Evidence map›Paper›PMID 36157343›Full record

ArticleEnvironmental science and ecotechnology2022

Organophosphate esters cause thyroid dysfunction via multiple signaling pathways in zebrafish brain.

Zhenfei Yan, Chenglian Feng, Xiaowei Jin, Fangkun Wang, Cong Liu, Na Li, Yu Qiao, Yingchen Bai, Fengchang Wu, John P Giesy

Abstract read
In one paragraph

Article in Environmental science and ecotechnology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
–field-weighted citation impact
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

12 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. 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
    Article
  6. Review
  7. Article
  8. Review
  9. Article
  10. Review
  11. Article
  12. Review
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.

Zhenfei YanState Key Laboratory of Environmental Criteria and Risk Assessment, Chinese Research Academy of Environmental Sciences, Beijing, 100012, China.
Chenglian FengState Key Laboratory of Environmental Criteria and Risk Assessment, Chinese Research Academy of Environmental Sciences, Beijing, 100012, China.
Xiaowei JinChina National Environmental Monitoring Centre, Beijing, 100012, China.
Fangkun WangDepartment of Preventive Veterinary Medicine, College of Veterinary Medicine, Shandong Agricultural University, Taian, 271018, China.
Cong LiuDepartment of Preventive Veterinary Medicine, College of Veterinary Medicine, Shandong Agricultural University, Taian, 271018, China.
Na LiKey Laboratory of Drinking Water Science and Technology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing, 100085, China.
Yu QiaoState Key Laboratory of Environmental Criteria and Risk Assessment, Chinese Research Academy of Environmental Sciences, Beijing, 100012, China.
Yingchen BaiState Key Laboratory of Environmental Criteria and Risk Assessment, Chinese Research Academy of Environmental Sciences, Beijing, 100012, China.
Fengchang WuState Key Laboratory of Environmental Criteria and Risk Assessment, Chinese Research Academy of Environmental Sciences, Beijing, 100012, China.
John P GiesyDepartment of Veterinary Biomedical Sciences, University of Saskatchewan, Saskatoon, SK, Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Organophosphate esters (OPEs) are widespread in various environmental media, and can disrupt thyroid endocrine signaling pathways. Mechanisms by which OPEs disrupt thyroid hormone (TH) signal transduction are not fully understood. Here, we present in vivo-in vitro-in silico evidence establishing OPEs as environmental THs competitively entering the brain to inhibit growth of zebrafish via multiple signaling pathways. OPEs can bind to transthyretin (TTR) and thyroxine-binding globulin, thereby affecting the transport of TH in the blood, and to the brain by TTR through the blood-brain barrier. When GH3 cells were exposed to OPEs, cell proliferation was significantly inhibited given that OPEs are competitive inhibitors of TH. Cresyl diphenyl phosphate was shown to be an effective antagonist of TH. Chronic exposure to OPEs significantly inhibited the growth of zebrafish by interfering with thyroperoxidase and thyroglobulin to inhibit TH synthesis. Based on comparisons of modulations of gene expression with the Gene Ontology and Kyoto Encyclopedia of Genes and Genomes databases, signaling pathways related to thyroid endocrine functions, such as receptor-ligand binding and regulation of hormone levels, were identified as being affected by exposure to OPEs. Effects were also associated with the biosynthesis and metabolism of lipids, and neuroactive ligand-receptor interactions. These findings provide a comprehensive understanding of the mechanisms by which OPEs disrupt thyroid pathways in zebrafish.

Indexed as

AChE, acetylcholinesteraseandrogen, and steroidogenesisANOVA, analysis of varianceBCF, bioconcentration factorBFR, brominated flame retardantCD-FBS, charcoal-dextran-treated fetal bovine serumCDP, cresyl diphenyl phosphatecga, glycoprotein hormoneCompetitive inhibition assayDEG, differentially expressed geneDKA, β-diketone antibioticDMSO, dimethyl sulfoxideEAS, estrogenFBS, fetal bovine serumGAPDH, glyceraldehyde-3-phosphate dehydrogenaseGO, Gene OntologyHPLC-MS/MS, high-performance liquid chromatograph interfaced with a mass spectrometerHPT, hypothalamic–pituitary–thyroidHS, horse serumKEGG, Kyoto Encyclopedia of Genes and GenomesMAPK, mitogen-activated protein kinaseMolecular docking simulationNIS, Na+/I− symporterOD490, optical densityOPE, organophosphate esterOPFR, organophosphate flame retardantOrganophosphate esterPBDE, polybrominated diphenyl etherPBS, phosphate-buffered salineP/S, penicillin–streptomycinqRT-PCR, quantitative real-time PCRRIC20/50, concentration inhibiting 20%/50%T4, thyroxinTBG, thyroxine-binding globulinTCIPP, tris(2-chloroisopropyl) phosphateTDCIPP-d15, tris(1,3-dichloroisopropyl) phosphate-D15TDCIPP, tris(1,3-dichloro-2-propyl) phosphate (TDCIPP)TG, thyroglobulinTHR, thyroid hormone receptorTH, thyroid hormoneThyroid endocrine functionTIPP, tris(isopropyl) phosphateTPHP, triphenyl phosphateTPO, thyroperoxidaseTranscriptome sequencingTRβ, thyroid hormone receptor βtshβa, thyroid-stimulating hormone beta subunit aTTR, transthyretin

Identifiers

PMID36157343
PMCPMC9500371

What OpenQuestion holds

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LicenceCC BY-NC-ND
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.