Evidence map›Paper›PMID 25952541›Full record

ArticleMolecular neurobiology2016

Tea Polyphenols Protect Against Methylmercury-Induced Cell Injury in Rat Primary Cultured Astrocytes, Involvement of Oxidative Stress and Glutamate Uptake/Metabolism Disorders.

Wei Liu, Zhaofa Xu, Tianyao Yang, Yu Deng, Bin Xu, Shu Feng

Abstract read
PubMed Publisher
In one paragraph

Article in Molecular neurobiology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

14 citing papers in PubMed, 24 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

6 authors at 1 institution in 1 country.

Wei LiuDepartment of Environmental Health, School of Public Health, China Medical University, Shenyang, 110122, Liaoning province, China.
Zhaofa XuDepartment of Environmental Health, School of Public Health, China Medical University, Shenyang, 110122, Liaoning province, China. zfxu@mail.cmu.edu.cn.
Tianyao YangDepartment of Environmental Health, School of Public Health, China Medical University, Shenyang, 110122, Liaoning province, China.
Yu DengDepartment of Environmental Health, School of Public Health, China Medical University, Shenyang, 110122, Liaoning province, China.
Bin XuDepartment of Environmental Health, School of Public Health, China Medical University, Shenyang, 110122, Liaoning province, China.
Shu FengDepartment of Environmental Health, School of Public Health, China Medical University, Shenyang, 110122, Liaoning province, China.
China Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Methylmercury (MeHg) is an extremely dangerous environmental contaminant, accumulating preferentially in CNS and causing a series of cytotoxic effects. However, the precise mechanisms are still incompletely understood. The current study explored the mechanisms that contribute to MeHg-induced cell injury focusing on the oxidative stress and Glu uptake/metabolism disorders in rat primary cultured astrocytes. Moreover, the neuroprotective effects of tea polyphenols (TP), a natural antioxidant, against MeHg cytotoxicity were also investigated. Astrocytes were exposed to 0, 2.5, 5, 10, and 20 μM MeHgCl for 6-30 h, or pretreated with 50, 100, 200, and 400 μM TP for 1-12 h; cell viability and LDH release were then determined. For further experiments, 50, 100, and 200 μM of TP pretreatment for 6 h followed by 10 μM MeHgCl for 24 h were performed for the examination of the responses of astrocytes, specifically addressing NPSH levels, ROS generation, ATPase activity, the expressions of Nrf2 pathway as well as Glu metabolism enzyme GS and Glu transporters (GLAST and GLT-1). Exposure of MeHg resulted in damages of astrocytes, which were shown by a loss of cell viability, and supported by high levels of LDH release, morphological changes, apoptosis rates, and NPSH depletion. In addition, astrocytes were sensitive to MeHg-mediated oxidative stress, a finding that is consistent with ROS overproduction; Nrf2 as well as its downstream genes HO-1 and γ-GCSh were markedly upregulated. Moreover, MeHg significantly inhibited GS activity, as well as expressions of GS, GLAST, and GLT-1. On the contrary, pretreatment with TP presented a concentration-dependent prevention against MeHg-mediated cytotoxic effects of astrocytes. In conclusion, the findings clearly indicated that MeHg aggravated oxidative stress and Glu uptake/metabolism dysfunction in astrocytes. TP possesses some abilities to prevent MeHg cytotoxicity through its antioxidative properties.

Indexed as

AstrocytesGlutamic AcidOxidative StressPolyphenolsTeaAnimalsApoptosisCells, CulturedCell ShapeCell SurvivalExcitatory Amino Acid Transporter 1Excitatory Amino Acid Transporter 2Glutamate-Cysteine LigaseHeme Oxygenase-1L-Lactate DehydrogenaseMethylmercury CompoundsExcitatory Amino Acid Transporter 1Excitatory Amino Acid Transporter 2Glutamate-Cysteine LigaseGlutamic AcidHeme Oxygenase-1L-Lactate DehydrogenaseMethylmercury CompoundsNF-E2-Related Factor 2PolyphenolsReactive Oxygen SpeciesSlc1a2 protein, ratSlc1a3 protein, ratSodium-Potassium-Exchanging ATPaseTeaAstrocytesGlutamate metabolismGlutamate uptakeMethylmercuryOxidative stressTea polyphenols

Identifiers

PMID25952541
OpenAlexW2187012574

What OpenQuestion holds

Textmetadata
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.