Evidence map›Paper›PMID 37113978›Full record

ArticlePNAS nexus2023

Developmental pyrethroid exposure causes a neurodevelopmental disorder phenotype in mice.

Melissa A Curtis, Rohan K Dhamsania, Rachel C Branco, Ji-Dong Guo, Justin Creeden, Kari L Neifer, Carlie A Black, Emily J Winokur, Elissar Andari, Brian G Dias and 4 more

Open access · goldAbstract read
In one paragraph

Article in PNAS nexus, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
8.3field-weighted citation impact, top 3% 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

17 citing papers in PubMed, 21 citations in OpenAlex.

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  10. Microbiome: A Key Regulator of Body-Brain Interactions.Advances in experimental medicine and biology · 2025
    Review
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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

14 authors at 6 institutions in 1 country.

Melissa A CurtisDepartment of Neurosciences, University of Toledo College of Medicine and Life Sciences, USA.
Rohan K DhamsaniaCollege of Arts and Sciences, Emory University, Atlanta, GA 30322, USA.
Rachel C BrancoLaney Graduate School, Emory University, Atlanta, GA 30322, USA.
Ji-Dong GuoDepartment of Psychiatry and Behavioral Sciences, Emory University School of Medicine, Atlanta, GA 30322, USA.
Justin CreedenDepartment of Medicine, University of Toledo College of Medicine and Life Sciences, Toledo, OH 43614, USA.ORCID https://orcid.org/0000-0003-3123-8401
Kari L NeiferDepartment of Neurosciences, University of Toledo College of Medicine and Life Sciences, USA.ORCID https://orcid.org/0000-0002-3691-3851
Carlie A BlackLaney Graduate School, Emory University, Atlanta, GA 30322, USA.
Emily J WinokurCollege of Arts and Sciences, Emory University, Atlanta, GA 30322, USA.
Elissar AndariDepartment of Psychiatry and Behavioral Sciences, Emory University School of Medicine, Atlanta, GA 30322, USA.ORCID https://orcid.org/0000-0002-9745-2745
Brian G DiasDepartment of Psychiatry and Behavioral Sciences, Emory University School of Medicine, Atlanta, GA 30322, USA.ORCID https://orcid.org/0000-0001-9727-4873
Robert C LiuDepartment of Biology, Emory University, Atlanta, GA 30322, USA.ORCID https://orcid.org/0000-0003-2450-8194
Shannon L GourleyDepartment of Pediatrics, Children's Healthcare of Atlanta, Emory University School of Medicine, Atlanta, GA 30322, USA.
Gary W MillerDepartment of Environmental Health, Emory Rollins School of Public Health, Atlanta, GA 30322, USA.ORCID https://orcid.org/0000-0001-8984-1284
James P BurkettDepartment of Neurosciences, University of Toledo College of Medicine and Life Sciences, USA.ORCID https://orcid.org/0000-0002-6357-5499
Emory University · USUniversity of Toledo · USChildren's Hospital of Los Angeles · USColumbia University · USPhiladelphia College of Osteopathic Medicine · USUniversity of Notre Dame · US

Funding

Yerkes National Primate Research Center Role of type-I IFN in regulating COVID-19 induced inflammation and pathogenesisP51OD011132 · OD · EMORY UNIVERSITY · PI Joon Sup Lee · 2012 to 2026
$167.0M
The Impact of Oxytocin on the Neural Representation Social Stimuli P50MH100023 · NIMH · EMORY UNIVERSITY · PI YOUNG, LARRY J · 2013 to 2022
$21.8M
Resubmission of Functional approach to communication sound processing in mouse auditory cortexR01DC008343 · NIDCD · EMORY UNIVERSITY · PI Robert C Liu · 2006 to 2026
$7.2M
Vesicular Modulation of Dopamine Neuron ToxicityR01ES023839 · NIEHS · EMORY UNIVERSITY · PI MILLER, GARY W · 2015 to 2025
$5.0M
Sub-thalamic modulation of learning-related dimensions of PTSD.R01MH120133 · NIMH · EMORY UNIVERSITY · PI DIAS, BRIAN GEORGE · 2019 to 2023
$2.3M
Behavioral and Neurological Effects of Developmental Pyrethroid Exposure in RodentsR00ES027869 · NIEHS · UNIVERSITY OF TOLEDO HEALTH SCI CAMPUS · PI BURKETT, JAMES · 2020 to 2022
$747k
Behavioral and Neurological Effects of Developmental Pyrethroid Exposure in RodentsK99ES027869 · NIEHS · EMORY UNIVERSITY · PI BURKETT, JAMES · 2017 to 2019
$268k
NIDCD NIH HHS R01 DC008343NIEHS NIH HHS K99 ES027869NIEHS NIH HHS R00 ES027869NIEHS NIH HHS R01 ES023839NIH HHS P51 OD011132NIMH NIH HHS P50 MH100023NIMH NIH HHS R01 MH120133
6 · The paper itself

Abstract

Neurodevelopmental disorders (NDDs) are a widespread and growing public health challenge, affecting as many as 17% of children in the United States. Recent epidemiological studies have implicated ambient exposure to pyrethroid pesticides during pregnancy in the risk for NDDs in the unborn child. Using a litter-based, independent discovery-replication cohort design, we exposed mouse dams orally during pregnancy and lactation to the Environmental Protection Agency's reference pyrethroid, deltamethrin, at 3 mg/kg, a concentration well below the benchmark dose used for regulatory guidance. The resulting offspring were tested using behavioral and molecular methods targeting behavioral phenotypes relevant to autism and NDD, as well as changes to the striatal dopamine system. Low-dose developmental exposure to the pyrethroid deltamethrin (DPE) decreased pup vocalizations, increased repetitive behaviors, and impaired both fear conditioning and operant conditioning. Compared with control mice, DPE mice had greater total striatal dopamine, dopamine metabolites, and stimulated dopamine release, but no difference in vesicular dopamine capacity or protein markers of dopamine vesicles. Dopamine transporter protein levels were increased in DPE mice, but not temporal dopamine reuptake. Striatal medium spiny neurons showed changes in electrophysiological properties consistent with a compensatory decrease in neuronal excitability. Combined with previous findings, these results implicate DPE as a direct cause of an NDD-relevant behavioral phenotype and striatal dopamine dysfunction in mice and implicate the cytosolic compartment as the location of excess striatal dopamine.

Indexed as

behavioral toxicologydopamineexposure modelsneurodevelopmental disorderspyrethroid pesticides

Identifiers

PMID37113978
PMCPMC10129348
OpenAlexW4366998649

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.