Evidence map›Paper›PMID 29472840›Full record

ArticleFrontiers in molecular neuroscience2018

Prenatal Immune Challenge in Mice Leads to Partly Sex-Dependent Behavioral, Microglial, and Molecular Abnormalities Associated with Schizophrenia.

Chin W Hui, Abygaël St-Pierre, Hassan El Hajj, Yvan Remy, Sébastien S Hébert, Giamal N Luheshi, Lalit K Srivastava, Marie-Ève Tremblay

Open access · goldAbstract read
In one paragraph

Article in Frontiers in molecular neuroscience, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 84 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
84citing papers in PubMed, 1 pooled it
9.6field-weighted citation impact, top 1% 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

84 citing papers in PubMed, 1 synthesis or guideline pooled it, 160 citations in OpenAlex.

  1. Pooled it
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  17. Metabolic Control of Microglia.Advances in neurobiology · 2024
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24 more citing papers are in PubMed but not listed here.

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 3 institutions in 1 country.

Chin W HuiAxe Neurosciences, CRCHU de Québec-Université Laval, Québec, QC, Canada.
Abygaël St-PierreAxe Neurosciences, CRCHU de Québec-Université Laval, Québec, QC, Canada.
Hassan El HajjAxe Neurosciences, CRCHU de Québec-Université Laval, Québec, QC, Canada.
Yvan RemyAxe Neurosciences, CRCHU de Québec-Université Laval, Québec, QC, Canada.
Sébastien S HébertAxe Neurosciences, CRCHU de Québec-Université Laval, Québec, QC, Canada.
Giamal N LuheshiDepartment of Psychiatry, Douglas Mental Health University Institute, McGill University, Montréal, QC, Canada.
Lalit K SrivastavaDepartment of Psychiatry, Douglas Mental Health University Institute, McGill University, Montréal, QC, Canada.
Marie-Ève TremblayAxe Neurosciences, CRCHU de Québec-Université Laval, Québec, QC, Canada.
Université Laval · CADouglas Mental Health University Institute · CAMcGill University · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Epidemiological studies revealed that environmental factors comprising prenatal infection are strongly linked to risk for later development of neuropsychiatric disorders such as schizophrenia. Considering strong sex differences in schizophrenia and its increased prevalence in males, we designed a methodological approach to investigate possible sex differences in pathophysiological mechanisms. Prenatal immune challenge was modeled by systemic administration of the viral mimic polyinosinic-polycytidylic acid (Poly I:C) to C57BL/6 mice at embryonic day 9.5. The consequences on behavior, gene expression, and microglia-brain immune cells that are critical for normal development-were characterized in male vs. female offspring at adulthood. The cerebral cortex, hippocampus, and cerebellum, regions where structural and functional alterations were mainly described in schizophrenia patients, were selected for cellular and molecular analyses. Confocal and electron microscopy revealed most pronounced differences in microglial distribution, arborization, cellular stress, and synaptic interactions in the hippocampus of male vs. female offspring exposed to Poly I:C. Sex differences in microglia were also measured under both steady-state and Poly I:C conditions. These microglial alterations were accompanied by behavioral impairment, affecting for instance sensorimotor gating, in males. Consistent with these results, increased expression of genes related to inflammation was measured in cerebral cortex and hippocampus of males challenged with Poly I:C. Overall, these findings suggest that schizophrenia's higher incidence in males might be associated, among other mechanisms, with an increased microglial reactivity to prenatal immune challenges, hence determining disease outcomes into adulthood.

Indexed as

behavior and cognitionelectron microscopygene expressionimmune challengemicrogliamorphology and physiologyschizophreniaultrastructure change

Identifiers

PMID29472840
PMCPMC5809492
OpenAlexW2792302958

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.