Evidence map›Paper›PMID 24690763›Full record

ArticlePloS one2014

Hepatoprotective bioactivity of the glycoprotein, antrodan, isolated from Antrodia cinnamomea mycelia.

Yaw-Bee Ker, Chiung-Chi Peng, Wan-Lin Chang, Charng-Cherng Chyau, Robert Y Peng

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 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.9field-weighted citation impact, top 11% 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

16 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
  2. Comparative Efficacy ofAntioxidants (Basel, Switzerland) · 2025
    Article
  3. Review
  4. Review
  5. Safety of freeze-dried mycelia ofEFSA journal. European Food Safety Authority · 2022
    Article
  6. Article
  7. Article
  8. Effect of ethanol extracts of Antrodia cinnamomea on head and neck squamous cell carcinoma cell line.Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica · 2020
    Article
  9. Article
  10. Article
  11. Amelioration of carbon tetrachloride-induced hepatic injury by emulsifiedIranian journal of basic medical sciences · 2018
    Article
  12. International journal of biological sciences · 2018
    Article
  13. Article
  14. Article
  15. Article
  16. 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

5 authors at 2 institutions in 1 country.

Yaw-Bee KerDepartment of Applied Food Technology, Hungkuang University, Taichung, Taiwan, ROC.
Chiung-Chi PengGraduate Institute of Clinical Medicine, College of Medicine, Taipei Medical University, Taipei, Taiwan, ROC.
Wan-Lin ChangResearch Institute of Biotechnology, Hungkuang University, Taichung, Taiwan, ROC.
Charng-Cherng ChyauResearch Institute of Biotechnology, Hungkuang University, Taichung, Taiwan, ROC.
Robert Y PengResearch Institute of Biotechnology, Hungkuang University, Taichung, Taiwan, ROC.
Hungkuang University · TWTaipei Medical University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Antrodan, a protein-bound polysaccharide isolated from Antrodia cinnamomea mycelia, was demonstrated to exhibit significant anti-inflammatory bioactivity in vitro. However, its role in hepatic injury in vivo still remains unclear. We hypothesized that antrodan may have beneficial hepatoprotective effects. To verify this, a lipopolysaccharide (LPS)-Sprague-Dawley rat model was used. Antrodan protected against liver damage by suppressing LPS-stimulated serum glutamine-oxaloacetic transaminase (GOT), glutamic-pyruvic transaminase (GPT), interleukin (IL)-6, hepatic thiobarbituric acid reactive substances (TBARS), nitric oxide (NO), inducible NO synthase (iNOS) and nuclear factor (NF)-κB, and by effectively alleviating the downregulated hepatic superoxide dismutase (SOD), catalase, and glutathione peroxidase (GSH-Px). Hematoxylin-eosin staining revealed that antrodan at a dosage of 40 mg/kg was able to alleviate LPS-induced liver damage to a normal status. In addition, we identified the partial main architectural backbone of antrodan to have a 1 → 3 linear β-glycosidic backbone of mannan linked by β-1 → 3 glucosidic branches. Conclusively, antrodan can potentially ameliorate liver damage in vivo by suppressing oxidative stress induced by LPS.

Indexed as

MyceliumAnimalsAntioxidantsAntrodiaFungal ProteinsGlycoproteinsInterleukin-6LiverLiver Function TestsMaleNF-kappa BNitric OxideNitric Oxide Synthase Type IIOxidation-ReductionProtective AgentsRatsAntioxidantsFungal ProteinsGlycoproteinsInterleukin-6NF-kappa BNitric OxideNitric Oxide Synthase Type IIProtective AgentsThiobarbituric Acid Reactive Substances

Identifiers

PMID24690763
PMCPMC3972158
OpenAlexW2037850871

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.