Evidence map›Paper›PMID 35024184›Full record

ArticleJournal of advanced research2021

Hyperoside attenuates non-alcoholic fatty liver disease in rats via cholesterol metabolism and bile acid metabolism.

Songsong Wang, Feiya Sheng, Liang Zou, Jianbo Xiao, Peng Li

Open access · goldAbstract read
In one paragraph

Article in Journal of advanced research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 68 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
68citing papers in PubMed, 1 pooled it
13.1field-weighted citation impact, top 1% 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

68 citing papers in PubMed, 1 synthesis or guideline pooled it, 163 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
  4. Article
  5. Total Flavonoids ofNutrients · 2026
    Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Review

8 more citing papers are in PubMed but not listed here.

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 3 institutions in 3 countries.

Songsong WangState Key Laboratory of Quality Research in Chinese Medicine, Institute of Chinese Medical Sciences, University of Macau, Macao 999078, China.
Feiya ShengState Key Laboratory of Quality Research in Chinese Medicine, Institute of Chinese Medical Sciences, University of Macau, Macao 999078, China.
Liang ZouSchool of Medicine, Chengdu University, Chengdu 610106, China.
Jianbo XiaoInstitute of Food Safety and Nutrition, Jinan University, Guangzhou 510632, China.
Peng LiState Key Laboratory of Quality Research in Chinese Medicine, Institute of Chinese Medical Sciences, University of Macau, Macao 999078, China.
University of Macau · MOChengdu University · CNJinan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Non-alcoholic fatty liver disease (NAFLD) results from increased hepatic total cholesterol (TC) and total triglyceride (TG) accumulation. In our previous study, we found that rats treated with hyperoside became resistant to hepatic lipid accumulation. Objectives: The present study aims to investigate the possible mechanisms responsible for the inhibitory effects of hyperoside on the lipid accumulation in the liver tissues of the NAFLD rats. Methods: Label-free proteomics and metabolomics targeting at bile acid (BA) metabolism were applied to disclose the mechanisms for hyperoside reducing hepatic lipid accumulation among the NAFLD rats. Results: In response to hyperoside treatment, several proteins related to the fatty acid degradation pathway, cholesterol metabolism pathway, and bile secretion pathway were altered, including ECI1, Acnat2, ApoE, and BSEP, etc. The expression of nuclear receptors (NRs), including farnesoid X receptor (FXR) and liver X receptor α (LXRα), were increased in hyperoside-treated rats' liver tissue, accompanied by decreased protein expression of catalyzing enzymes in the hepatic Conclusions: Taken together, the results suggest that hyperoside could improve the condition of NAFLD by regulating the cholesterol metabolism as well as BAs metabolism and excretion. These findings contribute to understanding the mechanisms by which hyperoside lowers the cholesterol and triglyceride in NAFLD rats.

Indexed as

Non-alcoholic Fatty Liver DiseaseAnimalsBile Acids and SaltsCholesterolLipid MetabolismQuercetinRatsBile Acids and SaltsCholesterolhyperosideQuercetinACC, Acetyl-CoA carboxylaseAMPK, AMP-activated protein kinaseApo, apolipoproteinBAs, bile acidsBile acid metabolismBSH, bile salt hydrolaseCholesterol metabolismCYP27A1, sterol 27-hydroxylaseCYP7A1, cholesterol 7α-hydroxylaseFGF15/19, fibroblast growth factor 15/19FXR, farnesoid X receptorHyperosideLabel-free proteomicsLC-MS, the combination of high-performance liquid chromatography and mass spectrometryLXRα, liver X receptor αNAFLDNAFLD, non-alcoholic fatty liver diseasepACC, phosphorylated ACCPMSF, phenylmethylsulfonyl fluorideQC, quality controlSDS, sodium dodecyl sulfateSHP, small heterodimer partnerSREBP1, sterol regulatory element-binding protein 1SREBP2, sterol regulatory element-binding protein 2SREBPs, sterol regulatory element binding proteinsTargeted metabolomicsTC, total cholesterolTGR5, Takeda G-protein-coupled receptor 5TG, triglycerideVLDL, very low-density lipoproteinWB, Western blot

Identifiers

PMID35024184
PMCPMC8655136
OpenAlexW3172197894

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.