Evidence map›Paper›PMID 29717768›Full record

ArticleInternational journal of molecular medicine2018

Breviscapine ameliorates CCl4‑induced liver injury in mice through inhibiting inflammatory apoptotic response and ROS generation.

Yu Liu, Pei-Hao Wen, Xin-Xue Zhang, Yang Dai, Qiang He

Open access · hybridAbstract read
In one paragraph

Article in International journal of molecular medicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
8.9field-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

52 citing papers in PubMed, 101 citations in OpenAlex.

  1. Targeted delivery of berberineNanoscale advances · 2026
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  5. Anti-Tumour Immunity Relies on Targeting Tissue Homeostasis Through Monocyte-Driven Responses Rather Than Direct Tumour Cytotoxicity.Liver international : official journal of the International Association for the Study of the Liver · 2025
    Article
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  9. Review
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  11. Review
  12. Article
  13. Review
  14. Article
  15. Article
  16. Oxidative stress in Wernicke's encephalopathy.Frontiers in aging neuroscience · 2023
    Review
  17. Article
  18. Chinese herbal medicines · 2023
    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 1 country.

Yu LiuDepartment of Hepatobiliary Surgery, Beijing Chao‑Yang Hospital Affiliated to Capital University of Medical Science, Beijing 100000, P.R. China.
Pei-Hao WenDepartment of Hepatobiliary Surgery, Beijing Chao‑Yang Hospital Affiliated to Capital University of Medical Science, Beijing 100000, P.R. China.
Xin-Xue ZhangDepartment of Hepatobiliary Surgery, Beijing Chao‑Yang Hospital Affiliated to Capital University of Medical Science, Beijing 100000, P.R. China.
Yang DaiDepartment of Hepatobiliary Surgery, Beijing Chao‑Yang Hospital Affiliated to Capital University of Medical Science, Beijing 100000, P.R. China.
Qiang HeDepartment of Hepatobiliary Surgery, Beijing Chao‑Yang Hospital Affiliated to Capital University of Medical Science, Beijing 100000, P.R. China.
Beijing Chao-Yang Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Acute liver injury is characterized by fibrosis, inflammation and apoptosis, leading to liver failure, cirrhosis or cancer and affecting the clinical outcome in the long term. However, no effective therapeutic strategy is currently available. Breviscapine, a mixture of flavonoid glycosides, has been reported to have multiple biological functions. The present study aimed to investigate the effects of breviscapine on acute liver injury induced by CCl4 in mice. C57BL/6 mice were subjected to intraperitoneal injection with CCl4 for 8 weeks with or without breviscapine (15 or 30 mg/kg). Mice treated with CCl4 developed acute liver injury, as evidenced by histological analysis, Masson trichrome and Sirius Red staining, accompanied with elevated levels of alanine aminotransferase and aspartate aminotransferase. Furthermore, increases in pro‑inflammatory cytokines, chemokines and apoptotic factors, including caspase‑3 and poly(ADP ribose) polymerase‑2 (PARP‑2), were observed. Breviscapine treatment significantly and dose‑dependently reduced collagen deposition and the fibrotic area. Inflammatory cytokines were downregulated by breviscapine through inactivating Toll‑like receptor 4/nuclear factor-κB signaling pathways. In addition, co‑administration of breviscapine with CCl4 decreased the apoptotic response by enhancing B‑cell lymphoma-2 (Bcl‑2) levels, while reducing Bcl‑2‑associated X protein, apoptotic protease activating factor 1, caspase‑3 and PARP activity. Furthermore, CCl4‑induced oxidative stress was blocked by breviscapine through improving anti‑oxidants and impeding mitogen‑activated protein kinase pathways. The present study highlighted that breviscapine exhibited liver‑protective effects against acute hepatic injury induced by CCl4 via suppressing inflammation and apoptosis.

Indexed as

Carbon TetrachlorideAnimalsAnti-Inflammatory AgentsAntioxidantsApoptosisCell LineChemical and Drug Induced Liver InjuryCytokinesFlavonoidsHumansInflammationLiverMaleMice, Inbred C57BLRatsReactive Oxygen SpeciesAnti-Inflammatory AgentsAntioxidantsbreviscapineCarbon TetrachlorideCytokinesFlavonoidsReactive Oxygen Species

Identifiers

PMID29717768
PMCPMC6034936
OpenAlexW2799726777

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.