Evidence map›Paper›PMID 33438347›Full record

ArticleJournal of cellular and molecular medicine2021

PPARγ/NF-κB and TGF-β1/Smad pathway are involved in the anti-fibrotic effects of levo-tetrahydropalmatine on liver fibrosis.

Qiang Yu, Ping Cheng, Jianye Wu, Chuanyong Guo

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
6.7field-weighted citation impact, top 2% 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

28 citing papers in PubMed, 63 citations in OpenAlex.

  1. Review
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  10. A NovelInternational journal of molecular sciences · 2024
    Article
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  13. Article
  14. Article
  15. Article
  16. Towards a Unified Approach in Autoimmune Fibrotic Signalling Pathways.International journal of molecular sciences · 2023
    Review
  17. Insights on drug and gene delivery systems in liver fibrosis.Asian journal of pharmaceutical sciences · 2023
    Review
  18. Review
  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

4 authors at 2 institutions in 1 country.

Qiang YuDepartment of Gastroenterology, Putuo People's Hospital, Tongji University School of Medicine, Shanghai, China.
Ping ChengDepartment of Gerontology, Shanghai Minhang District Central Hospital, Shanghai, China.
Jianye WuDepartment of Gastroenterology, Putuo People's Hospital, Tongji University School of Medicine, Shanghai, China.
Chuanyong GuoDepartment of Gastroenterology, Putuo People's Hospital, Tongji University School of Medicine, Shanghai, China.ORCID 0000-0002-6527-4673
Tongji University · CNMinhang District Central Hospital · CN

Funding

National Natural Science Foundation of China 81670472the Foundation of Minhang Hospital 2018MHJC08the Health System Innovation Project of Shanghai Putuo Science and Technology Commission PTKWWS201801the Health System Innovation Project of Shanghai Putuo Science and Technology Commission PTKWWS201903the Natural Science Foundation of Shanghai 19ZR1447700the Yangfan Project of Shanghai Science and Technology Commission 20YF1443300WBN Hepatology Research Fund of China Hepatitis Prevention and Treatment Foundation CFHPC2019031
6 · The paper itself

Abstract

Liver fibrosis is a necessary stage in the development of chronic liver diseases to liver cirrhosis. This study aims to investigate the anti-fibrotic effects of levo-tetrahydropalmatine (L-THP) on hepatic fibrosis in mice and cell models and its underlying mechanisms. Two mouse hepatic fibrosis models were generated in male C57 mice by intraperitoneal injection of carbon tetrachloride (CCl4) for 2 months and bile duct ligation (BDL) for 14 days. Levo-tetrahydropalmatine was administered orally at doses of 20 and 40 mg/kg. An activated LX2 cell model induced by TGF-β1 was also generated. The results showed that levo-tetrahydropalmatine alleviated liver fibrosis by inhibiting the formation of extracellular matrix (ECM) and regulating the balance between TIMP1 and MMP2 in the two mice liver fibrosis models and cell model. Levo-tetrahydropalmatine inhibited activation and autophagy of hepatic stellate cells (HSCs) by modulating PPARγ/NF-κB and TGF-β1/Smad pathway in vivo and in vitro. In conclusion, levo-tetrahydropalmatine attenuated liver fibrosis by inhibiting ECM deposition and HSCs autophagy via modulation of PPARγ/NF-κB and TGF-β1/Smad pathway.

Indexed as

AnimalsBerberine AlkaloidsBiomarkersCarbon TetrachlorideDisease Models, AnimalExtracellular Matrix ProteinsHepatic Stellate CellsImmunohistochemistryLiver CirrhosisLiver Function TestsMaleMiceNF-kappa BPPAR gammaSignal TransductionSmad ProteinsBerberine AlkaloidsBiomarkersCarbon TetrachlorideExtracellular Matrix ProteinsNF-kappa BPPAR gammaSmad ProteinstetrahydropalmatineTGFB1 protein, humanTransforming Growth Factor beta1autophagylevo-tetrahydropalmatineliver fibrosisPPARγ/NF-κBTGF-β1/Smad

Identifiers

PMID33438347
PMCPMC7875896
OpenAlexW3120352650

What Socratic 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 Socratic graph.