Evidence map›Paper›PMID 27695144›Full record

ArticleAlcoholism, clinical and experimental research2014

The Effect of mGluR5 Antagonism During Binge Drinkingon Subsequent Ethanol Intake in C57BL/6J Mice: Sex- and Age-Induced Differences.

Debra K Cozzoli, Moriah N Strong-Kaufman, Michelle A Tanchuck, Joel G Hashimoto, Kristine M Wiren, Deborah A Finn

Open access · greenAbstract read
In one paragraph

Article in Alcoholism, clinical and experimental research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
0.4field-weighted citation impact, top 41% 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

22 citing papers in PubMed, 26 citations in OpenAlex.

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  11. Adolescent alcohol exposure produces sex differences in negative affect-like behavior and group I mGluR BNST plasticity.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2020
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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

6 authors at 2 institutions in 1 country.

Debra K CozzoliDepartment of Behavioral Neuroscience (DKC, MNS-K, MAT, JGH, KMW, DAF), Oregon Health & Science University, Portland, Oregon; Department of Veterans Affairs Medical Research (JGH, KMW, DAF), Veterans Affairs Medical Center, Portland, Oregon; and Portland Alcohol Research Center (DAF), Portland, Oregon.
Moriah N Strong-KaufmanDepartment of Behavioral Neuroscience (DKC, MNS-K, MAT, JGH, KMW, DAF), Oregon Health & Science University, Portland, Oregon; Department of Veterans Affairs Medical Research (JGH, KMW, DAF), Veterans Affairs Medical Center, Portland, Oregon; and Portland Alcohol Research Center (DAF), Portland, Oregon.
Michelle A TanchuckDepartment of Behavioral Neuroscience (DKC, MNS-K, MAT, JGH, KMW, DAF), Oregon Health & Science University, Portland, Oregon; Department of Veterans Affairs Medical Research (JGH, KMW, DAF), Veterans Affairs Medical Center, Portland, Oregon; and Portland Alcohol Research Center (DAF), Portland, Oregon.
Joel G HashimotoDepartment of Behavioral Neuroscience (DKC, MNS-K, MAT, JGH, KMW, DAF), Oregon Health & Science University, Portland, Oregon; Department of Veterans Affairs Medical Research (JGH, KMW, DAF), Veterans Affairs Medical Center, Portland, Oregon; and Portland Alcohol Research Center (DAF), Portland, Oregon.
Kristine M WirenDepartment of Behavioral Neuroscience (DKC, MNS-K, MAT, JGH, KMW, DAF), Oregon Health & Science University, Portland, Oregon; Department of Veterans Affairs Medical Research (JGH, KMW, DAF), Veterans Affairs Medical Center, Portland, Oregon; and Portland Alcohol Research Center (DAF), Portland, Oregon.
Deborah A FinnDepartment of Behavioral Neuroscience (DKC, MNS-K, MAT, JGH, KMW, DAF), Oregon Health & Science University, Portland, Oregon; Department of Veterans Affairs Medical Research (JGH, KMW, DAF), Veterans Affairs Medical Center, Portland, Oregon; and Portland Alcohol Research Center (DAF), Portland, Oregon.
Oregon Health & Science University · USVeterans Health Administration · US

Funding

Translational measures of risk for excessive alcohol consumptionP60AA010760 · NIAAA · OREGON HEALTH & SCIENCE UNIVERSITY · PI Suzanne S. Fei · 2006 to 2026
$34.5M
BIOLOGICAL BASES OF ALCOHOLISMT32AA007468 · NIAAA · OREGON HEALTH & SCIENCE UNIVERSITY · PI Andrey E Ryabinin · 1987 to 2026
$11.3M
Adolescent Binge Drinking Increases Adult Alcohol Intake: Glutamate MechanismsI01BX001070 · VA · PORTLAND VA MEDICAL CENTER · PI FINN, DEBORAH A. · 2011 to 2014
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Expression Differences During Abstinence Predict Risk Of Alcohol RelapseI01BX001172 · VA · PORTLAND VA MEDICAL CENTER · PI WIREN, KRISTINE M. · 2012 to 2015
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BLRD VA I01 BX001070BLRD VA I01 BX001172Intramural VA VA999999NIAAA NIH HHS P60 AA010760NIAAA NIH HHS T32 AA007468United States BLRDUnited States Intramural VA
6 · The paper itself

Abstract

backgroundBinge ethanol (EtOH) intake during adolescence leads to an array of behavioral and cognitive consequences including elevated intake of EtOH during adulthood, with female mice showing greater susceptibility than males. Administration of the metabotropic glutamate receptor 5 (mGluR5) antagonist 3-((2-Methyl-1,3-thiazol-4-yl)ethynyl)pyridine (MTEP) has been shown to reduce EtOH self-administration in adult male mice, but little is known about its effect on female and adolescent mice.

methodsMTEP (0, 10, 20 mg/kg, i.p.) was repeatedly administered to female and male, adult and adolescent C57BL/6J mice during binge sessions using the scheduled high alcohol consumption paradigm. Next, we assessed whether MTEP administration during binge altered the subsequent 24-hour EtOH intake following a period of abstinence. Finally, we investigated whether MTEP administration during binge followed by an abstinence period altered mRNA of glutamatergic genes within the nucleus accumbens of female mice.

resultsMTEP significantly decreased binge EtOH intake in all mice, but only female mice exhibited altered subsequent 24-hour EtOH intake. Interestingly, the alteration in subsequent EtOH intake in female animals was age dependent, with adolescent exposure to MTEP during binge decreasing 24-hour intake and adult exposure to MTEP during binge increasing 24-hour intake. Finally, while there were no effects of MTEP pretreatment on the genes examined, there was a robust age effect found during analysis of mGluR1 (

conclusionsCollectively, the present findings add to existing evidence implicating the contribution of long-term effects of adolescent binge drinking to enhance alcohol abuse in adulthood, while suggesting that mGluR5 antagonism may not be the best pharmacotherapy to treat binge alcohol consumption in female and adolescent animals.

Indexed as

Age FactorsAnimalsBinge DrinkingEthanolFemaleGene ExpressionMaleMiceMice, Inbred C57BLModels, AnimalNucleus AccumbensPyridinesReceptor, Metabotropic Glutamate 5Receptors, N-Methyl-D-AspartateRNA, MessengerSex Factors3-((2-methyl-1,3-thiazol-4-yl)ethynyl)pyridineEthanolGrm5 protein, mousePyridinesReceptor, Metabotropic Glutamate 5Receptors, N-Methyl-D-AspartateRNA, MessengerThiazolesAdolescentAdultAlcoholGlutamateMTEP

Identifiers

PMID27695144
PMCPMC5041302
OpenAlexW2081280243

What OpenQuestion holds

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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.