Evidence map›Paper›PMID 27043523›Full record

ArticleMolecules (Basel, Switzerland)2016

Silymarin Prevents Restraint Stress-Induced Acute Liver Injury by Ameliorating Oxidative Stress and Reducing Inflammatory Response.

Sou Hyun Kim, Dal-Seok Oh, Ji Youn Oh, Tae Gen Son, Dong Yeon Yuk, Young-Suk Jung

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
5.4field-weighted citation impact, top 4% 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

26 citing papers in PubMed, 64 citations in OpenAlex.

  1. Article
  2. Review
  3. Milk Thistle (Current medicinal chemistry · 2025
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  7. Article
  8. Silymarin and Inflammation: Food for Thoughts.Antioxidants (Basel, Switzerland) · 2024
    Review
  9. Article
  10. Article
  11. Review
  12. Shibi Tea (Nutrients · 2022
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. An Herbal Formula CGFrontiers in pharmacology · 2020
    Article
  19. Article
  20. 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

6 authors at 4 institutions in 1 country.

Sou Hyun KimCollege of Pharmacy, Pusan National University, Busan 609-735, Korea. hyunie9808@naver.com.
Dal-Seok OhThe K-herb Research Center, Korea Institute of Oriental Medicine, Daejeon 305-811, Korea. dalsoh@gmail.com.
Ji Youn OhCollege of Pharmacy, Pusan National University, Busan 609-735, Korea. pooh7282@naver.com.
Tae Gen SonDivision for Research Center, Dongnam Institute of Radiological and Medical Science, Busan 619-953, Korea. tgson@hanmail.net.
Dong Yeon YukCollege of Pharmacy, Chungbuk National University, Cheongju 361-763, Korea. julycosmos@gmail.com.
Young-Suk JungCollege of Pharmacy, Pusan National University, Busan 609-735, Korea. youngjung@pusan.ac.kr.
Pusan National University · KRChungbuk National University · KRDongnam Institute of Radiological & Medical Sciences · KRKorea Institute of Oriental Medicine · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Silymarin is a flavonoid extracted from the milk thistle Silybum marianum. It has been reported to prevent liver injuries induced by various chemicals or toxins. Our recent study suggested that silymarin induces hepatic synthesis of glutathione by increasing cysteine availability, which may consequently contribute to increased antioxidant capacity of the liver. In the present study, we investigated the effects of silymarin on acute liver injury induced by restraint stress. Silymarin (100 mg/kg) was orally administered to BALB/c mice every 12 h (3 times in total). After the last dose, mice were subjected to restraint stress for 6 h, and serum levels of aspartate and alanine aminotransferases, and hepatic levels of lipid peroxidation were determined. Hepatic levels of sulfur-containing metabolites such as methionine, S-adenosylmethionine, cysteine, and glutathione were also measured. The level of pro-inflammatory mediators in both liver and serum was determined. To study the mechanism of the effects of silymarin, we assessed Jun N-terminal kinase (JNK) activation and apoptotic signaling. Restraint stress induced severe oxidative stress and increased mRNA levels of pro-inflammatory mediators; both effects of restraint stress were significantly inhibited by silymarin. Moreover, administration of silymarin significantly prevented acute liver injury induced by restraint stress by blocking JNK activation and subsequently apoptotic signaling. In conclusion, these results suggest that the inhibition of restraint stress-induced liver injury by silymarin is due at least in part to its anti-oxidant activity and its ability to suppress the inflammatory response.

Indexed as

Acute Lung InjuryAnimalsAntioxidantsApoptosisHumansInflammationLipid PeroxidationLiverMiceOxidative StressSilybum marianumSilymarinAntioxidantsSilymarinacute liver injuryinflammationoxidative stressrestraint stresssilymarin

Identifiers

PMID27043523
PMCPMC6274117
OpenAlexW2325863196

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.