Evidence map›Paper›PMID 34863917›Full record

ArticleAlcohol (Fayetteville, N.Y.)2022

Orbitofrontal cortex subregion inhibition during binge-like and aversion-resistant alcohol drinking.

Kristen M Schuh, Elizabeth A Sneddon, Austin M Nader, Marissa A Muench, Anna K Radke

Open access · greenAbstract read
In one paragraph

Article in Alcohol (Fayetteville, N.Y.), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.0field-weighted citation impact, top 27% 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

13 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. BDNF in ventrolateral orbitofrontal cortex to dorsolateral striatum circuit moderates alcohol consumption, seeking and relapse.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2026
    Article
  3. Article
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  7. Animal Models of Excessive Alcohol Consumption in Rodents.Current topics in behavioral neurosciences · 2025
    Review
  8. Punishment-resistant alcohol intake is mediated by the nucleus accumbens shell in female rats.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2024
    Article
  9. Article
  10. Article
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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

5 authors at 1 institution in 1 country.

Kristen M SchuhDepartment of Psychology and Center for Neuroscience and Behavior, Miami University, Oxford, OH, United States.
Elizabeth A SneddonDepartment of Psychology and Center for Neuroscience and Behavior, Miami University, Oxford, OH, United States.
Austin M NaderDepartment of Psychology and Center for Neuroscience and Behavior, Miami University, Oxford, OH, United States.
Marissa A MuenchDepartment of Psychology and Center for Neuroscience and Behavior, Miami University, Oxford, OH, United States.
Anna K RadkeDepartment of Psychology and Center for Neuroscience and Behavior, Miami University, Oxford, OH, United States. Electronic address: aradke@miamioh.edu.
Miami University · US

Funding

Analysis of subcortical networks that promote aversion-resistant alcohol drinkingR15AA027915 · NIAAA · MIAMI UNIVERSITY OXFORD · PI RADKE, ANNA KAY · 2020 to 2020
$378k
Mechanisms Underlying Female Vulnerability to Compulsive Alcohol DrinkingF99NS118727 · NINDS · MIAMI UNIVERSITY OXFORD · PI SNEDDON, ELIZABETH · 2021 to 2022
$84k
NIAAA NIH HHS R15 AA027915NINDS NIH HHS F99 NS118727
6 · The paper itself

Abstract

Two important contributors to alcohol-related problems and alcohol use disorder (AUD) are binge- and compulsive-like drinking. The orbitofrontal cortex (OFC), a brain region implicated in outcome valuation and behavioral flexibility, is functionally altered by alcohol exposure. Data from animal models also suggest that both the medial (mOFC) and lateral (lOFC) subregions of the OFC regulate alcohol-related behaviors. The current study was designed to examine the contributions of mOFC and lOFC using a model of binge-like and aversion-resistant ethanol drinking in C57BL/6J male and female mice. The inhibitory Designer Receptor Exclusively Activated by Designer Drugs (DREADD) hM4Di were used to inhibit neurons in either the mOFC or the lOFC in mice drinking 15% ethanol in a two-bottle, limited-access, modified drinking in the dark paradigm. The effects of chemogenetic inhibition on consumption of quinine-adulterated ethanol, water, and water + quinine were also assessed. Inhibiting the mOFC did not alter consumption of ethanol or aversion-resistant drinking of ethanol + quinine. In contrast, inhibition of neurons in the lOFC increased consumption, but not preference, of ethanol alone. mOFC and lOFC inhibition did not alter water or quinine-adulterated water intake, indicating the effects shown here are specific to ethanol drinking. These data support the role of the lOFC in regulating alcohol consumption but fail to find a similar role for mOFC.

Indexed as

AlcoholismBinge DrinkingAlcohol DrinkingAnimalsEthanolFemaleMaleMiceMice, Inbred C57BLPrefrontal CortexEthanolalcoholaversion-resistantbinge drinkingcompulsivedrinking in the darkorbitofrontal cortex

Identifiers

PMID34863917
PMCPMC8844094
OpenAlexW3217389595

What OpenQuestion holds

Textmetadata
LicenceTDM
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.