Evidence map›Paper›PMID 22754327›Full record

ArticleInternational journal of molecular sciences2012

Ginsenoside Rg3 reduces lipid accumulation with AMP-Activated Protein Kinase (AMPK) activation in HepG2 cells.

Seohyun Lee, Mak-Soon Lee, Chong-Tai Kim, In-Hwan Kim, Yangha Kim

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
3.4field-weighted citation impact, top 7% 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

41 citing papers in PubMed, 81 citations in OpenAlex.

  1. Trial
  2. Review
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  5. Review
  6. [Protective Effect of Ginsenoside Rg3 on Lipopolysaccharide-Induced Neuronal-Galial Interaction Injury Model].Sichuan da xue xue bao. Yi xue ban = Journal of Sichuan University. Medical science edition · 2024
    Article
  7. Review
  8. Review
  9. The impact of the administration of red ginseng (Frontiers in veterinary science · 2024
    Article
  10. Article
  11. Review
  12. Article
  13. Article
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  16. Review
  17. Article
  18. Effect ofFrontiers in pharmacology · 2020
    Review
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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 1 country.

Seohyun LeeDepartment of Nutritional Science and Food Management, Ewha Womans University, Seoul 120-750, Korea.
Mak-Soon LeeDepartment of Nutritional Science and Food Management, Ewha Womans University, Seoul 120-750, Korea.
Chong-Tai KimFood Bio-Nano Research Group, Korea Food Research Institute, Seongnam, Gyeonggi 463-746, Korea.
In-Hwan KimDepartment of Food and Nutrition, College of Health Sciences, Korea University, Seoul 136-703, Korea.
Yangha KimDepartment of Nutritional Science and Food Management, Ewha Womans University, Seoul 120-750, Korea.ORCID 0000-0002-7280-7597
Ewha Womans University · KRKorea Food Research Institute · KRKorea University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cardiovascular disease (CVD) is one of the main causes of mortality worldwide, and dyslipidemia is a major risk factor for CVD. Ginseng has been widely used in the clinic to treat CVD. Ginsenoside Rg3, one of the major active components of ginseng, has been reported to exhibit antiobesity, antidiabetic, and cardioprotective effects. However, the effect of ginsenoside Rg3 on hepatic lipid metabolism remains unclear. Therefore, we investigated whether ginsenoside Rg3 would regulate hepatic lipid metabolism with AMP-activated protein kinase (AMPK) activation in HepG2 cells. Ginsenoside Rg3 significantly reduced hepatic cholesterol and triglyceride levels. Furthermore, ginsenoside Rg3 inhibited expression of sterol regulatory element binding protein-2 (SREBP-2) and 3-hydroxy-3-methyl glutaryl coenzyme A reductase (HMGCR). Ginsenoside Rg3 increased activity of AMPK, a major regulator of energy metabolism. These results suggest that ginsenoside Rg3 reduces hepatic lipid accumulation with inhibition of SREBP-2 and HMGCR expression and stimulation of AMPK activity in HepG2 cells. Therefore, ginsenoside Rg3 may be beneficial as a food ingredient to lower the risk of CVD by regulating dyslipidemia.

Indexed as

AMP-Activated Protein KinasesEnzyme ActivationGinsenosidesHep G2 CellsHumansLipid MetabolismLiverPanaxAMP-Activated Protein Kinasesginsenoside Rg3GinsenosidesAMPKCardiovascular disease (CVD)cholesterolginsenoside Rg3HMGCRSREBP-2triglyceride

Identifiers

PMID22754327
PMCPMC3382760
OpenAlexW1993142992

What OpenQuestion holds

Textmetadata
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.