Evidence map›Paper›PMID 32243540›Full record

ArticleToxicological sciences : an official journal of the Society of Toxicology2020

Effects of Prenatal Exposure to a Mixture of Organophosphate Flame Retardants on Placental Gene Expression and Serotonergic Innervation in the Fetal Rat Brain.

Kylie D Rock, Genevieve St Armour, Brian Horman, Allison Phillips, Matthew Ruis, Allison K Stewart, Dereje Jima, David C Muddiman, Heather M Stapleton, Heather B Patisaul

Open access · greenAbstract read
In one paragraph

Article in Toxicological sciences : an official journal of the Society of Toxicology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
3.6field-weighted citation impact, top 6% 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

36 citing papers in PubMed, 65 citations in OpenAlex.

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  9. Impact of exposure to a mixture of organophosphate esters on the adrenal glands of Sprague Dawley rats.Toxicological sciences : an official journal of the Society of Toxicology · 2025
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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

10 authors at 2 institutions in 1 country.

Kylie D RockDepartment of Biological Sciences, North Carolina State University, Raleigh, North Carolina 27619.
Genevieve St ArmourDepartment of Biological Sciences, North Carolina State University, Raleigh, North Carolina 27619.
Brian HormanDepartment of Biological Sciences, North Carolina State University, Raleigh, North Carolina 27619.
Allison PhillipsNicholas School of the Environment, Duke University, Durham, North Carolina 27708.
Matthew RuisNicholas School of the Environment, Duke University, Durham, North Carolina 27708.
Allison K StewartMolecular Education, Technology, and Research Innovation Center, North Carolina State University, Raleigh, North Carolina 27695.
Dereje JimaCenter for Human Health and the Environment, North Carolina State University, Raleigh, North Carolina 27695.
David C MuddimanMolecular Education, Technology, and Research Innovation Center, North Carolina State University, Raleigh, North Carolina 27695.
Heather M StapletonNicholas School of the Environment, Duke University, Durham, North Carolina 27708.
Heather B PatisaulDepartment of Biological Sciences, North Carolina State University, Raleigh, North Carolina 27619.
North Carolina State University · USDuke University · US

Funding

Translational Research Support CoreP30ES025128 · NIEHS · NORTH CAROLINA STATE UNIVERSITY RALEIGH · PI Sue Fenton · 2015 to 2026
$18.3M
TRAINING IN BIOCHEMICAL AND ENVIRONMENTAL TOXICOLOGYT32ES007046 · NIEHS · NORTH CAROLINA STATE UNIVERSITY RALEIGH · PI Seth William Kullman · 1985 to 2026
$5.1M
Children's Exposure to Flame Retardants: Effects on Thyroid Hormone RegulationR01ES016099 · NIEHS · DUKE UNIVERSITY · PI STAPLETON, HEATHER M · 2008 to 2017
$5.0M
Development and Application of New Ionization Methods for Biological Mass SpectrometryR01GM087964 · NIGMS · NORTH CAROLINA STATE UNIVERSITY RALEIGH · PI MUDDIMAN, DAVID C. · 2010 to 2025
$4.7M
The placenta: a novel target of sex specific neurotoxicity by fire retardantsR01ES028110 · NIEHS · NORTH CAROLINA STATE UNIVERSITY RALEIGH · PI MEITZEN, JOHN · 2017 to 2022
$2.4M
Toxicokinetics and Metabolic Disrupting Actions of the Flame Retardant Mixture FMR56ES022957 · NIEHS · NORTH CAROLINA STATE UNIVERSITY RALEIGH · PI BELCHER, SCOTT M, PATISAUL, HEATHER B · 2014 to 2014
$300k
NIEHS NIH HHS P30 ES025128NIEHS NIH HHS R01 ES016099NIEHS NIH HHS R01 ES028110NIEHS NIH HHS R56 ES022957NIEHS NIH HHS T32 ES007046NIGMS NIH HHS R01 GM087964
6 · The paper itself

Abstract

There is a growing need to understand the potential neurotoxicity of organophosphate flame retardants (OPFRs) and plasticizers because use and, consequently, human exposure, is rapidly expanding. We have previously shown in rats that developmental exposure to the commercial flame retardant mixture Firemaster 550 (FM 550), which contains OPFRs, results in sex-specific behavioral effects, and identified the placenta as a potential target of toxicity. The placenta is a critical coordinator of fetal growth and neurodevelopment, and a source of neurotransmitters for the developing brain. We have shown in rats and humans that flame retardants accumulate in placental tissue, and induce functional changes, including altered neurotransmitter production. Here, we sought to establish if OPFRs (triphenyl phosphate and a mixture of isopropylated triarylphosphate isomers) alter placental function and fetal forebrain development, with disruption of tryptophan metabolism as a primary pathway of interest. Wistar rat dams were orally exposed to OPFRs (0, 500, 1000, or 2000 μg/day) or a serotonin (5-HT) agonist 5-methoxytryptamine for 14 days during gestation and placenta and fetal forebrain tissues collected for analysis by transcriptomics and metabolomics. Relative abundance of genes responsible for the transport and synthesis of placental 5-HT were disrupted, and multiple neuroactive metabolites in the 5-HT and kynurenine metabolic pathways were upregulated. In addition, 5-HTergic projections were significantly longer in the fetal forebrains of exposed males. These findings suggest that OPFRs have the potential to impact the 5-HTergic system in the fetal forebrain by disrupting placental tryptophan metabolism.

Indexed as

Prenatal Exposure Delayed EffectsAnimalsBrainFemaleFetal DevelopmentFetusFlame RetardantsGene ExpressionHumansMaleOrganophosphatesOrganophosphorus CompoundsPlacentaPlasticizersPolybrominated BiphenylsPregnancyFiremaster 550Flame RetardantsOrganophosphatesOrganophosphorus CompoundsPlasticizersPolybrominated BiphenylsSerotonintriphenyl phosphatedevelopmentaldevelopmental/teratologydevelopmental toxicityendocrine disruptorsendocrine toxicologyflame retardantsmetabolomeneurotoxicityneurotoxicologyneurotransmitterprenatalreproductive and developmental toxicology

Identifiers

PMID32243540
PMCPMC7357193
OpenAlexW3014358433

What OpenQuestion holds

Textmetadata
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.