Evidence map›Paper›PMID 24988078›Full record

ArticlePloS one2014

Activation of Nrf2 protects against triptolide-induced hepatotoxicity.

Jia Li, Feihai Shen, Cuiwen Guan, Wenwen Wang, Xiaozhe Sun, Xinlu Fu, Min Huang, Jing Jin, Zhiying Huang

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
22.8field-weighted citation impact, top 1% 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

47 citing papers in PubMed, 102 citations in OpenAlex.

  1. Article
  2. CD4Frontiers in immunology · 2026
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  10. Review
  11. The Nrf2 Pathway in Liver Diseases.Frontiers in cell and developmental biology · 2022
    Review
  12. Review
  13. Review
  14. Article
  15. Review
  16. Frontiers in pharmacology · 2021
    Review
  17. Article
  18. Article
  19. Article
  20. A review of the total syntheses of triptolide.Beilstein journal of organic chemistry · 2019
    Review
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

9 authors at 1 institution in 1 country.

Jia LiSchool of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou, China; Pharmaceutical Department, Affiliated Cancer Hospital of Guangzhou Medical University, Guangzhou, China.
Feihai ShenSchool of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou, China.
Cuiwen GuanSchool of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou, China.
Wenwen WangSchool of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou, China.
Xiaozhe SunSchool of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou, China.
Xinlu FuCenter of Laboratory Animals, Sun Yat-sen University, Guangzhou, China.
Min HuangSchool of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou, China.
Jing JinSchool of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou, China.
Zhiying HuangSchool of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou, China; Center of Laboratory Animals, Sun Yat-sen University, Guangzhou, China.
Sun Yat-sen University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Triptolide, the major active component of Tripterygium wilfordii Hook f. (TWHF), has a wide range of pharmacological activities. However, the toxicities of triptolide, particularly the hepatotoxicity, limit its clinical application. The hepatotoxicity of triptolide has not been well characterized yet. The aim of this study was to investigate the role of NF-E2-related factor 2 (Nrf2) in triptolide-induced toxicity and whether activation of Nrf2 could protect against triptolide-induced hepatotoxicity. The results showed that triptolide caused oxidative stress and cell damage in HepG2 cells, and these toxic effects could be aggravated by Nrf2 knockdown or be counteracted by overexpression of Nrf2. Treatment with a typical Nrf2 agonist, sulforaphane (SFN), attenuated triptolide-induced liver dysfunction, structural damage, glutathione depletion and decrease in antioxidant enzymes in BALB/C mice. Moreover, the hepatoprotective effect of SFN on triptolide-induced liver injury was associated with the activation of Nrf2 and its downstream targets. Collectively, these results indicate that Nrf2 activation protects against triptolide-induced hepatotoxicity.

Indexed as

AnimalsAnticarcinogenic AgentsAntineoplastic Agents, AlkylatingChemical and Drug Induced Liver InjuryDiterpenesEpoxy CompoundsHep G2 CellsHumansIsothiocyanatesMiceMice, Inbred BALB CNF-E2-Related Factor 2Oxidative StressPhenanthrenesSulfoxidesAnticarcinogenic AgentsAntineoplastic Agents, AlkylatingDiterpenesEpoxy CompoundsIsothiocyanatesNFE2L2 protein, humanNfe2l2 protein, mouseNF-E2-Related Factor 2PhenanthrenessulforaphaneSulfoxidestriptolide

Identifiers

PMID24988078
PMCPMC4079517
OpenAlexW1983779246

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.