Evidence map›Paper›PMID 37433012›Full record

ArticleDevelopmental neurobiology

Exploring behavioral phenotypes in a mouse model of fetal alcohol spectrum disorders.

Tammy R Chaudoin, Stephen J Bonasera, Anna Dunaevsky, Ragunathan Padmashri

Open access · hybridAbstract read
In one paragraph

Article in Developmental neurobiology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.7field-weighted citation impact, top 14% 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

4 citing papers in PubMed, 3 citations in OpenAlex.

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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

4 authors at 2 institutions in 1 country.

Tammy R ChaudoinDepartment of Internal Medicine, Division of Geriatrics, University of Nebraska Medical Center, Omaha, Nebraska, USA.
Stephen J BonaseraDepartment of Internal Medicine, Division of Geriatrics, University of Nebraska Medical Center, Omaha, Nebraska, USA.
Anna DunaevskyDepartment of Neurological Sciences, University of Nebraska Medical Center, Omaha, Nebraska, USA.
Ragunathan PadmashriDepartment of Neurological Sciences, University of Nebraska Medical Center, Omaha, Nebraska, USA.ORCID 0000-0001-9497-3193
Nebraska Medical Center · USUniversity of Nebraska Medical Center · US

Funding

Translational Imaging and Behavioral Assessment (TIBA) CoreP20GM130447 · NIGMS · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI Anna Dunaevsky · 2020 to 2026
$20.7M
Effects of Developmental Alcohol Exposure on Astrocyte Ca2+ Signaling and Structural Synaptic PlasticityR21AA025751 · NIAAA · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI RAGUNATHAN, PADMASHRI · 2018 to 2019
$398k
NIAAA NIH HHS AA025751NIAAA NIH HHS R21 AA025751NIGMS NIH HHS P20 GM130447
6 · The paper itself

Abstract

Fetal alcohol spectrum disorders are one of the leading causes of developmental abnormalities worldwide. Maternal consumption of alcohol during pregnancy leads to a diverse range of cognitive and neurobehavioral deficits. Although moderate-to-heavy levels of prenatal alcohol exposure (PAE) have been associated with adverse offspring outcomes, there is limited data on the consequences of chronic low-level PAE. Here, we use a model of maternal voluntary alcohol consumption throughout gestation in a mouse model to investigate the effects of PAE on behavioral phenotypes during late adolescence and early adulthood in male and female offspring. Body composition was measured by dual-energy X-ray absorptiometry. Baseline behaviors, including feeding, drinking, and movement, were examined by performing home cage monitoring studies. The impact of PAE on motor function, motor skill learning, hyperactivity, acoustic reactivity, and sensorimotor gating was investigated by performing a battery of behavioral tests. PAE was found to be associated with altered body composition. No differences in overall movement, food, or water consumption were observed between control and PAE mice. Although PAE offspring of both sexes exhibited deficits in motor skill learning, no differences were observed in basic motor skills such as grip strength and motor coordination. PAE females exhibited a hyperactive phenotype in a novel environment. PAE mice exhibited increased reactivity to acoustic stimuli, and PAE females showed disrupted short-term habituation. Sensorimotor gating was not altered in PAE mice. Collectively, our data show that chronic low-level exposure to alcohol in utero results in behavioral impairments.

Indexed as

Fetal Alcohol Spectrum DisordersPrenatal Exposure Delayed EffectsAnimalsEthanolFemaleHumansLearningMaleMicePhenotypePregnancyEthanolbehaviorbody compositionfetal alcohol spectrum disordersneurodevelopmentprenatal alcohol exposure

Identifiers

PMID37433012
PMCPMC10546278
OpenAlexW4383875252

What OpenQuestion holds

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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.