Evidence map›Paper›PMID 29254285›Full record

ArticleClinical and molecular hepatology2018

Picroside II attenuates fatty acid accumulation in HepG2 cells via modulation of fatty acid uptake and synthesis.

Hiteshi Dhami-Shah, Rama Vaidya, Shobha Udipi, Srividhya Raghavan, Shiny Abhijit, Viswanathan Mohan, Muthuswamy Balasubramanyam, Ashok Vaidya

Open access · goldAbstract read
In one paragraph

Article in Clinical and molecular hepatology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 1 pooled it
1.2field-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

18 citing papers in PubMed, 1 synthesis or guideline pooled it, 31 citations in OpenAlex.

  1. The Green Path to Liver Health: Herbal Solutions for Non-alcoholic Steatohepatitis.Cardiovascular & hematological disorders drug targets · 2025
    Pooled it
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Review
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

8 authors at 2 institutions in 1 country.

Hiteshi Dhami-ShahDivision of Endocrine and Metabolic Disorders, Kasturba Health Society, Medical Research Centre, Mumbai, India.ORCID 0000-0002-6092-3873
Rama VaidyaDivision of Endocrine and Metabolic Disorders, Kasturba Health Society, Medical Research Centre, Mumbai, India.
Shobha UdipiDivision of Endocrine and Metabolic Disorders, Kasturba Health Society, Medical Research Centre, Mumbai, India.
Srividhya RaghavanDepartment of Cell and Molecular Biology, Madras Diabetes Research Foundation, Chennai, India.
Shiny AbhijitDepartment of Cell and Molecular Biology, Madras Diabetes Research Foundation, Chennai, India.
Viswanathan MohanDepartment of Cell and Molecular Biology, Madras Diabetes Research Foundation, Chennai, India.
Muthuswamy BalasubramanyamDepartment of Cell and Molecular Biology, Madras Diabetes Research Foundation, Chennai, India.
Ashok VaidyaDivision of Endocrine and Metabolic Disorders, Kasturba Health Society, Medical Research Centre, Mumbai, India.
Madras Diabetes Research Foundation · INKasturba Hospital · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND/

aimsHepatic steatosis is caused by an imbalance between free fatty acids (FFAs) uptake, utilization, storage, and disposal. Understanding the molecular mechanisms involved in FFAs accumulation and its modulation could drive the development of potential therapies for Nonalcoholic fatty liver disease. The aim of the current study was to explore the effects of picroside II, a phytoactive found in

methodsHepG2 cells were loaded with FFAs (oleic acid:palmitic acid/2:1) for 20 hours to mimic hepatic steatosis. The FFAs concentration achieving maximum fat accumulation and minimal cytotoxicity (500 μM) was standardized. HepG2 cells were exposed to the standardized FFAs concentration with and without picroside II pretreatment.

resultsPicroside II pretreatment inhibited FFAs-induced lipid accumulation by attenuating the expression of fatty acid transport protein 5, sterol regulatory element binding protein 1 and stearoyl CoA desaturase. Preatreatment with picroside II was also found to decrease the expression of forkhead box protein O1 and phosphoenolpyruvate carboxykinase.

conclusionsThese findings suggest that picroside II effectively attenuated fatty acid accumulation by decreasing FFAs uptake and lipogenesis. Picroside II also decreased the expression of gluconeogenic genes.

Indexed as

AnimalsCattleCinnamatesFatty AcidsFatty Acid Transport ProteinsForkhead Box Protein O1GluconeogenesisHep G2 CellsHumansIridoid GlucosidesLipid MetabolismLipogenesisSerum Albumin, BovineStearoyl-CoA DesaturaseSterol Regulatory Element Binding Protein 1CinnamatesFatty AcidsFatty Acid Transport ProteinsForkhead Box Protein O1Iridoid Glucosidespicroside IISerum Albumin, BovineStearoyl-CoA DesaturaseSterol Regulatory Element Binding Protein 1Nonalcoholic fatty liver diseasePicrorhiza kurroaPicroside IIReverse pharmacologySilibinin

Identifiers

PMID29254285
PMCPMC5875197
OpenAlexW2776703455

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.