abstract

Prior studies implicate the central nucleus of the amygdala (CeA) in reward motivation, yet how this region encodes motivation for ethanol (EtOH) seeking and consumption-and how this compares to encoding of natural rewards-remains poorly understood. We recorded single-unit neural activity from rats during a cued instrumental task in which lever insertion on each trial indicates the opportunity to lever press for ethanol and post-press lever retraction signals ethanol delivery. We found neurons responsive to multiple trial events (lever insertion and retraction cues, lever press, port entry, and reward licks), including neurons with rhythmic activity entrained to licking during EtOH consumption. Notably, CeA neural responses to the lever insertion cue at trial start encoded both the likelihood and speed of engagement during reward seeking. Using a supervised classifier, we found that trial engagement and motivation level could be decoded from pre-trial and lever insertion response periods. Finally, we assessed whether these effects generalized to natural reward seeking. Sucrose-rewarded rats (both ethanol-exposed and ethanol-naïve) showed higher motivation (more rewards earned and shorter first-press latencies) and stronger CeA recruitment and responses at lever insertion than ethanol-rewarded rats, in agreement with the notion that CeA circuits amplify reward-predictive cue signals to facilitate rapid action initiation under high motivational states. Together, these findings indicate that CeA neurons dynamically encode motivational states, with tonic activity and reward-predictive cue responses predicting both engagement in reward seeking and the vigor of action initiation. We suggest these patterns of neural activity drive ethanol and sucrose pursuit.

Identifiers

PMID42182384
PMCPMC13192628

What Socratic holds

Textmetadata
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 Socratic graph.