Evidence map›Paper›PMID 25746516›Full record

ArticleBehavioural brain research2015

Docosahexaenoic acid partially ameliorates deficits in social behavior and ultrasonic vocalizations caused by prenatal ethanol exposure.

Kristen A Wellmann, Finney George, Fares Brnouti, Sandra M Mooney

Erratum issuedAbstract read
In one paragraph

Article in Behavioural brain research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
9.2field-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

28 citing papers in PubMed, 50 citations in OpenAlex.

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  9. Behavioral changes inFrontiers in neuroscience · 2023
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors at 1 institution in 1 country.

Kristen A WellmannDepartment of Pediatrics, University of Maryland, Baltimore, MD 21201, United States. Electronic address: kwellmann@peds.umaryland.edu.
Finney GeorgeDepartment of Pediatrics, University of Maryland, Baltimore, MD 21201, United States.
Fares BrnoutiDepartment of Pediatrics, University of Maryland, Baltimore, MD 21201, United States.
Sandra M MooneyDepartment of Pediatrics, University of Maryland, Baltimore, MD 21201, United States. Electronic address: smooney@peds.umaryland.edu.
University of Maryland, Baltimore · US

Funding

EXPERIMENTAL FETAL ALCOHOL SYNDROME: CEREBRAL CORTEXR01AA006916 · NIAAA · UPSTATE MEDICAL UNIVERSITY · PI MIDDLETON, FRANK A., MOONEY, SANDRA M · 1985 to 2014
$4.5M
Experimental Factors in Fetal Alcohol Spectrum DisorderR01AA022413 · NIAAA · UNIV OF NORTH CAROLINA CHAPEL HILL · PI MOONEY, SANDRA M · 2014 to 2018
$1.7M
Effects of developmental ethanol exposure on brain developmentR01AA018693 · NIAAA · UPSTATE MEDICAL UNIVERSITY · PI MOONEY, SANDRA M · 2010 to 2014
$1.2M
NIAAA NIH HHS AA018693NIAAA NIH HHS AA022413NIAAA NIH HHS R01 AA006916NIAAA NIH HHS R01 AA018693NIAAA NIH HHS R01 AA022413
6 · The paper itself

Abstract

Prenatal ethanol exposure disrupts social behavior in humans and rodents. One system particularly important for social behavior is the somatosensory system. Prenatal ethanol exposure alters the structure and function of this area. Docosahexaenoic acid (DHA), an omega 3 polyunsaturated fatty acid, is necessary for normal brain development and brains from ethanol-exposed animals are DHA deficient. Thus, we determined whether postnatal DHA supplementation ameliorated behavioral deficits induced by prenatal ethanol exposure. Timed pregnant Long-Evans rats were assigned to one of three groups: ad libitum access to an ethanol-containing liquid diet, pair fed an isocaloric isonutritive non-alcohol liquid diet, or ad libitum access to chow and water. Pups were assigned to one of two postnatal treatment groups; gavaged intragastrically once per day between postnatal day (P)11 and P20 with DHA (10 mg/kg in artificial rat milk) or artificial rat milk. A third group was left untreated. Isolation-induced ultrasonic vocalizations (iUSVs) were recorded on P14. Social behavior and play-induced USVs were tested on P28 or P42. Somatosensory performance was tested with a gap crossing test around P33 or on P42. Anxiety was tested on elevated plus maze around P35. Animals exposed to ethanol prenatally vocalized less, play fought less, and crossed a significantly shorter gap than control-treated animals. Administration of DHA ameliorated these ethanol-induced deficits such that the ethanol-exposed animals given DHA were no longer significantly different to control-treated animals. Thus, DHA administration may have therapeutic value to reverse some of ethanol's damaging effects.

Indexed as

AnimalsAnxietyCentral Nervous System DepressantsDocosahexaenoic AcidsEthanolFemaleFetal Alcohol Spectrum DisordersPregnancyPrenatal Exposure Delayed EffectsPsychotropic DrugsRandom AllocationRats, Long-EvansSocial BehaviorSocial IsolationUltrasonicsVocalization, AnimalCentral Nervous System DepressantsDocosahexaenoic AcidsEthanolPsychotropic DrugsDHAFetal alcohol syndromeOmega 3 polyunsaturated fatty acidSocial interaction

Identifiers

PMID25746516
PMCPMC4392387
OpenAlexW2002093099

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.