Evidence map›Paper›PMID 25659769›Full record

ArticleToxicology in vitro : an international journal published in association with BIBRA2015

Effect of omega-3 fatty acid oxidation products on the cellular and mitochondrial toxicity of BDE 47.

Andrew Yeh, Shane E Kruse, David J Marcinek, Evan P Gallagher

Abstract read
In one paragraph

Article in Toxicology in vitro : an international journal published in association with BIBRA, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Polybrominated diphenyl ethers in the environment: a wake-up call for concerted action in India.Environmental science and pollution research international · 2021
    Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
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

4 authors.

Andrew YehDepartment of Environmental and Occupational Health Sciences, University of Washington, Seattle, WA 98105-6099, United States.
Shane E KruseDepartment of Radiology, University of Washington Medical School, Seattle, WA 98195, United States.
David J MarcinekDepartment of Radiology, University of Washington Medical School, Seattle, WA 98195, United States.
Evan P GallagherDepartment of Environmental and Occupational Health Sciences, University of Washington, Seattle, WA 98105-6099, United States. Electronic address: evang3@u.washington.edu.

Funding

WILDLIFE BIOMARKER APPLICATIONS TO REMEDIATION DECISION MAKINGP42ES004696 · NIEHS · UNIVERSITY OF WASHINGTON · PI FURLONG, CLEMENT EUGENE · 1987 to 2021
$51.2M
Environmetal Pathology/Toxicology Training ProgramT32ES007032 · NIEHS · UNIVERSITY OF WASHINGTON · PI FAUSTMAN, ELAINE M, ROSENFELD, MICHAEL E · 1985 to 2023
$10.7M
Translational Center for In Vivo Mitochondrial MedicineRC2AG036606 · NIA · UNIVERSITY OF WASHINGTON · PI CONLEY, KEVIN E, MARCINEK, DAVID J. · 2009 to 2010
$1.5M
NIA NIH HHS RC2 AG036606NIEHS NIH HHS P42 ES004696NIEHS NIH HHS P42ES004696NIEHS NIH HHS T32 ES007032
6 · The paper itself

Abstract

High levels of the flame retardant 2,2',4,4'-tetrabromodiphenyl ether (BDE 47) have been detected in Pacific salmon sampled near urban areas, raising concern over the safety of salmon consumption. However, salmon fillets also contain the antioxidants eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA), whose oxidation products induce cellular antioxidant responses. Because oxidative stress is a mechanism of BDE 47 toxicity, we hypothesized that oxidized EPA and DHA can ameliorate the cellular and mitochondrial toxicity of BDE 47. HepG2 cells were treated with a mixture of oxidized EPA and DHA (oxEPA/oxDHA) at a ratio relevant to salmon consumption (1.5/1 oxEPA/oxDHA) followed by exposure to 100 μM BDE 47. Pretreatment with oxEPA/oxDHA for 12 h prior to BDE 47 exposure prevented BDE 47-mediated depletion of glutathione, and increased expression of antioxidant response genes. oxEPA/oxDHA also reduced the level of reactive oxygen species production by BDE 47. The oxEPA/oxDHA antioxidant responses were associated with partial protection against BDE 47-induced loss of viability and also mitochondrial membrane potential. Mitochondrial electron transport system functional analysis revealed extensive inhibition of State 3 respiration and maximum respiratory capacity by BDE 47 were partially reversed by oxEPA/oxDHA. Our findings indicate that the antioxidant effects of oxEPA/oxDHA protect against short exposures to BDE 47, including a protective role of these compounds on maintaining cellular and mitochondrial function.

Indexed as

Cell Line, TumorElectron TransportFatty Acids, Omega-3Flame RetardantsGlutathioneHalogenated Diphenyl EthersHumansMembrane Potential, MitochondrialMitochondriaOxidation-ReductionOxidative StressReactive Oxygen Species2,2',4,4'-tetrabromodiphenyl etherFatty Acids, Omega-3Flame RetardantsGlutathioneHalogenated Diphenyl EthersReactive Oxygen SpeciesBDE 47MitochondriaOmega-3 polyunsaturated fatty acidsOxidative stressPBDESalmon

Identifiers

PMID25659769
PMCPMC4479582

What OpenQuestion holds

Textmetadata
LicenceTDM
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.