Evidence map›Paper›PMID 27185739›Full record

ArticleBehavioural brain research2016

Acute alcohol exposure during neurulation: Behavioral and brain structural consequences in adolescent C57BL/6J mice.

E W Fish, H T Holloway, A Rumple, L K Baker, L A Wieczorek, S S Moy, B Paniagua, S E Parnell

Open access · greenAbstract read
In one paragraph

Article in Behavioural brain research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed, 1 pooled it
11.1field-weighted citation impact, top 2% 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

26 citing papers in PubMed, 1 synthesis or guideline pooled it, 45 citations in OpenAlex.

  1. Pooled it
  2. Impact of Prenatal Alcohol Exposure on Cerebral Cortex Development.Advances in experimental medicine and biology · 2026
    Review
  3. Article
  4. Article
  5. Impact of Developmental Alcohol Exposure on the Thalamus.Advances in experimental medicine and biology · 2025
    Review
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  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
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  16. Article
  17. Review
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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

8 authors at 1 institution in 1 country.

E W FishBowles Center for Alcohol Studies (EWF, HTH, LKB, LAW, SEP), Department of Cell Biology and Physiology (SEP), Department of Psychiatry (AMR, SSM, BP), and Carolina Institute for Developmental Disabilities (SSM, BP, SEP), University of North Carolina, Chapel Hill, NC 27599, United States.
H T HollowayBowles Center for Alcohol Studies (EWF, HTH, LKB, LAW, SEP), Department of Cell Biology and Physiology (SEP), Department of Psychiatry (AMR, SSM, BP), and Carolina Institute for Developmental Disabilities (SSM, BP, SEP), University of North Carolina, Chapel Hill, NC 27599, United States.
A RumpleBowles Center for Alcohol Studies (EWF, HTH, LKB, LAW, SEP), Department of Cell Biology and Physiology (SEP), Department of Psychiatry (AMR, SSM, BP), and Carolina Institute for Developmental Disabilities (SSM, BP, SEP), University of North Carolina, Chapel Hill, NC 27599, United States.
L K BakerBowles Center for Alcohol Studies (EWF, HTH, LKB, LAW, SEP), Department of Cell Biology and Physiology (SEP), Department of Psychiatry (AMR, SSM, BP), and Carolina Institute for Developmental Disabilities (SSM, BP, SEP), University of North Carolina, Chapel Hill, NC 27599, United States.
L A WieczorekBowles Center for Alcohol Studies (EWF, HTH, LKB, LAW, SEP), Department of Cell Biology and Physiology (SEP), Department of Psychiatry (AMR, SSM, BP), and Carolina Institute for Developmental Disabilities (SSM, BP, SEP), University of North Carolina, Chapel Hill, NC 27599, United States.
S S MoyBowles Center for Alcohol Studies (EWF, HTH, LKB, LAW, SEP), Department of Cell Biology and Physiology (SEP), Department of Psychiatry (AMR, SSM, BP), and Carolina Institute for Developmental Disabilities (SSM, BP, SEP), University of North Carolina, Chapel Hill, NC 27599, United States.
B PaniaguaBowles Center for Alcohol Studies (EWF, HTH, LKB, LAW, SEP), Department of Cell Biology and Physiology (SEP), Department of Psychiatry (AMR, SSM, BP), and Carolina Institute for Developmental Disabilities (SSM, BP, SEP), University of North Carolina, Chapel Hill, NC 27599, United States.
S E ParnellBowles Center for Alcohol Studies (EWF, HTH, LKB, LAW, SEP), Department of Cell Biology and Physiology (SEP), Department of Psychiatry (AMR, SSM, BP), and Carolina Institute for Developmental Disabilities (SSM, BP, SEP), University of North Carolina, Chapel Hill, NC 27599, United States. Electronic address: sparnell@med.unc.edu.
North Carolina School of Science and Mathematics · US

Funding

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
NIAAA NIH HHS R00 AA018697NIAAA NIH HHS U01 AA017124NIAAA NIH HHS U01 AA021651NIBIB NIH HHS P41 EB015897
6 · The paper itself

Abstract

Prenatal alcohol exposure (PAE) can induce physical malformations and behavioral abnormalities that depend in part on thedevelopmental timing of alcohol exposure. The current studies employed a mouse FASD model to characterize the long-term behavioral and brain structural consequences of a binge-like alcohol exposure during neurulation; a first-trimester stage when women are typically unaware that they are pregnant. Time-mated C57BL/6J female mice were administered two alcohol doses (2.8g/kg, four hours apart) or vehicle starting at gestational day 8.0. Male and female adolescent offspring (postnatal day 28-45) were then examined for motor activity (open field and elevated plus maze), coordination (rotarod), spatial learning and memory (Morris water maze), sensory motor gating (acoustic startle and prepulse inhibition), sociability (three-chambered social test), and nociceptive responses (hot plate). Regional brain volumes and shapes were determined using magnetic resonance imaging. In males, PAE increased activity on the elevated plus maze and reduced social novelty preference, while in females PAE increased exploratory behavior in the open field and transiently impaired rotarod performance. In both males and females, PAE modestly impaired Morris water maze performance and decreased the latency to respond on the hot plate. There were no brain volume differences; however, significant shape differences were found in the cerebellum, hypothalamus, striatum, and corpus callosum. These results demonstrate that alcohol exposure during neurulation can have functional consequences into adolescence, even in the absence of significant brain regional volumetric changes. However, PAE-induced regional shape changes provide evidence for persistent brain alterations and suggest alternative clinical diagnostic markers.

Indexed as

AnimalsBrainCentral Nervous System DepressantsDisease Models, AnimalEthanolFemaleFetal Alcohol Spectrum DisordersMaleMaze LearningMice, Inbred C57BLNeurulationOrgan SizePain ThresholdPrepulse InhibitionSex FactorsSocial BehaviorCentral Nervous System DepressantsEthanolBehaviorBrainEthanolFetal alcohol spectrum disorderMouse

Identifiers

PMID27185739
PMCPMC4931949
OpenAlexW2356640336

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.