Evidence map›Paper›PMID 24797163›Full record

ArticleScientific reports2014

Lipid modulatory activities of Cichorium glandulosum Boiss et Huet are mediated by multiple components within hepatocytes.

Lin Ding, Jun-Lin Liu, Waseem Hassan, Lu-Lu Wang, Fang-Rong Yan, Jing Shang

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

9 citing papers in PubMed, 28 citations in OpenAlex.

  1. Review
  2. Article
  3. Chemometric Discrimination ofFoods (Basel, Switzerland) · 2023
    Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. 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.

Lin Ding1] National Center for Drug Screening & State Key Laboratory of Natural Medicines, China Pharmaceutical University, Jiangsu Province, 210009, P. R. China [2].
Jun-Lin Liu1] Research Center of Biostatistics and Computational Pharmacy, China Pharmaceutical University, Jiangsu Province, 210009, P. R. China [2].
Waseem HassanNational Center for Drug Screening & State Key Laboratory of Natural Medicines, China Pharmaceutical University, Jiangsu Province, 210009, P. R. China.
Lu-Lu WangNational Center for Drug Screening & State Key Laboratory of Natural Medicines, China Pharmaceutical University, Jiangsu Province, 210009, P. R. China.
Fang-Rong YanResearch Center of Biostatistics and Computational Pharmacy, China Pharmaceutical University, Jiangsu Province, 210009, P. R. China.
Jing ShangNational Center for Drug Screening & State Key Laboratory of Natural Medicines, China Pharmaceutical University, Jiangsu Province, 210009, P. R. China.
China Pharmaceutical University · CNNational Center for Drug Screening · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

To investigate a possible methodology of exploiting herbal medicine and design polytherapy for the treatment of non-alcoholic fatty liver disease (NAFLD), we have made use of Cichorium glandulosum Boiss et Huet (CG), a traditional Chinese herbal medicine that has been proven to be effective in treating hepatic diseases. Here, we report that the extract of CG effectively reduced lipid accumulation under conditions of lipid overloading in vivo and in vitro (in a rat high-fat diet model and a hepG2 cell model of free fatty acid treatment). CG extract also protected hepatocytes from injury and inflammation to aid its lipid-lowering properties (in a rat high-fat diet model and a L02 cell model of acetaminophen treatment). Serum chemistry analysis accompanied by in vitro drug screening confirmed that CG-4, CG-10 and CG-14 are the lipo-effective components of CG. Western blotting analysis revealed that these components can regulate key lipid targets at the molecular level, including CD36, FATP5 and PPAR-α, thus the lipid oxidation and lipid absorption pathways. Finally, we adopted the experimental design and statistical method to calculate the best combination proportion (CG-4: CG-10: CG-14 = 2.065: 1.782: 2.153) to optimize its therapeutic effect.

Indexed as

AnimalsCD36 AntigensCell Line, TumorDiet, High-FatFatty Acid Transport ProteinsHepatocytesHep G2 CellsHerbal MedicineHumansLipidsMaleNon-alcoholic Fatty Liver DiseasePhytotherapyPlant ExtractsPPAR alphaRatsCD36 AntigensFatty Acid Transport ProteinsLipidsPlant ExtractsPPAR alpha

Identifiers

PMID24797163
PMCPMC4010933
OpenAlexW2052187375

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.