Evidence map›Paper›PMID 25361427›Full record

ArticleMolecules (Basel, Switzerland)2014

β-sitosterol protects against carbon tetrachloride hepatotoxicity but not gentamicin nephrotoxicity in rats via the induction of mitochondrial glutathione redox cycling.

Hoi-Shan Wong, Ji-Hang Chen, Pou-Kuan Leong, Hoi-Yan Leung, Wing-Man Chan, Kam-Ming Ko

Abstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing 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

18 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Sesame Seeds: A Nutrient-Rich Superfood.Foods (Basel, Switzerland) · 2024
    Review
  5. Article
  6. Review
  7. BioMed research international · 2021
    Article
  8. Article
  9. Article
  10. Article
  11. Evidence-based complementary and alternative medicine : eCAM · 2020
    Article
  12. Article
  13. Article
  14. Flavonoids, Sterols and Lignans fromMolecules (Basel, Switzerland) · 2018
    Article
  15. Analysis of antioxidative and antiviral biomarkers β-amyrin, β-sitosterol, lupeol, ursolic acid inSaudi pharmaceutical journal : SPJ : the official publication of the Saudi Pharmaceutical Society · 2018
    Article
  16. Article
  17. Article
  18. 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

6 authors.

Hoi-Shan WongDivision of Life Science, Hong Kong University of Science and Technology, Hong Kong, China. bchelenwong@ust.hk.
Ji-Hang ChenDivision of Life Science, Hong Kong University of Science and Technology, Hong Kong, China. cjh@ust.hk.
Pou-Kuan LeongDivision of Life Science, Hong Kong University of Science and Technology, Hong Kong, China. eriol@ust.hk.
Hoi-Yan LeungDivision of Life Science, Hong Kong University of Science and Technology, Hong Kong, China. hoiyan@ust.hk.
Wing-Man ChanDivision of Life Science, Hong Kong University of Science and Technology, Hong Kong, China. wingman@ust.hk.
Kam-Ming KoDivision of Life Science, Hong Kong University of Science and Technology, Hong Kong, China. bcrko@ust.hk.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Previous findings have demonstrated that β-sitosterol (BSS), an active component of Cistanches Herba, protected against oxidant injury in H9c2 cardiomyocytes and in rat hearts by enhancing mitochondrial glutathione redox cycling, possibly through the intermediacy of mitochondrial reactive oxygen species production. We therefore hypothesized that BSS pretreatment can also confer tissue protection against oxidant injury in other vital organs such as liver and kidney of rats. In this study, the effects of BSS pretreatment on rat models of carbon tetrachloride (CCl4) hepatotoxicity and gentamicin nephrotoxicity were investigated. The findings showed that BSS pretreatment protected against CCl4-induced hepatotoxicity, but not gentamicin nephrotoxicity in rats. The hepatoprotection afforded by BSS was associated with the improvement in mitochondrial glutathione redox status, presumably through the glutathione reductase-mediated enhancement in mitochondrial glutathione redox cycling. The hepatoprotection afforded by BSS was also accompanied by the improved mitochondrial functional ability in rat livers. The inability of BSS to protect against gentamicin nephrotoxicity was likely due to the relatively low bioavailability of BSS in rat kidneys. BSS may serve as potential mitohormetic agent for the prevention of oxidative stress-induced injury in livers.

Indexed as

AnimalsAntioxidantsBiological AvailabilityCarbon TetrachlorideChemical and Drug Induced Liver InjuryFemaleGentamicinsGlutathioneGlutathione ReductaseKidneyKidney DiseasesLiverMitochondriaOxidantsOxidation-ReductionOxidative StressAntioxidantsCarbon Tetrachloridegamma-sitosterolGentamicinsGlutathioneGlutathione ReductaseOxidantsReactive Oxygen SpeciesSitosterols

Identifiers

PMID25361427
PMCPMC6271253

What OpenQuestion holds

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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.