Evidence map›Paper›PMID 31872887›Full record

ArticleAlcoholism, clinical and experimental research2020

Prenatal Ethanol Exposure and Postnatal Environmental Intervention Alter Dopaminergic Neuron and Microglia Morphology in the Ventral Tegmental Area During Adulthood.

Claudia I Aghaie, Kathryn A Hausknecht, Ruixiang Wang, Parisa Halaji Dezfuli, Samir Haj-Dahmane, Cynthia J M Kane, Wade J Sigurdson, Roh-Yu Shen

Open access · greenAbstract read
In one paragraph

Article in Alcoholism, clinical and experimental research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
5.5field-weighted citation impact, top 4% 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

23 citing papers in PubMed, 27 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

8 authors at 2 institutions in 1 country.

Claudia I AghaieDepartment of Pathology and Anatomical Sciences, University at Buffalo, Buffalo, New York.
Kathryn A HausknechtDepartment of Pharmacology and Toxicology, University at Buffalo, Buffalo, New York.ORCID 0000-0003-2748-364X
Ruixiang WangDepartment of Pharmacology and Toxicology, University at Buffalo, Buffalo, New York.ORCID 0000-0003-0316-0600
Parisa Halaji DezfuliDepartment of Pharmacology and Toxicology, University at Buffalo, Buffalo, New York.
Samir Haj-DahmaneDepartment of Pharmacology and Toxicology, University at Buffalo, Buffalo, New York.
Cynthia J M KaneDepartment of Neurobiology and Developmental Sciences, College of Medicine, the University of Arkansas for Medical Sciences, Little Rock, Arkansas.
Wade J SigurdsonDepartment of Pathology and Anatomical Sciences, University at Buffalo, Buffalo, New York.
Roh-Yu ShenDepartment of Pathology and Anatomical Sciences, University at Buffalo, Buffalo, New York.
University at Buffalo, State University of New York · USUniversity of Arkansas for Medical Sciences · US

Funding

Addiction Propensity After Prenatal Ethanol ExposureR01AA019482 · NIAAA · STATE UNIVERSITY OF NEW YORK AT BUFFALO · PI SHEN, ROH-YU · 2011 to 2015
$1.7M
DOPAMINE FUNCTION AFTER PRENATAL ETHANOL EXPOSURER01AA012435 · NIAAA · STATE UNIVERSITY OF NEW YORK AT BUFFALO · PI SHEN, ROH-YU · 1999 to 2008
$1.6M
NIAAA NIH HHS AA12435NIAAA NIH HHS R01 AA012435NIAAA NIH HHS R01 AA019482
6 · The paper itself

Abstract

backgroundPrenatal ethanol exposure (PE) impairs midbrain dopaminergic (DA) neuron function, which might contribute to various cognitive and behavioral deficits, including attention deficits and increased addiction risk, often observed in individuals with fetal alcohol spectrum disorders. Currently, the underlying mechanisms for PE-induced deficits are unclear. PE could lead to neuroinflammation by activating microglia, which play an important role in synaptic function. In the present study, we investigated PE effects on microglial activation and DA neuron density and morphology in the ventral tegmental area (VTA). Since postnatal environmental enrichment can reduce neuroinflammation and ameliorate several PE-induced behavioral deficits, we examined if a postnatal environmental intervention strategy using neonatal handling and postweaning complex housing could reverse PE effects on VTA DA neurons and microglia.

methodsPregnant rats received 0 or 6 g/kg/d ethanol by 2 intragastric intubations on gestation days 8 to 20. After birth, rats were reared in the standard laboratory or enriched condition. Male adult rats (8 to 12 weeks old) were used for immunocytochemistry.

resultsThe results showed that PE decreased VTA DA neuron body size in standardly housed rats. Moreover, there was a significant decrease in numbers of VTA microglial branches and junctions in PE rats, suggesting morphological activation of microglia and possible neuroinflammation. The PE effects on microglia were normalized by postnatal environmental intervention, which also decreased the numbers of microglial branches and junctions in control animals, possibly via reduced stress.

conclusionsOur findings show an association between PE-induced morphological activation of microglia and impaired DA neuron morphology in the VTA. Importantly, postnatal environmental intervention rescues possible PE-induced microglial activation. These data support that environmental intervention can be effective in ameliorating cognitive and behavioral deficits associated with VTA DA neuron dysfunctions, such as attention deficits and increased addiction risk.

Indexed as

EnvironmentAge FactorsAnimalsAnimals, NewbornDopaminergic NeuronsEthanolFemaleHousing, AnimalMaleMicrogliaPregnancyPrenatal Exposure Delayed EffectsRatsRats, Sprague-DawleyVentral Tegmental AreaEthanolDopamineEnvironmental EnrichmentFetal Alcohol Spectrum DisordersMicrogliaVentral Tegmental Area

Identifiers

PMID31872887
PMCPMC7153307
OpenAlexW2998079949

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.