Evidence map›Paper›PMID 26743178›Full record

ArticleScientific reports2016

Acute Exposure to Tris(1,3-dichloro-2-propyl) Phosphate (TDCIPP) Causes Hepatic Inflammation and Leads to Hepatotoxicity in Zebrafish.

Chunsheng Liu, Guanyong Su, John P Giesy, Robert J Letcher, Guangyu Li, Ira Agrawal, Jing Li, Liqin Yu, Jianghua Wang, Zhiyuan Gong

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
5.3field-weighted citation impact, top 4% 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

20 citing papers in PubMed, 70 citations in OpenAlex.

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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 5 institutions in 4 countries.

Chunsheng LiuCollege of Fisheries, Huazhong Agricultural University, Wuhan 430070, China.
Guanyong SuDepartment of Chemistry, Carleton University, Ottawa, Ontario K1S 5B6, Canada.
John P GiesyState Key Laboratory of Pollution Control and Resource Reuse, School of the Environment, Nanjing University, Nanjing 210023, China.
Robert J LetcherDepartment of Chemistry, Carleton University, Ottawa, Ontario K1S 5B6, Canada.
Guangyu LiCollege of Fisheries, Huazhong Agricultural University, Wuhan 430070, China.
Ira AgrawalDepartment of Biological Sciences, National University of Singapore, Singapore 117543, Singapore.
Jing LiCollege of Fisheries, Huazhong Agricultural University, Wuhan 430070, China.
Liqin YuCollege of Fisheries, Huazhong Agricultural University, Wuhan 430070, China.
Jianghua WangCollege of Fisheries, Huazhong Agricultural University, Wuhan 430070, China.
Zhiyuan GongDepartment of Biological Sciences, National University of Singapore, Singapore 117543, Singapore.
Huazhong Agricultural University · CNNational University of Singapore · SGCarleton University · CAState Key Laboratory of Pollution Control and Resource Reuse · CNUniversity of Saskatchewan · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tris(1,3-dichloro-2-propyl) phosphate (TDCIPP) has been frequently detected in environmental media and has adverse health effect on wildlife and humans. It has been implicated to have hepatotoxicity, but its molecular mechanisms remain unclear. In the present study, adult male zebrafish were exposed to TDCIPP and global hepatic gene expression was examined by RNA-Seq and RT-qPCR in order to understand the molecular mechanisms of TDCIPP-induced hepatotoxicity. Our results indicated that TDCIPP exposure significantly up-regulated the expression of genes involved in endoplasmic reticulum stress and Toll-like receptor (TLR) pathway, implying an inflammatory response, which was supported by up-regulation of inflammation-related biomaker genes. Hepatic inflammation was further confirmed by histological observation of increase of infiltrated neutrophils and direct observation of liver recruitment of neutrophils labeled with Ds-Red fluorescent protein of Tg(lysC:DsRed) zebrafish upon TDCIPP exposure. To further characterize the hepatotoxicity of TDCIPP, the expression of hepatotoxicity biomarker genes, liver histopathology and morphology were examined. The exposure to TDCIPP significantly up-regulated the expression of several biomarker genes for hepatotoxicity (gck, gsr and nqo1) and caused hepatic vacuolization and apoptosis as well as increase of the liver size. Collectively, our results suggest that exposure to TDCIPP induces hepatic inflammation and leads to hepatotoxicity in zebrafish.

Indexed as

AnimalsChemical and Drug Induced Liver InjuryEmbryo, NonmammalianEndoplasmic Reticulum StressFlame RetardantsGene Expression Regulation, DevelopmentalGenes, ReporterGerminal Center KinasesInflammationLarvaLiverLuminescent ProteinsMaleNAD(P)H Dehydrogenase (Quinone)Neutrophil InfiltrationNeutrophilsFlame Retardantsfluorescent protein 583Germinal Center KinasesLuminescent ProteinsNAD(P)H Dehydrogenase (Quinone)Organophosphorus CompoundsProtein Serine-Threonine KinasesToll-Like Receptorstris(1,3-dichloro-2-propyl)phosphateWater Pollutants, ChemicalZebrafish Proteins

Identifiers

PMID26743178
PMCPMC4705469
OpenAlexW2227470438

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.