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Water Extracts of Immature Rubus coreanus Regulate Lipid Metabolism in Liver Cells
- Source :
- Biological and Pharmaceutical Bulletin. 35:1907-1913
- Publication Year :
- 2012
- Publisher :
- Pharmaceutical Society of Japan, 2012.
-
Abstract
- Hyperlipidemia is a major contributor for atherosclerosis and hypolipidemic drugs such as statin are highly prescribed to treat elevated lipid level in plasma. Rubus coreanus, which is widely cultivated in south eastern Asia, have been reported to show significant cholesterol lowering action in hyperlipidemic subjects. Our objective was to determine the cellular effect of Rubus coreanus extract (RCE) on cholesterol biosynthesis in human hepatic cells (HepG2) and to elucidate the molecular mechanism by which it causes change in cholesterol metabolism. RCE treatment lowered cholesterol biosynthesis as well as secretion from HepG2 cells. This effect was associated with lowering the release of apolipoproteins from hepatic cells. RCE treatment also showed an increase in phosphorylation of foxhead box protein 01 (FoXo-1) and 5-adenosine monophosphate-activated protein kinase (AMPK), thus lowering expression of phosphoenolpyruvate carboxykinase (PEPCK) and G6Pase, which might be a major pathway for cholesterol biosynthesis inhibition. Apart from this; RCE also lowered sterol regulatory element-binding protein-1 (SREBP-1) expression in HepG2 cells, showing a long term regulation of cholesterol biosynthesis activity. These results indicate that one of the anti-hyperlipidemic actions of RCE is due to inhibition of cholesterol biosynthesis in hepatic cells and provides first documentation of a hypolipidemic bio-molecular action of Rubus coreanus.
- Subjects :
- Pharmacology
Statin
biology
medicine.drug_class
Cholesterol
Liver cytology
Pharmaceutical Science
Rubus coreanus
FOXO1
Lipid metabolism
General Medicine
biology.organism_classification
Sterol
chemistry.chemical_compound
Biochemistry
chemistry
medicine
Hepatic stellate cell
lipids (amino acids, peptides, and proteins)
Subjects
Details
- ISSN :
- 13475215 and 09186158
- Volume :
- 35
- Database :
- OpenAIRE
- Journal :
- Biological and Pharmaceutical Bulletin
- Accession number :
- edsair.doi...........54c1ea5836cb548cd673fb61b8f8b48f
- Full Text :
- https://doi.org/10.1248/bpb.b12-00022