Evidence map›Paper›PMID 32482639›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2020

Estrogen Receptor α Regulates Ethanol Excitation of Ventral Tegmental Area Neurons and Binge Drinking in Female Mice.

Bertha J Vandegrift, Elisa R Hilderbrand, Rosalba Satta, Rex Tai, Donghong He, Chang You, Hu Chen, Pingwen Xu, Cassandre Coles, Mark S Brodie and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
6.1field-weighted citation impact, top 3% 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

48 citing papers in PubMed, 66 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. The role of ovarian hormones in risk aversion in female rats.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2026
    Article
  6. Article
  7. Review
  8. Article
  9. Stress and parental behaviors.Neuroscience research · 2025
    Review
  10. Review
  11. Reward Neurocircuitry Predicts Longitudinal Changes in Alcohol Use Following Trauma Exposure.Biological psychiatry. Cognitive neuroscience and neuroimaging · 2025
    Article
  12. Article
  13. Adolescent Alcohol Exposure Dysregulates Developing Cortical GABA Circuits.Advances in experimental medicine and biology · 2025
    Review
  14. Article
  15. Parvalbumin interneuron mGluNeuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2024
    Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

11 authors at 4 institutions in 4 countries.

Bertha J VandegriftCenter for Alcohol Research in Epigenetics and Department of Psychiatry.
Elisa R HilderbrandCenter for Alcohol Research in Epigenetics and Department of Psychiatry.
Rosalba SattaCenter for Alcohol Research in Epigenetics and Department of Psychiatry.
Rex TaiCenter for Alcohol Research in Epigenetics and Department of Psychiatry.
Donghong HeCenter for Alcohol Research in Epigenetics and Department of Psychiatry.
Chang YouDepartment of Physiology and Biophysics.
Hu ChenCenter for Alcohol Research in Epigenetics and Department of Psychiatry.
Pingwen XuDepartment of Medicine, Division of Endocrinology, Diabetes and Metabolism, University of Illinois at Chicago, Chicago, Illinois 60612.
Cassandre ColesCenter for Alcohol Research in Epigenetics and Department of Psychiatry.
Mark S BrodieCenter for Alcohol Research in Epigenetics and Department of Psychiatry.
Amy W LasekCenter for Alcohol Research in Epigenetics and Department of Psychiatry alasek@uic.edu.ORCID 0000-0002-7099-2442
Epigénétique et Destin Cellulaire · FREpigenomics (Germany) · DEInstitute of Molecular Biology and Biophysics · RUUniversity of Illinois Chicago · US

Funding

Strengthening Stakeholder Engagement in Human Research Protections.UL1TR002003 · NCATS · UNIVERSITY OF ILLINOIS AT CHICAGO · PI KARNIK, NIRANJAN SUBHASH, MERMELSTEIN, ROBIN J. · 2016 to 2024
$33.7M
Pilot Project Program P50AA022538 · NIAAA · UNIVERSITY OF ILLINOIS AT CHICAGO · PI DENNIS R GRAYSON · 2015 to 2026
$21.3M
Regulation of Excessive Alcohol Consumption by the Lmo-Alk AxisU01AA020912 · NIAAA · VIRGINIA COMMONWEALTH UNIVERSITY · PI Amy Wolven Lasek · 2011 to 2026
$5.4M
Mechanisms of Estrogen Action in Enhancing Behavioral Responses to CocaineR01DA033429 · NIDA · UNIVERSITY OF ILLINOIS AT CHICAGO · PI LASEK, AMY WOLVEN · 2012 to 2016
$1.7M
The role of amygdalar estrogen receptors in ethanol reward and binge drinkingF31AA024344 · NIAAA · UNIVERSITY OF ILLINOIS AT CHICAGO · PI HILDERBRAND, ELISA R. · 2016 to 2017
$80k
NCATS NIH HHS UL1 TR002003NIAAA NIH HHS F31 AA024344NIAAA NIH HHS P50 AA022538NIAAA NIH HHS U01 AA020912NIDA NIH HHS R01 DA033429
6 · The paper itself

Abstract

Elevations in estrogen (17β-estradiol, E2) are associated with increased alcohol drinking by women and experimentally in rodents. E2 alters the activity of the dopamine system, including the VTA and its projection targets, which plays an important role in binge drinking. A previous study demonstrated that, during high E2 states, VTA neurons in female mice are more sensitive to ethanol excitation. However, the mechanisms responsible for the ability of E2 to enhance ethanol sensitivity of VTA neurons have not been investigated. In this study, we used selective agonists and antagonists to examine the role of ER subtypes (ERα and ERβ) in regulating the ethanol sensitivity of VTA neurons in female mice and found that ERα promotes the enhanced ethanol response of VTA neurons. We also demonstrated that enhancement of ethanol excitation requires the activity of the metabotropic glutamate receptor, mGluR1, which is known to couple with ERα at the plasma membrane. To investigate the behavioral relevance of these findings, we administered lentivirus-expressing short hairpin RNAs targeting either ERα or ERβ into the VTA and found that knockdown of each receptor in the VTA reduced binge-like ethanol drinking in female, but not male, mice. Reducing ERα in the VTA had a more dramatic effect on binge-like drinking than reducing ERβ, consistent with the ability of ERα to alter ethanol sensitivity of VTA neurons. These results provide important insight into sex-specific mechanisms that drive excessive alcohol drinking.

Indexed as

AnimalsBinge DrinkingCell MembraneCentral Nervous System DepressantsEstrogen AntagonistsEstrogen Receptor alphaEstrogen Receptor betaEthanolFemaleGene Knockdown TechniquesHumansMaleMiceMice, Inbred C57BLNeuronsOvariectomyCentral Nervous System DepressantsEsr1 protein, mouseEstrogen AntagonistsEstrogen Receptor alphaEstrogen Receptor betaEthanolReceptors, AMPAalcoholdopamineestrogenestrogen receptorssex differences

Identifiers

PMID32482639
PMCPMC7329299
OpenAlexW3030925002

What OpenQuestion holds

Textmetadata
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.