Evidence map›Paper›PMID 20842647›Full record

ArticleBirth defects research. Part A, Clinical and molecular teratology2010

Magnetic resonance microscopy-based analyses of the brains of normal and ethanol-exposed fetal mice.

Shonagh K O'Leary-Moore, Scott E Parnell, Elizabeth A Godin, Deborah B Dehart, Jacob J Ament, Amber A Khan, G Allan Johnson, Martin A Styner, Kathleen K Sulik

Open access · greenAbstract read
In one paragraph

Article in Birth defects research. Part A, Clinical and molecular teratology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
7.6field-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

44 citing papers in PubMed, 64 citations in OpenAlex.

  1. Animal Models of Prenatal Alcohol Exposure.Advances in experimental medicine and biology · 2026
    Review
  2. Impact of Prenatal Alcohol Exposure on Cerebral Cortex Development.Advances in experimental medicine and biology · 2026
    Review
  3. Article
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  10. Patterns of Prenatal Alcohol Exposure and Alcohol-Related Dysmorphic Features.Alcoholism, clinical and experimental research · 2020
    Article
  11. Article
  12. In utero MRI identifies consequences of early-gestation alcohol drinking on fetal brain development in rhesus macaques.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  13. Article
  14. Article
  15. Article
  16. Effects of prenatal alcohol exposure (PAE): insights into FASD using mouse models of PAE.Biochemistry and cell biology = Biochimie et biologie cellulaire · 2018
    Review
  17. Article
  18. Article
  19. Article
  20. Review
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 at 2 institutions in 1 country.

Shonagh K O'Leary-MooreFetal Toxicology Division,Bowles Center for Alcohol Studies, University of North Carolina at Chapel Hill,Chapel Hill, NC 27599-7178E, USA. somoore@med.unc.edu
Scott E Parnell
Elizabeth A Godin
Deborah B Dehart
Jacob J Ament
Amber A Khan
G Allan Johnson
Martin A Styner
Kathleen K Sulik
University of North Carolina at Chapel Hill · USDuke University · US

Funding

UNC ARC Information/Dissemination CoreP60AA011605 · NIAAA · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Melissa A Herman · 2003 to 2026
$46.3M
UNC MRDD Research CenterP30HD003110 · NICHD · UNIV OF NORTH CAROLINA CHAPEL HILL · PI BELGER, AYSENIL · 1985 to 2012
$28.7M
X-RAY RESEARCH AND DEVELOPMENT WITH/WITHOUT LIVE ANIMALSP41RR005959 · NCRR · DUKE UNIVERSITY · PI DZAU, VICTOR J · 1990 to 2011
$16.0M
Supplement to Molecular and Cellular Studies on Alcohol's ActionsT32AA007573 · NIAAA · UNIV OF NORTH CAROLINA CHAPEL HILL · PI FULTON T CREWS, Thomas L. Kash · 1997 to 2026
$9.3M
MOLECULAR AND CELLULAR PATHOGENESIS IN ALCOHOLISMP50AA011605 · NIAAA · UNIVERSITY OF NORTH CAROLINA CHAPEL HILL · PI CREWS, FULTON T · 1998 to 2002
$4.9M
Small Animal Imaging Resource ProgramU24CA092656 · NCI · DUKE UNIVERSITY · PI JOHNSON, GEORGE ALLAN · 2007 to 2011
$2.2M
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
NCI NIH HHS U24 CA092656NCRR NIH HHS P41 RR005959NIAAA NIH HHS AA007573NIAAA NIH HHS P50 AA011605NIAAA NIH HHS P60 AA011605NIAAA NIH HHS R00 AA018697NIAAA NIH HHS T32 AA007573NIAAA NIH HHS U01 AA017124NICHD NIH HHS HD 03110NICHD NIH HHS P30 HD003110PHS HHS P41 05959
6 · The paper itself

Abstract

backgroundThe application of magnetic resonance microscopy (MRM) to the study of normal and abnormal prenatal mouse development has facilitated discovery of dysmorphology following prenatal ethanol insult. The current analyses extend this work, providing a regional brain volume-based description of normal brain growth and illustrating the consequences of gestational day (GD) 10 ethanol exposure in the fetal mouse.

methodsTo assess normal growth, control C57Bl/6J fetuses collected on GD 16, GD 16.5, and GD 17 were scanned using a 9.4-T magnet, resulting in 29-μm isotropic resolution images. For the ethanol teratogenicity studies, C57Bl/6J dams were administered intraperitoneal ethanol (2.9 g/kg) at 10 days, 0 hr, and 10 days, 4 hr, after fertilization, and fetuses were collected for analyses on GD 17. From individual MRM scans, linear measurements and regional brain volumes were determined and compared.

resultsIn control fetuses, each of the assessed brain regions increased in volume, whereas ventricular volumes decreased between GD 16 and GD 17. Illustrating a global developmental delay, prenatal ethanol exposure resulted in reduced body volumes, crown-rump lengths, and a generalized decrease in regional brain volumes compared with GD 17 controls. However, compared with GD 16.5, morphologically matched controls, ethanol exposure resulted in volume increases in the lateral and third ventricles as well as a disproportionate reduction in cortical volume.

conclusionsThe normative data collected in this study facilitate the distinction between GD 10 ethanol-induced developmental delay and frank dysmorphology. This work illustrates the utility of MRM-based analyses for developmental toxicology studies and extends our knowledge of the stage-dependency of ethanol teratogenesis.

Indexed as

Abnormalities, Drug-InducedAnimalsBrainDisease Models, AnimalEthanolFemaleFetal Alcohol Spectrum DisordersFetusGestational AgeHumansMagnetic Resonance ImagingMaleMiceMice, Inbred C57BLMicroscopyPregnancyEthanol

Identifiers

PMID20842647
PMCPMC3445267
OpenAlexW1999513172

What OpenQuestion holds

Textmetadata
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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.