Evidence map›Paper›PMID 40744256›Full record

ArticleNeurotoxicology2025

Parental preconceptual α-cypermethrin exposure alters embryonic brain transcriptomics in mice: Implications for autism spectrum disorder and stress vulnerability.

Benjamin Hing, Robert Taylor, Samuel Eliasen, Hanna E Stevens

Abstract read
In one paragraph

Article in Neurotoxicology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. Article
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

4 authors.

Benjamin HingDepartment of Molecular Physiology and Biophysics, Carver College of Medicine, The University of Iowa, Iowa City, IA, USA. Electronic address: benjamin-hing@uiowa.edu.
Robert TaylorDepartment of Psychiatry, Carver College of Medicine, The University of Iowa, Iowa City, IA, USA.
Samuel EliasenDepartment of Psychiatry, Carver College of Medicine, The University of Iowa, Iowa City, IA, USA.
Hanna E StevensDepartment of Psychiatry, Carver College of Medicine, The University of Iowa, Iowa City, IA, USA.

Funding

Pulmonary Toxicology Facility CoreP30ES005605 · NIEHS · UNIVERSITY OF IOWA · PI Jong Sung Kim · 1990 to 2026
$40.5M
University of Iowa Hawkeye Intellectual and Developmental Disabilities Research Center (Hawk-IDDRC)P50HD103556 · NICHD · UNIVERSITY OF IOWA · PI EDWIN TED G. ABEL, Lane Strathearn · 2021 to 2026
$8.5M
Research Training for Medical Students & Physician-Scientists in Child PsychiatryR25MH077823 · NIMH · YALE UNIVERSITY · PI ANDRES S MARTIN · 2006 to 2026
$4.0M
Adolescent Insecticide Exposure and ADHD Risk: Mechanisms of Immediate Effects and Long-term VulnerabilityR01ES035696 · NIEHS · UNIVERSITY OF IOWA · PI HANNA E STEVENS · 2024 to 2026
$1.5M
NICHD NIH HHS P50 HD103556NIEHS NIH HHS P30 ES005605NIEHS NIH HHS R01 ES035696NIMH NIH HHS R25 MH077823
6 · The paper itself

Abstract

Pyrethroid insecticides are widely used in agriculture and households, and their exposure can affect neurodevelopment. Few studies have evaluated how preconception parental exposure could also affect this process. To address this knowledge gap, adult C57Bl6/J mice were gavaged daily with α-cypermethrin at a human relevant low (0.3 mg/kg) or high (10 mg/kg) dose in corn oil for four weeks prior to conception. Offspring embryonic day 16 dorsal forebrain was extracted for transcriptomic analysis. In offspring forebrains of exposed compared to unexposed parents, there was increasing number of differentially expressed genes (DEGs) from paternal (least) to maternal to both parent exposure (most). A dose dependent effect was observed in offspring forebrain for paternal and maternal preconceptual exposures. Maternal and both parent exposures led to upregulated genes in offspring brain for biological processes involved in translation with predicted activation of EIF4E, a gene associated with autism. In contrast, paternal exposure upregulated cell cycle related DNA damage signaling processes. After any parent exposure, there was upregulation of biological processes involved in mitochondria function and oxidative stress and a downregulation of neuronal and synaptic processes with predicted inhibition of BDNF signaling. Weighted gene correlation network analysis identified modules associated with different parent exposures that were over-represented with DEGs and had similar functional signatures as DEG-related pathways. Importantly, DEGs in offspring forebrain after any parent exposure were over-represented with genes related to autism spectrum disorder (ASD) and stress vulnerability. The study highlights the potential contribution of preconception parental pyrethroid exposure to aberrant brain functioning.

Indexed as

Gene Expression Regulation, DevelopmentalInsecticidesPrenatal Exposure Delayed EffectsPyrethrinsTranscriptomeAnimalsAutism Spectrum DisorderBrainBrain-Derived Neurotrophic FactorDNA DamageDose-Response Relationship, DrugEukaryotic Initiation Factor-4EFemaleMaleMaternal ExposureMiceBdnf protein, mouseBrain-Derived Neurotrophic FactorcypermethrineIF4E protein, mouseEukaryotic Initiation Factor-4EInsecticidesPyrethrinsAutism Spectrum DisorderCypermethrinNeurodevelopmentPesticidesStress vulnerabilityTranscriptomics

Identifiers

PMID40744256
PMCPMC12501635

What Socratic holds

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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 Socratic graph.