Evidence map›Paper›PMID 30413779›Full record

ArticleScientific reports2018

Mammalian Susceptibility to a Neonicotinoid Insecticide after Fetal and Early Postnatal Exposure.

Andrew P Burke, Yosuke Niibori, Hayato Terayama, Masatoshi Ito, Charlotte Pidgeon, Jason Arsenault, Pablo R Camarero, Carolyn L Cummins, Rafael Mateo, Kou Sakabe and 1 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed, 2 pooled it
5.2field-weighted citation impact, top 5% 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

31 citing papers in PubMed, 2 syntheses or guidelines pooled it, 84 citations in OpenAlex.

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  18. Frontiers in physiology · 2023
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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

11 authors at 3 institutions in 3 countries.

Andrew P BurkeDepartment of Pharmaceutical Sciences, Leslie Dan Faculty of Pharmacy, University of Toronto, Toronto, Canada.
Yosuke NiiboriDepartment of Pharmaceutical Sciences, Leslie Dan Faculty of Pharmacy, University of Toronto, Toronto, Canada.
Hayato TerayamaDepartment of Anatomy, Division of Basic Medicine, Tokai University School of Medicine, Kanagawa, 259-1193, Japan.
Masatoshi ItoSupport Center for Medical Research and Education, Tokai University School of Medicine, Kanagawa, 259-1193, Japan.
Charlotte PidgeonDepartment of Pharmaceutical Sciences, Leslie Dan Faculty of Pharmacy, University of Toronto, Toronto, Canada.
Jason ArsenaultDepartment of Pharmaceutical Sciences, Leslie Dan Faculty of Pharmacy, University of Toronto, Toronto, Canada.
Pablo R CamareroInstituto de Investigación en Recursos Cinegéticos (IREC) CSIC-UCLM-JCCM, Ronda de Toledo s/n, 13071, Ciudad Real, Spain.ORCID http://orcid.org/0000-0002-2047-6554
Carolyn L CumminsDepartment of Pharmaceutical Sciences, Leslie Dan Faculty of Pharmacy, University of Toronto, Toronto, Canada.ORCID http://orcid.org/0000-0001-7603-6577
Rafael MateoInstituto de Investigación en Recursos Cinegéticos (IREC) CSIC-UCLM-JCCM, Ronda de Toledo s/n, 13071, Ciudad Real, Spain.
Kou SakabeDepartment of Anatomy, Division of Basic Medicine, Tokai University School of Medicine, Kanagawa, 259-1193, Japan.
David R HampsonDepartment of Pharmaceutical Sciences, Leslie Dan Faculty of Pharmacy, University of Toronto, Toronto, Canada. d.hampson@utoronto.ca.
University of Toronto · CATokai University · JPInstituto de Investigación en Recursos Cinegéticos · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Neonicotinoids have become the most widely used class of insecticides world-wide. Although numerous studies have documented neonicotinoid toxicity in bees and other insects, the effects of exposure during early development in mammals remain largely unexplored. We assessed the effects of the neonicotinoid imidacloprid (IMI) in adult male and female mice after in utero and early postnatal exposure. Pregnant mice were infused with IMI (0.5 mg/kg/day) from gestational day 4 to the end of nursing at postnatal day 21. The young adult offspring were studied in a series of biochemical and behavioral tests. To assess reproducibility, the behavioral analyses were conducted in three separate studies using multiple exposed litters. Exposure to IMI reduced fecundity, and in adult offspring, decreased body weight in male but not female pups. Offspring from IMI-treated mothers displayed lower triglycerides, elevated motor activity, enhanced social dominance, reduced depressive-like behavior, and a diminution in social aggression compared to vehicle treated controls. Low levels of IMI were detected in the brains and livers of the treated mothers, while trace levels were detected in some offspring. Our results demonstrate that transient exposure to a neonicotinoid over the early developmental period induces long-lasting changes in behavior and brain function in mice.

Indexed as

AnimalsBehavior, AnimalBody WeightBrainFemaleFertilityInsecticidesMaleMiceNeonicotinoidsPregnancyPrenatal Exposure Delayed EffectsInsecticidesNeonicotinoids

Identifiers

PMID30413779
PMCPMC6226530
OpenAlexW2900212218

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.