Evidence map›Paper›PMID 25143196›Full record

ArticlePharmaceutical research2015

Protective effects of calycosin against CCl4-induced liver injury with activation of FXR and STAT3 in mice.

Xinli Chen, Qiang Meng, Changyuan Wang, Qi Liu, Huijun Sun, Xiaokui Huo, Pengyuan Sun, Xiaobo Yang, Jinyong Peng, Kexin Liu

Abstract read
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In one paragraph

Article in Pharmaceutical research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.2field-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

19 citing papers in PubMed, 48 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Review
  6. Farnesoid X receptor regulators from natural products and their biological function.Journal of traditional Chinese medicine = Chung i tsa chih ying wen pan · 2023
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  7. Review
  8. Chemical Composition ofMolecules (Basel, Switzerland) · 2022
    Article
  9. Article
  10. 5-O-Demethylnobiletin Alleviates CClInternational journal of molecular sciences · 2021
    Article
  11. Review
  12. Article
  13. Protective Effect of a Mixture ofEvidence-based complementary and alternative medicine : eCAM · 2020
    Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Down-regulation of ribosomal protein S15A inhibits proliferation of human glioblastoma cells in vivo and in vitro via AKT pathway.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2016
    Article
  19. 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

10 authors at 1 institution in 1 country.

Xinli ChenDepartment of Clinical Pharmacology, College of Pharmacy, Dalian Medical University, 9 West Section, Lvshun South Road, Lvshunkou District, Dalian, Liaoning, 116044, People's Republic of China.
Qiang Meng
Changyuan Wang
Qi Liu
Huijun Sun
Xiaokui Huo
Pengyuan Sun
Xiaobo Yang
Jinyong Peng
Kexin Liu
Dalian Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeInvestigating the hepatoprotective effect of calycosin against acute liver injury in association with FXR activation and STAT3 phosphorylation.

methodsThe acute liver injury model was established by intraperitoneal injection of CCl4 in C57BL/6 mice. Serum alanine aminotransferase, aspartate aminotransferase, HE staining and TUNEL assay were used to identify the amelioration of the liver histopathological changes and hepatocytes apoptosis after calycosin treatment. ELISA kit and 5-bromo-2-deoxyuridine immunohistochemistry were used to measure the liver bile acid concentration and hepatocyte mitotic rate in vivo. The relation between calycosin and activation of FXR and STAT3 was comfirmed using the Luciferase assay, Molecular docking, Real-time PCR and Western Blot in vitro.

resultsThe liver histopathological changes, hepatocytes apoptosis, liver bile acid overload and hepatocyte mitosis showed significant changes after calycosin treatment. Calycosin promoted the expression of FXR target genes such as FoxM1B and SHP but the effect was reversed by FXR suppressor guggulsterone. Molecular docking results indicated that calycosin could be embedded into the binding pocket of FXR, thereby increasing the expressions of STAT3 tyrosine phosphorylation and its target genes, Bcl-xl and SOCS3.

conclusionsCalycosin plays a critical role in hepatoprotection against liver injury in association with FXR activation and STAT3 phosphorylation.

Indexed as

AnimalsCarbon TetrachlorideChemical and Drug Induced Liver InjuryDrugs, Chinese HerbalHep G2 CellsHumansIsoflavonesMaleMiceMice, Inbred C57BLProtective AgentsReceptor, Farnesoid X-ActivatedReceptors, Cytoplasmic and NuclearSTAT3 Transcription Factor7,3'-dihydroxy-4'-methoxyisoflavoneCarbon TetrachlorideDrugs, Chinese HerbalIsoflavonesProtective AgentsReceptor, Farnesoid X-ActivatedReceptors, Cytoplasmic and NuclearStat3 protein, mouseSTAT3 Transcription Factor

Identifiers

PMID25143196
OpenAlexW1975247277

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.