Evidence map›Paper›PMID 29107713›Full record

ArticleBehavioural brain research2018

The enduring impact of neurulation stage alcohol exposure: A combined behavioral and structural neuroimaging study in adult male and female C57BL/6J mice.

E W Fish, L A Wieczorek, A Rumple, M Suttie, S S Moy, P Hammond, S E Parnell

Abstract read
In one paragraph

Article in Behavioural brain research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing 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

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

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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

7 authors.

E W FishThe Bowles Center for Alcohol Studies (EWF, LAW, SEP), Department of Cell Biology and Physiology (SEP), Department of Psychiatry (AR, SSM), and Carolina Institute for Developmental Disabilities (SSM, SEP), University of North Carolina, Chapel Hill, NC 27599, United States. Electronic address: efish@med.unc.edu.
L A WieczorekThe Bowles Center for Alcohol Studies (EWF, LAW, SEP), Department of Cell Biology and Physiology (SEP), Department of Psychiatry (AR, SSM), and Carolina Institute for Developmental Disabilities (SSM, SEP), University of North Carolina, Chapel Hill, NC 27599, United States.
A RumpleThe Bowles Center for Alcohol Studies (EWF, LAW, SEP), Department of Cell Biology and Physiology (SEP), Department of Psychiatry (AR, SSM), and Carolina Institute for Developmental Disabilities (SSM, SEP), University of North Carolina, Chapel Hill, NC 27599, United States.
M SuttieNuffield Department of Obstetrics and Gynaecology, University of Oxford, Oxford, UK.
S S MoyThe Bowles Center for Alcohol Studies (EWF, LAW, SEP), Department of Cell Biology and Physiology (SEP), Department of Psychiatry (AR, SSM), and Carolina Institute for Developmental Disabilities (SSM, SEP), University of North Carolina, Chapel Hill, NC 27599, United States.
P HammondNuffield Department of Obstetrics and Gynaecology, University of Oxford, Oxford, UK.
S E ParnellThe Bowles Center for Alcohol Studies (EWF, LAW, SEP), Department of Cell Biology and Physiology (SEP), Department of Psychiatry (AR, SSM), and Carolina Institute for Developmental Disabilities (SSM, SEP), University of North Carolina, Chapel Hill, NC 27599, United States.

Funding

UNC ARC Information/Dissemination CoreP60AA011605 · NIAAA · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Thomas L. Kash · 2003 to 2026
$46.3M
Preclinical CoreU54HD079124 · NICHD · UNIV OF NORTH CAROLINA CHAPEL HILL · PI LI, YUN · 2013 to 2019
$8.0M
INTEGRATED CENTER FOR IN VIVO MICROSCOPYP41EB015897 · NIBIB · DUKE UNIVERSITY · PI JOHNSON, GEORGE ALLAN · 2012 to 2017
$7.4M
Exploring the Genetics of FASD in Complementary Mouse and Fish ModelsU01AA021651 · NIAAA · UNIV OF NORTH CAROLINA CHAPEL HILL · PI EBERHART, JOHANN K, PARNELL, SCOTT · 2012 to 2021
$3.2M
MAGNETIC RESONANCE AND DIFFUSION TENSOR IMAGING OF A MOUSE FASD MODEL U01U01AA017124 · NIAAA · UNIV OF NORTH CAROLINA CHAPEL HILL · PI SULIK, KATHLEEN K · 2007 to 2011
$1.2M
Neuroanatomical/Functional Correlates in an FASD ModelR00AA018697 · NIAAA · UNIV OF NORTH CAROLINA CHAPEL HILL · PI PARNELL, SCOTT · 2012 to 2014
$710k
Neuroanatomical/Functional Correlates in an FASD ModelK99AA018697 · NIAAA · UNIV OF NORTH CAROLINA CHAPEL HILL · PI PARNELL, SCOTT · 2010 to 2011
$180k
NIAAA NIH HHS K99 AA018697NIAAA NIH HHS P60 AA011605NIAAA NIH HHS R00 AA018697NIAAA NIH HHS U01 AA017124NIAAA NIH HHS U01 AA021651NIBIB NIH HHS P41 EB015897NICHD NIH HHS U54 HD079124
6 · The paper itself

Abstract

Prenatal alcohol exposure (PAE) can cause behavioral and brain alterations over the lifespan. In animal models, these effects can occur following PAE confined to critical developmental periods, equivalent to the third and fourth weeks of human gestation, before pregnancy is usually recognized. The current study focuses on PAE during early neurulation and examines the behavioral and brain structural consequences that appear in adulthood. On gestational day 8 C57BL/6J dams received two alcohol (2.8g/kg, i.p), or vehicle, administrations, four hours apart. Male and female offspring were reared to adulthood and examined for performance on the elevated plus maze, rotarod, open field, Morris water maze, acoustic startle, social preference (i.e. three-chambered social approach test), and the hot plate. A subset of these mice was later evaluated using magnetic resonance imaging to detect changes in regional brain volumes and shapes. In males, PAE increased exploratory behaviors on the elevated plus maze and in the open field; these changes were associated with increased fractional anisotropy in the anterior commissure. In females, PAE reduced social preference and the startle response, and decreased cerebral cortex and brain stem volumes. Vehicle-treated females had larger pituitaries than did vehicle-treated males, but PAE attenuated this sex difference. In males, pituitary size correlated with open field activity, while in females, pituitary size correlated with social activity. These findings indicate that early neurulation PAE causes sex specific behavioral and brain changes in adulthood. Changes in the pituitary suggest that this structure is especially vulnerable to neurulation stage PAE.

Indexed as

Social BehaviorAnimalsBehavior, AnimalBrainEthanolExploratory BehaviorFemaleMagnetic Resonance ImagingMaleMiceNeurulationOrgan SizePregnancyPrenatal Exposure Delayed EffectsSex FactorsEthanolBehaviorBrainEthanolFetal alcohol spectrum disorderMouse

Identifiers

PMID29107713
PMCPMC5726510

What OpenQuestion holds

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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.