Evidence map›Paper›PMID 33537886›Full record

ArticleArchives of pharmacal research2021

Protective effects of ginsenoside-Rg2 and -Rh1 on liver function through inhibiting TAK1 and STAT3-mediated inflammatory activity and Nrf2/ARE-mediated antioxidant signaling pathway.

Thuy Le Lam Nguyen, Diem Thi Ngoc Huynh, Yujin Jin, Hyesu Jeon, Kyung-Sun Heo

Abstract read
PubMed Publisher
In one paragraph

Article in Archives of pharmacal research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
3.0field-weighted citation impact, top 8% 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

27 citing papers in PubMed, 45 citations in OpenAlex.

  1. Ginsenoside Rg2 fromMolecules (Basel, Switzerland) · 2026
    Review
  2. Article
  3. Article
  4. Protective effect of 6'-Sialyllactose on LPS-induced macrophage inflammationThe Korean journal of physiology & pharmacology : official journal of the Korean Physiological Society and the Korean Society of Pharmacology · 2024
    Article
  5. Article
  6. Article
  7. Review
  8. Experimental model and novel therapeutic targets for non-alcoholic fatty liver disease development.The Korean journal of physiology & pharmacology : official journal of the Korean Physiological Society and the Korean Society of Pharmacology · 2023
    Review
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Roles of ginsenosides in sepsis.Journal of ginseng research · 2023
    Review
  16. Effects ofFrontiers in veterinary science · 2023
    Article
  17. Article
  18. Article
  19. Article
  20. 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 1 institution in 2 countries.

Thuy Le Lam Nguyen *College of Pharmacy and Institute of Drug Research and Development, Chungnam National University, Daejeon, South Korea.
Diem Thi Ngoc Huynh *College of Pharmacy and Institute of Drug Research and Development, Chungnam National University, Daejeon, South Korea.
Yujin JinCollege of Pharmacy and Institute of Drug Research and Development, Chungnam National University, Daejeon, South Korea.
Hyesu JeonCollege of Pharmacy and Institute of Drug Research and Development, Chungnam National University, Daejeon, South Korea.
Kyung-Sun HeoCollege of Pharmacy and Institute of Drug Research and Development, Chungnam National University, Daejeon, South Korea. kheo@cnu.ac.kr.ORCID http://orcid.org/0000-0003-3800-7665
Chungnam National University · KR

Funding

National Research Foundation of Korea 2019R1C1C100733112
6 · The paper itself

Abstract

Systemic or hepatic inflammation is caused by intraperitoneal application of lipopolysaccharide (LPS). In this study, we investigated anti-inflammatory and antioxidant properties of combination of ginsenoside-Rg2 (G-Rg2) and -Rh1 (G-Rh1) on liver function under LPS challenging. We first confirmed that G-Rg2 and -Rh1 at 100 μg/ml did not show cytotoxicity in HepG2 cells. G-Rg2 and -Rh1 treatment significantly inhibited activation of STAT3 and TAK1, and inflammatory factors including iNOS, TNF-α, and IL-1β in peritoneal macrophages. In HepG2 cells, G-Rg2 and -Rh1 treatment inhibited activation of STAT3 and TAK1/c-Jun N-terminal kinase, and down-regulated nuclear translocation of NF-κB transcription factor. In addition, LPS-induced mitochondrial dysfunction was restored by treatment with G-Rg2 and -Rh1. Interestingly, pretreatment with G-Rg2 and -Rh1 effectively inhibited mitochondrial damage-mediated ROS production induced by LPS stimulation, and alterations of Nrf2 nuclear translocation and ARE promotor activity were involved in G-Rg2 and -Rh1 effects on balancing ROS levels. In liver tissues of LPS-treated mice, G-Rg2 and -Rh1 treatment protected liver damages and increased Nrf2 expression while reducing CD45 expression. Taken together, G-Rg2 and -Rh1 exerts a protective effect on liver function by increasing antioxidant through Nrf2 and anti-inflammatory activities through STAT3/TAK1 and NF-κB signaling pathways in liver cells and macrophages.

Indexed as

AnimalsAnti-Inflammatory AgentsAntioxidantsDose-Response Relationship, DrugGinsenosidesHep G2 CellsHumansLiverMaleMAP Kinase Kinase Kinase 7MAP Kinase Kinase KinasesMiceMice, Inbred ICRNF-E2-Related Factor 2Signal TransductionSTAT3 Transcription FactorAnti-Inflammatory AgentsAntioxidantsginsenoside Rg2ginsenoside Rh1GinsenosidesMAP Kinase Kinase Kinase 7MAP Kinase Kinase KinasesNfe2l2 protein, mouseNF-E2-Related Factor 2Stat3 protein, mouseSTAT3 Transcription FactorAnti-inflammatoryAntioxidantGinsenoside-Rg2 and Rh1Liver functionNrf2STAT3/TAK1

Identifiers

PMID33537886
OpenAlexW3127821983

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.