Evidence map›Paper›PMID 41870239›Full record

ArticleeLife2026

Alcohol attenuates CRF-induced excitatory effects from the extended amygdala to dorsostriatal cholinergic interneurons.

Amanda Essoh, Xueyi Xie, Himanshu Gangal, Zhenbo Huang, Ruifeng Chen, Ziyi Li, Xuehua Wang, Valerie Vierkant, Miguel A Garza, Lierni Ugartemendia and 5 more

Abstract read
In one paragraph

Article in eLife, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Alcohol and Opioids Modulate Excitatory Inputs to the SCN.bioRxiv : the preprint server for biology · 2026
    Article
  5. Article
  6. Article
  7. Article
  8. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors.

Amanda Essoh *Department of Neuroscience and Experimental Therapeutics, College of Medicine, Texas A&M University Health Science Center, Bryan, United States.ORCID https://orcid.org/0000-0002-7899-5920
Xueyi Xie *Department of Neuroscience and Experimental Therapeutics, College of Medicine, Texas A&M University Health Science Center, Bryan, United States.ORCID https://orcid.org/0000-0002-2349-1223
Himanshu GangalDepartment of Neuroscience and Experimental Therapeutics, College of Medicine, Texas A&M University Health Science Center, Bryan, United States.ORCID https://orcid.org/0000-0002-6901-3067
Zhenbo HuangDepartment of Neuroscience and Experimental Therapeutics, College of Medicine, Texas A&M University Health Science Center, Bryan, United States.ORCID https://orcid.org/0000-0003-4857-5500
Ruifeng ChenDepartment of Neuroscience and Experimental Therapeutics, College of Medicine, Texas A&M University Health Science Center, Bryan, United States.ORCID https://orcid.org/0009-0007-4650-959X
Ziyi LiDepartment of Neuroscience and Experimental Therapeutics, College of Medicine, Texas A&M University Health Science Center, Bryan, United States.ORCID https://orcid.org/0009-0006-6611-669X
Xuehua WangDepartment of Neuroscience and Experimental Therapeutics, College of Medicine, Texas A&M University Health Science Center, Bryan, United States.ORCID https://orcid.org/0009-0003-6887-7968
Valerie VierkantDepartment of Neuroscience and Experimental Therapeutics, College of Medicine, Texas A&M University Health Science Center, Bryan, United States.ORCID https://orcid.org/0000-0001-7457-497X
Miguel A GarzaDepartment of Neuroscience and Experimental Therapeutics, College of Medicine, Texas A&M University Health Science Center, Bryan, United States.ORCID https://orcid.org/0009-0007-2079-8231
Lierni UgartemendiaCenter for Metabolic and Degenerative Disease, Institute of Molecular Medicine, University of Texas, Houston, United States.ORCID https://orcid.org/0000-0001-6423-0188
Maria E SecciDepartment of Physiology, Louisiana State University Health Sciences Center, New Orleans, United States.ORCID https://orcid.org/0000-0001-5769-1250
Nicholas W GilpinDepartment of Physiology, Louisiana State University Health Sciences Center, New Orleans, United States.ORCID https://orcid.org/0000-0001-8901-8917
Nicholas J JusticeCenter for Metabolic and Degenerative Disease, Institute of Molecular Medicine, University of Texas, Houston, United States.ORCID https://orcid.org/0000-0002-4673-390X
Robert O MessingDepartment of Neuroscience, University of Texas, Austin, United States.ORCID https://orcid.org/0000-0002-5345-4431
Jun WangDepartment of Neuroscience and Experimental Therapeutics, College of Medicine, Texas A&M University Health Science Center, Bryan, United States.ORCID https://orcid.org/0000-0002-0085-4722

Funding

Transformation of the stress response into motor behavior by the external globus pallidusR01MH112768 · NIMH · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI JUSTICE, NICHOLAS J · 2017 to 2021
$2.3M
Ethanol drinking and the basal ganglia circuitryR01AA027768 · NIAAA · TEXAS A&M UNIVERSITY HEALTH SCIENCE CTR · PI WANG, JUN · 2020 to 2024
$2.0M
Striatal ensemble plasticity in alcohol use disorderR01AA030293 · NIAAA · TEXAS A&M UNIVERSITY HEALTH SCIENCE CTR · PI Jun Wang · 2023 to 2026
$1.8M
CRF neurons of the extended amygdala and alcohol drinkingR01AA026075 · NIAAA · UNIVERSITY OF TEXAS AT AUSTIN · PI MESSING, ROBERT O. · 2017 to 2021
$1.7M
Synaptic Plasticity and Alcohol Use DisorderU01AA025932 · NIAAA · TEXAS A&M UNIVERSITY HEALTH SCIENCE CTR · PI WANG, JUN · 2017 to 2021
$1.6M
Ethanol and glutamatergic transmission in the dorsal striatumR01AA021505 · NIAAA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI WANG, JUN · 2012 to 2016
$1.4M
Direct activation of CRF neurons by Abeta disrupts the stress response in Alzheimer's DiseaseR21AG086907 · NIA · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI JUSTICE, NICHOLAS J · 2024 to 2024
$429k
NIAAA NIH HHS R01AA021505NIAAA NIH HHS R01AA026075NIAAA NIH HHS R01AA027768NIAAA NIH HHS R01AA030293NIAAA NIH HHS U01AA025932NIMH NIH HHS R01MH112768NIMH NIH HHS R21AG086907
6 · The paper itself

Abstract

Alcohol relapse is associated with corticotropin-releasing factor (CRF) signaling and altered reward pathway function, though the precise mechanisms remain unclear. Here, using both mice and rats, we investigated how CRF modulates cholinergic interneurons (CINs) in the dorsal striatum, a region critical in mediating cognitive flexibility and action selection. Using monosynaptic and retrograde circuit tracing, we identified direct inputs from CRF-expressing (CRF

Indexed as

AmygdalaCholinergic NeuronsCorpus StriatumCorticotropin-Releasing HormoneEthanolInterneuronsAcetylcholineAnimalsCRF Receptor, Type 1MaleMiceMice, Inbred C57BLRatsReceptors, Corticotropin-Releasing HormoneAcetylcholineCorticotropin-Releasing HormoneCRF Receptor, Type 1EthanolReceptors, Corticotropin-Releasing HormoneacetylcholinealcoholBNSTCeAcholinergic interneuronCRFdorsal striatummouseneurosciencerat

Identifiers

PMID41870239
PMCPMC13008356

What OpenQuestion holds

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Registered trials

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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.