Evidence map›Paper›PMID 38509197›Full record

ArticleMolecular psychiatry2024

Chemogenetic inhibition of central amygdala CRF-expressing neurons decreases alcohol intake but not trauma-related behaviors in a rat model of post-traumatic stress and alcohol use disorder.

Bryan Cruz, Valentina Vozella, Vittoria Borgonetti, Ryan Bullard, Paula C Bianchi, Dean Kirson, Luisa B Bertotto, Michal Bajo, Roman Vlkolinsky, Robert O Messing and 2 more

Abstract read
In one paragraph

Article in Molecular psychiatry, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Central amygdalaNeurobiology of stress · 2026
    Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
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

12 authors.

Bryan CruzDepartment of Molecular Medicine, The Scripps Research Institute, La Jolla, CA, 92073, USA.ORCID 0000-0002-7418-1524
Valentina VozellaDepartment of Molecular Medicine, The Scripps Research Institute, La Jolla, CA, 92073, USA.
Vittoria BorgonettiDepartment of Molecular Medicine, The Scripps Research Institute, La Jolla, CA, 92073, USA.
Ryan BullardDepartment of Molecular Medicine, The Scripps Research Institute, La Jolla, CA, 92073, USA.
Paula C BianchiDepartment of Molecular Medicine, The Scripps Research Institute, La Jolla, CA, 92073, USA.
Dean KirsonDepartment of Pharmacology, Addiction Science, and Toxicology, The University of Tennessee Health Science Center, Memphis, TN, 38163, USA.
Luisa B BertottoDepartment of Molecular Medicine, The Scripps Research Institute, La Jolla, CA, 92073, USA.ORCID 0000-0002-5457-4208
Michal BajoDepartment of Molecular Medicine, The Scripps Research Institute, La Jolla, CA, 92073, USA.
Roman VlkolinskyDepartment of Molecular Medicine, The Scripps Research Institute, La Jolla, CA, 92073, USA.
Robert O MessingWaggoner Center for Alcohol and Addiction Research, Department of Neuroscience, The University of Texas at Austin, Austin, TX, 78712, USA.ORCID 0000-0002-5345-4431
Eric P ZorrillaDepartment of Molecular Medicine, The Scripps Research Institute, La Jolla, CA, 92073, USA.
Marisa RobertoDepartment of Molecular Medicine, The Scripps Research Institute, La Jolla, CA, 92073, USA. mroberto@scripps.edu.ORCID 0000-0003-0729-3961

