Evidence map›Paper›PMID 41237071›Full record

ArticleDevelopmental neuroscience2025

Abnormal Magnetic Resonance Imaging in the Medial Prefrontal Cortex following Prenatal Alcohol Exposure and Placental Insufficiency in a Preclinical Model.

Zarena M Dominguez, Suzy Davies, Yousuf Amer, Riddhi Patel, Hawley Helmbrecht, Anyah E Rivera, Lauren L Jantzie, Daniel D Savage, Jessie R Maxwell

Abstract read
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Article in Developmental neuroscience, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Zarena M DominguezDivision of Neonatology, Department of Pediatrics, University of New Mexico, Albuquerque, New Mexico, USA.
Suzy DaviesDivision of Neonatology, Department of Pediatrics, University of New Mexico, Albuquerque, New Mexico, USA.
Yousuf AmerDivision of Neonatology, Department of Pediatrics, University of New Mexico, Albuquerque, New Mexico, USA.
Riddhi PatelNeonatal-Perinatal Medicine, Department of Pediatrics, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Hawley HelmbrechtNeonatal-Perinatal Medicine, Department of Pediatrics, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Anyah E RiveraNeonatal-Perinatal Medicine, Department of Pediatrics, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Lauren L JantzieNeonatal-Perinatal Medicine, Department of Pediatrics, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Daniel D SavageDivision of Neonatology, Department of Pediatrics, University of New Mexico, Albuquerque, New Mexico, USA.
Jessie R MaxwellDivision of Neonatology, Department of Pediatrics, University of New Mexico, Albuquerque, New Mexico, USA, jrmaxwell@salud.unm.edu.

Funding

UNM HSC Clinical and Translational Science CenterUL1TR001449 · NCATS · UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR · PI CAMPEN, MATTHEW J, PANDHI, NANCY · 2015 to 2024
$36.9M
Understanding neurophysiological deficits in response inhibition in children with FASDP50AA022534 · NIAAA · UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR · PI Carlos Fernando Valenzuela · 2014 to 2026
$21.5M
Consequences of combined prenatal alcohol exposure and acute placental ischemia on frontal cortical-sensitive behavior, structure, and physiology in juvenile offspringK08AA030080 · NIAAA · UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR · PI Jessie R. Maxwell · 2022 to 2026
$968k
NCATS NIH HHS UL1 TR001449NIAAA NIH HHS K08 AA030080NIAAA NIH HHS P50 AA022534
6 · The paper itself

Abstract

introductionThe combination of prenatal alcohol exposure (PAE) and placental insufficiency (PI) places infants at an increased risk for preterm birth and may worsen brain injury and neurobehavioral outcomes. In this preclinical study, the effect of PAE + PI on lateral, medial, and ventral prefrontal cortex (PFC), striatum and corpus callosum microstructure were investigated using diffusion tensor imaging (DTI). These brain regions are important for executive and higher cognitive functions, like cognitive flexibility.

methodsPregnant Long-Evans rat dams voluntarily drank 5% ethanol in saccharin water or plain saccharin water until embryonic day 18 (E18) to mimic moderate PAE. On E19, an open laparotomy was completed, and the uterine arteries were transiently occluded for 1 h. The dams in the sham group underwent the same procedure, but without uterine artery occlusion. Offspring are delivered normally on E22 and matured with their dams. On postnatal day 35 (P35), tissue was collected from male and female rat offspring from all four prenatal treatment groups (Sham, PAE, PI, and PAE+PI). Fixed brain tissue was then scanned ex vivo on a Bruker 11.7 T magnetic resonance imaging. Fractional anisotropy (FA) and directional diffusion were measured in regions of interest. Two-way analysis of variance with Tukey's correction was used, with p < 0.05 significant.

resultsDTI analyses of the medial PFC (n = 14-30/group) revealed a significant impact of the prenatal exposure/insult on the FA (p < 0.05), with sham having the lowest FA (0.24 ± 0.01) and PI having the highest FA (0.28 ± 0.02) as well as a lower mean diffusivity (MD; 3.32 × 10-4 ± 2.35 × 10-5 mm2/s; p < 0.01) compared to PAE (4.35 × 10-4 ± 1.47 × 10-5 mm2/s). The lateral PFC was significantly impacted by prenatal exposure/insult with sham having the highest radial diffusivity (RD; 4.97 × 10-4 ± 2.20 × 10-5 mm2/s; p < 0.05) and MD (4.41 × 10-4 ± 2.10 × 10-5 mm2/s; p < 0.05) compared to the other groups. The striatum was sensitive to the prenatal exposure/insult, with the axial diffusivity (AD), RD, and MD all significantly increased in the PAE group and decreased in the PI group (p < 0.05). In the corpus callosum, the prenatal exposure/insult significantly decreased the AD (p < 0.05; PAE+PI AD: 5.00 × 10-4 ± 4.60 × 10-5 mm2/s).

conclusionWhile all areas analyzed were impacted by the prenatal insults, the striatum, which consists primarily of efferent pathways, appears more vulnerable to injury compared to the PFC. Additional studies are needed to characterize the impact this may have on function related to these critical brain regions.

Indexed as

Magnetic resonance imagingMedial prefrontal cortexMyelinationPlacental insufficiencyPrenatal alcohol exposure

Identifiers

PMID41237071
PMCPMC12695109

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