Evidence map›Paper›PMID 38953493›Full record

ArticleACS chemical neuroscience2024

Astrocyte Mitochondria Are a Sensitive Target of PCB52 and its Human-Relevant Metabolites.

Neha Paranjape, Stefan Strack, Hans-Joachim Lehmler, Jonathan A Doorn

Abstract read
In one paragraph

Article in ACS chemical neuroscience, 2024. 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.

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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

4 authors.

Neha ParanjapeDepartment of Pharmaceutical Sciences & Experimental Therapeutics, College of Pharmacy, University of Iowa, Iowa City, Iowa 52242, United States.ORCID 0000-0001-7788-0497
Stefan StrackDepartment of Neuroscience and Pharmacology, University of Iowa Carver College of Medicine, Iowa City, Iowa 52242, United States.
Hans-Joachim LehmlerDepartment of Occupational and Environmental Health, College of Public Health, University of Iowa, Iowa City, Iowa 52242, United States.ORCID 0000-0001-9163-927X
Jonathan A DoornDepartment of Pharmaceutical Sciences & Experimental Therapeutics, College of Pharmacy, University of Iowa, Iowa City, Iowa 52242, United States.ORCID 0000-0001-9646-9871

Funding

Training CoreP42ES013661 · NIEHS · UNIVERSITY OF IOWA · PI HANS-JOACHIM LEHMLER · 2006 to 2026
$60.3M
Pulmonary Toxicology Facility CoreP30ES005605 · NIEHS · UNIVERSITY OF IOWA · PI Jong Sung Kim · 1990 to 2026
$40.5M
Targeting Mitochondrial Fission for Neuroprotection in Diabetic NeuropathyR01DK116624 · NIDDK · UNIVERSITY OF IOWA · PI STRACK, STEFAN, USACHEV, YURIY M · 2018 to 2021
$2.1M
Pesticide-Mediated Generation of a Toxic Neurotransmitter MetaboliteR01ES029035 · NIEHS · UNIVERSITY OF IOWA · PI DOORN, JONATHAN A · 2018 to 2022
$1.9M
Interplay between tau and PKA condensates in ADRDR21AG080472 · NIA · UNIVERSITY OF IOWA · PI STRACK, STEFAN, TAYLOR, SUSAN S. · 2023 to 2024
$559k
NIA NIH HHS R21 AG080472NIDDK NIH HHS R01 DK116624NIEHS NIH HHS P30 ES005605NIEHS NIH HHS P42 ES013661NIEHS NIH HHS R01 ES029035
6 · The paper itself

Abstract

Polychlorinated biphenyls (PCBs) are industrial chemicals that are ubiquitously found in the environment. Exposure to these compounds has been associated with neurotoxic outcomes; however, the underlying mechanisms for such outcomes remain to be fully understood. Recent studies have shown that astrocytes, the most abundant glial cell type in the brain, are susceptible to PCB exposure as well as exposure to human-relevant metabolites of PCBs. Astrocytes are critical for maintaining healthy brain function due to their unique functional attributes and positioning within the neuronal networks in the brain. In this study, we assessed the toxicity of PCB52, one of the most abundantly found PCB congeners in outdoor and indoor air, and two of its human-relevant metabolites, on astrocyte mitochondria. We exposed C6 cells, an astrocyte cell line, to PCB52 or its human-relevant metabolites and found that all the compounds showed increased toxicity in galactose-containing media compared to that in the glucose-containing media, indicating the involvement of mitochondria in observed toxicity. Additionally, we also found increased oxidative stress upon exposure to PCB52 metabolites. All three compounds caused a loss of mitochondrial membrane potential, distinct changes in the mitochondrial structure, and impaired mitochondrial function. The hydroxylated metabolite 4-OH-PCB52 likely functions as an uncoupler of mitochondria. This is the first study to report the adverse effects of exposure to PCB52 and its human-relevant metabolites on the mitochondrial structure and function in astrocytes.

Indexed as

AstrocytesMitochondriaPolychlorinated BiphenylsAnimalsCell LineHumansMembrane Potential, MitochondrialOxidative StressRatsPolychlorinated BiphenylsastrocytesmechanismsmitochondrianeurotoxicityPCB metabolitespolychlorinated biphenyls

Identifiers

PMID38953493
PMCPMC11311133

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Registered trials

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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.