Funding

Viral Vector CoreP60AA006420 · NIAAA · SCRIPPS RESEARCH INSTITUTE, THE · PI AMANDA J ROBERTS · 2003 to 2026
$46.3M
Neurpsychopharmacology-Multidisciplinary TrainingT32AA007456 · NIAAA · SCRIPPS RESEARCH INSTITUTE, THE · PI MARISA ROBERTO · 1985 to 2026
$13.4M
Electrophysiology of alcohol in extended amygdelaU01AA013498 · NIAAA · SCRIPPS RESEARCH INSTITUTE, THE · PI MARISA ROBERTO · 2001 to 2026
$12.6M
INIA: ANIMAL COREU01AA013520 · NIAAA · UNIVERSITY OF TEXAS AUSTIN · PI YURI A BLEDNOV, ROBERT O. MESSING · 2001 to 2026
$9.5M
Neuroplasticity of the Extended Amygdala CRF circuitry in alcohol dependenceR01AA021491 · NIAAA · SCRIPPS RESEARCH INSTITUTE, THE · PI ROBERTO, MARISA · 2013 to 2024
$3.9M
Gene-environment interaction: the brain CRF system in alcohol preferring msP ratsR37AA017447 · NIAAA · SCRIPPS RESEARCH INSTITUTE, THE · PI ROBERTO, MARISA · 2016 to 2025
$3.7M
Neuroimmune mechanisms in stress and alcohol comorbidityR01AA027700 · NIAAA · SCRIPPS RESEARCH INSTITUTE, THE · PI ROBERTO, MARISA · 2019 to 2023
$2.4M
Dorsal striatal phosphodiesterase 10A and compulsive ethanol useR01AA028879 · NIAAA · SCRIPPS RESEARCH INSTITUTE, THE · PI ZORRILLA, ERIC P · 2021 to 2025
$2.1M
Synaptic Mechanisms underlying sex-differences in alcohol use disorderR01AA029841 · NIAAA · SCRIPPS RESEARCH INSTITUTE, THE · PI MARISA ROBERTO · 2022 to 2026
$2.0M
Gene-environment interaction: the brain CRF system in alcohol preferring msP ratsR01AA017447 · NIAAA · SCRIPPS RESEARCH INSTITUTE, THE · PI ROBERTO, MARISA · 2009 to 2013
$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
Functional Studies of Subtypes of Parkinson's DiseaseeK23AG021491 · NIA · UNIV OF NORTH CAROLINA CHAPEL HILL · PI HUANG, XUEMEI · 2003 to 2007
$752k
NIAAA NIH HHS K99 AA026638NIAAA NIH HHS K99 AA030609NIAAA NIH HHS P60 AA006420NIAAA NIH HHS R01 AA017447NIAAA NIH HHS R01 AA021491NIAAA NIH HHS R01 AA026075NIAAA NIH HHS R01 AA027700NIAAA NIH HHS R01 AA028879NIAAA NIH HHS R01 AA029841NIAAA NIH HHS R21 AA029498NIAAA NIH HHS R37 AA017447NIAAA NIH HHS T32 AA007456NIAAA NIH HHS U01 AA013498NIAAA NIH HHS U01 AA013520U.S. Department of Health & Human Services | NIH | National Institute on Alcohol Abuse and Alcoholism (NIAAA) AA013498U.S. Department of Health & Human Services | NIH | National Institute on Alcohol Abuse and Alcoholism (NIAAA) AA017447U.S. Department of Health & Human Services | NIH | National Institute on Alcohol Abuse and Alcoholism (NIAAA) AA021491U.S. Department of Health & Human Services | NIH | National Institute on Alcohol Abuse and Alcoholism (NIAAA) AA02675U.S. Department of Health & Human Services | NIH | National Institute on Alcohol Abuse and Alcoholism (NIAAA) AA027700U.S. Department of Health & Human Services | NIH | National Institute on Alcohol Abuse and Alcoholism (NIAAA) AA028879U.S. Department of Health & Human Services | NIH | National Institute on Alcohol Abuse and Alcoholism (NIAAA) AA029498U.S. Department of Health & Human Services | NIH | National Institute on Alcohol Abuse and Alcoholism (NIAAA) AA029841
6 · The paper itself

Abstract

Post-traumatic stress disorder (PTSD) and alcohol use disorder (AUD) are often comorbid. Few treatments exist to reduce comorbid PTSD/AUD. Elucidating the mechanisms underlying their comorbidity could reveal new avenues for therapy. Here, we employed a model of comorbid PTSD/AUD, in which rats were subjected to a stressful shock in a familiar context followed by alcohol drinking. We then examined fear overgeneralization and irritability in these rats. Familiar context stress elevated drinking, increased fear overgeneralization, increased alcohol-related aggressive signs, and elevated peripheral stress hormones. We then examined transcripts of stress- and fear-relevant genes in the central amygdala (CeA), a locus that regulates stress-mediated alcohol drinking. Compared with unstressed rats, stressed rats exhibited increases in CeA transcripts for Crh and Fkbp5 and decreases in transcripts for Bdnf and Il18. Levels of Nr3c1 mRNA, which encodes the glucocorticoid receptor, increased in stressed males but decreased in stressed females. Transcripts of Il18 binding protein (Il18bp), Glp-1r, and genes associated with calcitonin gene-related peptide signaling (Calca, Ramp1, Crlr-1, and Iapp) were unaltered. Crh, but not Crhr1, mRNA was increased by stress; thus, we tested whether inhibiting CeA neurons that express corticotropin-releasing factor (CRF) suppress PTSD/AUD-like behaviors. We used Crh-Cre rats that had received a Cre-dependent vector encoding hM4D(Gi), an inhibitory Designer Receptors Exclusively Activated by Designer Drugs. Chemogenetic inhibition of CeA CRF neurons reduced alcohol intake but not fear overgeneralization or irritability-like behaviors. Our findings suggest that CeA CRF modulates PTSD/AUD comorbidity, and inhibiting CRF neural activity is primarily associated with reducing alcohol drinking but not trauma-related behaviors that are associated with PTSD/AUD.

Indexed as

Alcohol DrinkingAlcoholismCentral Amygdaloid NucleusCorticotropin-Releasing HormoneDisease Models, AnimalNeuronsStress Disorders, Post-TraumaticAmygdalaAnimalsEthanolFearFemaleMaleRatsRats, Sprague-DawleyStress, PsychologicalCorticotropin-Releasing HormoneEthanol

Identifiers

PMID38509197
PMCPMC11415545

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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.