Evidence map›Paper›PMID 23675442›Full record

ArticlePloS one2013

Long-term effects of chronic intermittent ethanol exposure in adolescent and adult rats: radial-arm maze performance and operant food reinforced responding.

Mary-Louise Risher, Rebekah L Fleming, Nathalie Boutros, Svetlana Semenova, Wilkie A Wilson, Edward D Levin, Athina Markou, H Scott Swartzwelder, Shawn K Acheson

Abstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed, 1 pooled it
–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

49 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  12. Adolescent alcohol exposure alters threat avoidance in adulthood.Frontiers in behavioral neuroscience · 2022
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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

9 authors.

Mary-Louise RisherDepartment of Psychiatry and Behavioral Sciences, Duke University Medical Center, Durham, North Carolina, United States of America.
Rebekah L Fleming
Nathalie Boutros
Svetlana Semenova
Wilkie A Wilson
Edward D Levin
Athina Markou
H Scott Swartzwelder
Shawn K Acheson

Funding

Supp: Effects of Adolescent Alcohol Exposure on Hippocampal Function in AdulthoodU01AA019925 · NIAAA · DUKE UNIVERSITY · PI SWARTZWELDER, H SCOTT · 2010 to 2024
$5.0M
Impulsivity and reward in adult rats exposed to alcohol during adolescenceU01AA019970 · NIAAA · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI MARKOU, ATHINA · 2010 to 2014
$1.7M
Novel Prophylactic Pharmacotherapy in an Animal Model of Closed Head InjuryIK2BX001267 · VA · DURHAM VA MEDICAL CENTER · PI ACHESON, SHAWN · 2012 to 2016
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BLRD VA IK2 BX001267NIAAA NIH HHS U01 AA019925NIAAA NIH HHS U01-AA019925-01-NADIANIAAA NIH HHS U01 AA019970NIAAA NIH HHS U01-AA019970-NADIA
6 · The paper itself

Abstract

backgroundAdolescence is not only a critical period of late-stage neurological development in humans, but is also a period in which ethanol consumption is often at its highest. Given the prevalence of ethanol use during this vulnerable developmental period we assessed the long-term effects of chronic intermittent ethanol (CIE) exposure during adolescence, compared to adulthood, on performance in the radial-arm maze (RAM) and operant food-reinforced responding in male rats. METHODOLOGY/PRINCIPAL

findingsMale Sprague Dawley rats were exposed to CIE (or saline) and then allowed to recover. Animals were then trained in either the RAM task or an operant task using fixed- and progressive- ratio schedules. After baseline testing was completed all animals received an acute ethanol challenge while blood ethanol levels (BECs) were monitored in a subset of animals. CIE exposure during adolescence, but not adulthood decreased the amount of time that animals spent in the open portions of the RAM arms (reminiscent of deficits in risk-reward integration) and rendered animals more susceptible to the acute effects of an ethanol challenge on working memory tasks. The operant food reinforced task showed that these effects were not due to altered food motivation or to differential sensitivity to the nonspecific performance-disrupting effects of ethanol. However, CIE pre-treated animals had lower BEC levels than controls during the acute ethanol challenges indicating persistent pharmacokinetic tolerance to ethanol after the CIE treatment. There was little evidence of enduring effects of CIE alone on traditional measures of spatial and working memory. CONCLUSIONS/SIGNIFICANCE: These effects indicate that adolescence is a time of selective vulnerability to the long-term effects of repeated ethanol exposure on neurobehavioral function and acute ethanol sensitivity. The positive and negative findings reported here help to further define the nature and extent of the impairments observed after adolescent CIE and provide direction for future research.

Indexed as

AdolescentAdultAge FactorsAlcohol DrinkingAnimalsConditioning, OperantEthanolFoodHumansMaleMaze LearningMemoryRatsRats, Sprague-DawleyReinforcement, PsychologyRewardEthanol

Identifiers

PMID23675442
PMCPMC3652810

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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.