Evidence map›Paper›PMID 37146889›Full record

ArticleToxicology and applied pharmacology2023

Benzo[a]pyrene-induced multigenerational changes in gene expression, behavior, and DNA methylation are primarily influenced by paternal exposure.

Z Pandelides, M C Sturgis, C Thornton, N Aluru, K L Willett

Open access · greenAbstract read
In one paragraph

Article in Toxicology and applied pharmacology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

5 citing papers in PubMed, 14 citations in OpenAlex.

  1. Position-specific methyl substitution on benzo[a]pyrene drives AHR-dependent fin duplication in zebrafish.Toxicological sciences : an official journal of the Society of Toxicology · 2026
    Article
  2. Article
  3. Article
  4. Article
  5. A Di-Rhamnolipid (RhaBioFactors (Oxford, England)
    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

5 authors at 2 institutions in 1 country.

Z PandelidesDepartment of BioMolecular Sciences, School of Pharmacy, University of Mississippi, University, MS 38677, United States of America.
M C SturgisDepartment of BioMolecular Sciences, School of Pharmacy, University of Mississippi, University, MS 38677, United States of America.
C ThorntonDepartment of BioMolecular Sciences, School of Pharmacy, University of Mississippi, University, MS 38677, United States of America.
N AluruBiology Department, Woods Hole Oceanographic Institution and Woods Hole Center for Oceans and Human Health, Woods Hole, MA 02543, United States of America.
K L WillettDepartment of BioMolecular Sciences, School of Pharmacy, University of Mississippi, University, MS 38677, United States of America. Electronic address: kwillett@olemiss.edu.
University of Mississippi · USWoods Hole Oceanographic Institution · US

Funding

Mechanisms of developmental and reproductive toxicity from preconceptional BaP exposure - Summer Research Experiences for Students (Admin Supp)R21ES030154 · NIEHS · UNIVERSITY OF MISSISSIPPI · PI WILLETT, KRISTINE L · 2019 to 2020
$422k
Development of a fish model for epigenetic & multigenerational contaminant effectR21ES019940 · NIEHS · UNIVERSITY OF MISSISSIPPI · PI WILLETT, KRISTINE L · 2011 to 2012
$385k
NIEHS NIH HHS R21 ES019940NIEHS NIH HHS R21 ES030154
6 · The paper itself

Abstract

Benzo[a]pyrene (BaP), a polycyclic aromatic hydrocarbon (PAH), is implicated in many developmental and behavioral adverse outcomes in offspring of exposed parents. The objective of this study was to investigate sex-dependent multigenerational effects of preconceptional effects of BaP exposure. Adult wild-type (5D) zebrafish were fed 708 μg BaP/g diet (measured) at a rate of 1% body weight twice/day (14 μg BaP/g fish/day) for 21 days. Fish were spawned using a crossover design, and parental (F0) behavior and reproductive indexes were measured. In offspring, behavioral effects were measured at 96 h post fertilization (hpf) in F1 & F2 larvae, and again when F1s were adults. Compared to controls, there was no significant effect on F0 adult behavior immediately following exposure, but locomotor activity was significantly increased in F1 adults of both sexes. Larval behavior (96 hpf, photomotor response assay) was significantly altered in both the F1 and F2 generations. To assess molecular changes associated with BaP exposure, we conducted transcriptome and DNA methylation profiling in F0 gametes (sperm and eggs) and F1 embryos (10 hpf) from all four crosses. Embryos resulting from the BaP male and control female cross had the most differentially expressed genes (DEGs) and differentially methylated regions (DMRs). Some DMRs were associated with genes encoding chromatin modifying enzymes suggesting regulation of chromatin conformation by DNA methylation. Overall, these results suggest that parental dietary BaP exposure significantly contributes to the multigenerational adverse outcomes.

Indexed as

DNA MethylationPaternal ExposureAnimalsBenzo(a)pyreneCross-Over StudiesFemaleGene ExpressionMaleSemenZebrafishBenzo(a)pyreneBehaviorBenzo[a]PyreneDNA MethylationMultigenerationalPAHRNAseq

Identifiers

PMID37146889
PMCPMC11589888
OpenAlexW4367838077

What OpenQuestion 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 OpenQuestion graph.