Evidence map›Paper›PMID 20231449›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2010

Identification of hepatoprotective flavonolignans from silymarin.

Stephen J Polyak, Chihiro Morishima, Volker Lohmann, Sampa Pal, David Y W Lee, Yanze Liu, Tyler N Graf, Nicholas H Oberlies

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 115 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
115citing papers in PubMed, 1 pooled it
30.1field-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

115 citing papers in PubMed, 1 synthesis or guideline pooled it, 309 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
  4. Trial
  5. Trial
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Carbon Monoxide-Releasing Activity of Plant Flavonoids.Journal of agricultural and food chemistry · 2025
    Article
  14. Exploring the chemotypic variability ofFrontiers in plant science · 2025
    Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Chemical Standardization of Milk Thistle (Journal of the American Society for Mass Spectrometry · 2024
    Article
  20. Article

55 more citing papers are in PubMed but not listed here.

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

8 authors at 4 institutions in 3 countries.

Stephen J PolyakDepartment of Laboratory Medicine, Microbiology and Global Health, University of Washington, Seattle, WA 98104, USA. polyak@u.washington.edu
Chihiro Morishima
Volker Lohmann
Sampa Pal
David Y W Lee
Yanze Liu
Tyler N Graf
Nicholas H Oberlies
Directorate of Medicinal and Aromatic Plants Research · INMcLean Hospital · USUniversity of North Carolina at Greensboro · USHeidelberg University · DE

Funding

Mechanisms of Action of Silymarin for Hepatitis CR21AT002895 · NCCIH · UNIVERSITY OF WASHINGTON · PI POLYAK, STEPHEN J. · 2008 to 2009
$444k
NCCIH NIH HHS AT002895NCCIH NIH HHS R21 AT002895
6 · The paper itself

Abstract

Silymarin, also known as milk thistle extract, inhibits hepatitis C virus (HCV) infection and also displays antioxidant, anti-inflammatory, and immunomodulatory actions that contribute to its hepatoprotective effects. In the current study, we evaluated the hepatoprotective actions of the seven major flavonolignans and one flavonoid that comprise silymarin. Activities tested included inhibition of: HCV cell culture infection, NS5B polymerase activity, TNF-alpha-induced NF-kappaB transcription, virus-induced oxidative stress, and T-cell proliferation. All compounds were well tolerated by Huh7 human hepatoma cells up to 80 muM, except for isosilybin B, which was toxic to cells above 10 muM. Select compounds had stronger hepatoprotective functions than silymarin in all assays tested except in T cell proliferation. Pure compounds inhibited JFH-1 NS5B polymerase but only at concentrations above 300 muM. Silymarin suppressed TNF-alpha activation of NF-kappaB dependent transcription, which involved partial inhibition of IkappaB and RelA/p65 serine phosphorylation, and p50 and p65 nuclear translocation, without affecting binding of p50 and p65 to DNA. All compounds blocked JFH-1 virus-induced oxidative stress, including compounds that lacked antiviral activity. The most potent compounds across multiple assays were taxifolin, isosilybin A, silybin A, silybin B, and silibinin, a mixture of silybin A and silybin B. The data suggest that silymarin- and silymarin-derived compounds may influence HCV disease course in some patients. Studies where standardized silymarin is dosed to identify specific clinical endpoints are urgently needed.

Indexed as

Anti-Inflammatory AgentsAntioxidantsAntiviral AgentsCell Line, TumorDrug Evaluation, PreclinicalFlavonolignansHepatitis CHumansImmunologic FactorsLiverNF-kappa BOxidative StressProtective AgentsSilymarinT-LymphocytesAnti-Inflammatory AgentsAntioxidantsAntiviral AgentsFlavonolignansImmunologic FactorsNF-kappa BProtective AgentsSilymarin

Identifiers

PMID20231449
PMCPMC2851903
OpenAlexW2157335302

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.