Evidence map›Paper›PMID 27248993›Full record

ArticleMolecules (Basel, Switzerland)2016

Metabolic Profile Changes of CCl₄-Liver Fibrosis and Inhibitory Effects of Jiaqi Ganxian Granule.

Ge Wang, Zehao Li, Hao Li, Lidan Li, Jian Li, Changyuan Yu

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 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.4field-weighted citation impact, top 18% 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

11 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Life (Basel, Switzerland) · 2024
    Article
  3. Review
  4. Article
  5. Article
  6. Antioxidant, anti-inflammatory and anti-fibrotic effects ofExperimental and therapeutic medicine · 2020
    Article
  7. Review
  8. Article
  9. Review
  10. Article
  11. 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

6 authors at 2 institutions in 1 country.

Ge WangCollege of Life Science and Technology, Beijing University of Chemical Technology, Beijing 100029, China. wanggebuct@163.com.
Zehao LiCollege of Life Science and Technology, Beijing University of Chemical Technology, Beijing 100029, China. lizehao1990@126.com.
Hao LiCollege of Life Science and Technology, Beijing University of Chemical Technology, Beijing 100029, China. lihao@buct.edu.cn.
Lidan LiCollege of Life Science and Technology, Beijing University of Chemical Technology, Beijing 100029, China. cd_lilidan@163.com.
Jian LiSchool of Basic Medical Science, Beijing University of Chinese Medicine, Beijing 100029, China. lijiancn922@126.com.
Changyuan YuCollege of Life Science and Technology, Beijing University of Chemical Technology, Beijing 100029, China. yucy@mail.buct.edu.cn.
Beijing University of Chemical Technology · CNBeijing University of Chinese Medicine · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Jiaqi Ganxian Granule (JGG) is a famous traditional Chinese medicine, which has been long used in clinical practice for treating liver fibrosis. However, the mechanism underlying its anti-hepatic fibrosis is still not clear. In this study, an Ultra-Performance Liquid Chromatography-Time-Of-Flight Mass Spectrometry (UPLC-TOF-MS)-based metabolomics strategy was used to profile the metabolic characteristic of serum obtained from a carbon tetrachloride (CCl₄)-induced hepatic fibrosis model in Sprague-Dawley (SD) rats with JGG treatment. Through Principal Component Analysis (PCA) and Partial Least Square Discriminant Analysis (PLS-DA), it was shown that metabolic perturbations induced by CCl₄ were inhibited after treatment of JGG, for 17 different metabolites related to CCl₄. Among these compounds, the change tendency of eight potential drug targets was restored after the intervention with JGG. The current study indicates that JGG has a significant anti-fibrosis effect on CCl₄-induced liver fibrosis in rats, which might be by regulating the dysfunction of sphingolipid metabolism, glycerophospholipid metabolism, N-acylethanolamine biosynthesis, fat digestion and absorption, while glycerophospholipid metabolism played vital roles in the inhibitory effects of JGG on hepatic fibrosis according to Metabolic Pathway Analysis (MetPA). Our findings indicated that the metabolomics approach may provide a useful tool for exploring potential biomarkers involved in hepatic fibrosis and elucidate the mechanisms underlying the action of therapies used in traditional Chinese medicine.

Indexed as

MetabolomeMetabolomicsAnimalsBiomarkersCarbon TetrachlorideChromatography, LiquidDisease Models, AnimalDrugs, Chinese HerbalEnergy MetabolismLiver CirrhosisMaleMedicine, Chinese TraditionalMetabolic Networks and PathwaysRatsSpectrometry, Mass, Matrix-Assisted Laser Desorption-IonizationBiomarkersCarbon TetrachlorideDrugs, Chinese HerbalJiaqi Ganxian granuleliver fibrosismetabolomics pathwayserumultra-performance liquid chromatography-time-of-flight mass spectrometry

Identifiers

PMID27248993
PMCPMC6273034
OpenAlexW2409506259

What OpenQuestion holds

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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.