Evidence map›Paper›PMID 34265337›Full record

ArticleNeurotoxicology2021

Polychlorinated biphenyls induce oxidative stress and metabolic responses in astrocytes.

Mondona S McCann, Harvey R Fernandez, Sarah A Flowers, Kathleen A Maguire-Zeiss

Open access · hybridAbstract read
In one paragraph

Article in Neurotoxicology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
3.0field-weighted citation impact, top 8% 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

25 citing papers in PubMed, 49 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

4 authors at 1 institution in 1 country.

Mondona S McCannDepartment of Neuroscience, Georgetown University Medical Center, Washington D.C., United States; Interdisciplinary Program in Neuroscience, Georgetown University Medical Center, Washington D.C., United States.
Harvey R FernandezDepartment of Neuroscience, Georgetown University Medical Center, Washington D.C., United States.
Sarah A FlowersDepartment of Neuroscience, Georgetown University Medical Center, Washington D.C., United States.
Kathleen A Maguire-ZeissDepartment of Neuroscience, Georgetown University Medical Center, Washington D.C., United States; Interdisciplinary Program in Neuroscience, Georgetown University Medical Center, Washington D.C., United States. Electronic address: km445@georgetown.edu.
Georgetown University · US

Funding

Training in Neural Injury &PlasticityT32NS041218 · NINDS · GEORGETOWN UNIVERSITY · PI MARK P BURNS, Kathleen Anne Maguire-Zeiss · 2001 to 2026
$3.5M
Perineuronal proteolysis and circuit dysfunction in HANDR01NS108810 · NINDS · GEORGETOWN UNIVERSITY · PI CONANT, KATHERINE E, MAGUIRE-ZEISS, KATHLEEN ANNE · 2018 to 2022
$1.9M
NINDS NIH HHS R01 NS108810NINDS NIH HHS T32 NS041218
6 · The paper itself

Abstract

Exposure to environmental toxicants is prevalent, hazardous and linked to varied detrimental health outcomes and disease. Polychlorinated biphenyls (PCBs), a class of hazardous organic chlorines once widely used for industrial purposes, are associated with neurodegenerative disease and oxidative stress in both in vitro and in vivo models. Here, we investigated the impact of Aroclor 1254, a commercially available PCB mixture, on primary murine astrocytes to determine the response to this once ubiquitously used toxicant on the most numerous cells of the central nervous system (CNS). Astrocytes are a critical component of homeostasis throughout the CNS, including at the blood-brain barrier, where they serve as the primary defense against xenobiotics entering the CNS, and at the synapse, where they are closely coupled to neurons through several metabolic pathways. We hypothesized that PCBs cause astrocytic oxidative stress and related dysfunction including altered metabolism. We exposed primary murine cortical astrocytes to PCBs and report an increased expression of antioxidant genes (Prdx1, Gsta2, Gfap, Amigo2) in response to oxidative stress. Our data show increased ATP production and spare respiratory capacity in astrocytes exposed to 10 μM (∼ 3 ppm) PCBs. This dose also causes an increase in glucose uptake that is not seen at a higher dose (50 μM) suggesting that, at a lower dose, astrocytes are able to engage compensatory mechanisms to promote survival. Together, these data suggest that exposure to PCBs impact astrocytic metabolism, which is important to consider both in the context of human health and disease and in in vitro and in vivo disease models.

Indexed as

AnimalsAstrocytesBrainCells, CulturedCell SurvivalEnvironmental PollutantsFemaleMaleMiceMice, Inbred C57BLOxidative StressPolychlorinated BiphenylsEnvironmental PollutantsPolychlorinated BiphenylsAntioxidantBrainEnvironmental toxicantGliaglutathioneHomeostasisMitochondriaNeurodegenerationorganochlorineParkinson’s diseaseReactive oxygen speciesSeahorse

Identifiers

PMID34265337
PMCPMC8440398
OpenAlexW3182958880

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.