Combining transcriptomics and metabolomics to assess neurodevelopmental alteration caused by in utero exposure of mice to three putative thyroid hormone system disruptors

Gestating mice were exposed to three chemicals, tetrabromo-bisphenol A (TBBPA; 2 mg/kg/day), amitrole (25 and 50 mg/kg/day) and pyraclostrobin (0.4 and 2 mg/kg/day) to assess their capacity to act as thyroid hormone disruptors and compromise neurodevelopment. Propyl-thio-uracyl, a known pharmacological inhibitor of thyroid gland secretion, was used at both high and low dose as a reference thyroid hormone system disruptor (1 ppm, 1500 ppm). A combination of plasma metabolomics and striatum transcriptomics revealed the induced change in pups at the postnatal stages. Although the underlying mechanism is unlikely to involve thyroid hormone disruption, these chemicals had a detectable effect on pups' neurodevelopment.

Authors

Institutions

Publication Details

Journal
Toxicology
Published
2024-08-11
DOI
https://doi.org/10.1016/j.tox.2024.153905
Citations
3
Primary Topic
Birth, Development, and Health
Type
article
Field-Weighted Citation Impact
3.33

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Combining transcriptomics and metabolomics to assess neurodevelopmental alteration caused by in utero exposure of mice to three putative thyroid hormone system disruptors

Rikke Poulsen, Martin Hansen, Romain Guyot, Frédéric Flamant et al.
3 citations
Toxicology
Birth, Development, and Health
3.33
article

Combining transcriptomics and metabolomics to assess neurodevelopmental alteration caused by in utero exposure of mice to three putative thyroid hormone system disruptors

Rikke Poulsen, Martin Hansen, Romain Guyot, Frédéric Flamant, Yanis Zekri
article en
3 citations

Abstract

Gestating mice were exposed to three chemicals, tetrabromo-bisphenol A (TBBPA; 2 mg/kg/day), amitrole (25 and 50 mg/kg/day) and pyraclostrobin (0.4 and 2 mg/kg/day) to assess their capacity to act as thyroid hormone disruptors and compromise neurodevelopment. Propyl-thio-uracyl, a known pharmacological inhibitor of thyroid gland secretion, was used at both high and low dose as a reference thyroid hormone system disruptor (1 ppm, 1500 ppm). A combination of plasma metabolomics and striatum transcriptomics revealed the induced change in pups at the postnatal stages. Although the underlying mechanism is unlikely to involve thyroid hormone disruption, these chemicals had a detectable effect on pups' neurodevelopment.

ToxicologyVol. 508
École Normale Supérieure de Lyon (FR), Centre National de la Recherche Scientifique (FR), Aarhus University (DK), University of Victoria (CA), The Netherlands Cancer Institute (NL), Institut National de Recherche pour l'Agriculture, l'Alimentation et l'Environnement (FR), Institut de Génomique Fonctionnelle de Lyon (FR)
Aarhus Universitet, European Commission, Aarhus Universitets Forskningsfond, Carlsbergfondet, Horizon 2020 Framework Programme, Horizon 2020, FP7 Coordination of Research Activities
Zero hunger
Openalex Percentile: Top 8%
Birth, Development, and Health
3.33
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.

Combining transcriptomics and metabolomics to assess neurodevelopmental alteration caused by in utero exposure of mice to three putative thyroid hormone system disruptors — Rikke Poulsen, Martin Hansen, et al. · Toxicology (2024) | TGRS Research Map | TGRS