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Combined Beneficial Effect of Genistein and Atorvastatin on Adipogenesis in 3T3-L1 Adipocytes
- Source :
- Biomolecules, Volume 11, Issue 7, Biomolecules, Vol 11, Iss 1052, p 1052 (2021)
- Publication Year :
- 2021
- Publisher :
- MDPI AG, 2021.
-
Abstract
- Genistein (4,5,7-trihydroxyisoflavone) is abundant in various dietary vegetables, especially soybeans, and is known to have not only an estrogenic effect but also an antiadipogenic effect. Atorvastatin (dihydroxy monocarboxylic acid) is a statin used to prevent heart disease. Although genistein and atorvastatin have been reported to possess antiadipogenic effects, their combined effects are still unclear. The aim of the current study was to explore whether the combination of genistein and atorvastatin at low concentrations significantly suppresses adipogenesis in a murine preadipocyte cell line (3T3-L1) compared to treatment with genistein or atorvastatin alone. Our results showed that cotreatment with 50 µM genistein and 50 nM atorvastatin significantly suppressed preadipocyte differentiation, whereas when each compound was used alone, there was no inhibitory effect. Additionally, cotreatment with genistein and atorvastatin significantly downregulated adipogenic marker proteins, including mitogen-activated protein kinases (MAPKs), peroxisome proliferator-activated receptor γ (PPARγ), CCAAT/enhancer-binding protein alpha (C/EBPα), glucocorticoid receptor (GR), and CCAAT/enhancer-binding protein β (C/EBPβ). This is the first evidence of the combined antiadipogenic effects of genistein and atorvastatin. Although additional experiments are required, combinational treatment with genistein and atorvastatin may be an alternative treatment for menopause-associated lipid metabolic disorders and obesity.
- Subjects :
- 0301 basic medicine
Statin
medicine.drug_class
adipocytes
Atorvastatin
Genistein
Pharmacology
Microbiology
Biochemistry
Article
adipogenesis
genistein
Mice
03 medical and health sciences
chemistry.chemical_compound
Receptors, Glucocorticoid
0302 clinical medicine
Glucocorticoid receptor
3T3-L1 Cells
medicine
Animals
heterocyclic compounds
cardiovascular diseases
Receptor
Molecular Biology
Chemistry
Kinase
nutritional and metabolic diseases
Cell Differentiation
Drug Synergism
3T3-L1
atorvastatin
QR1-502
PPAR gamma
030104 developmental biology
Adipogenesis
030220 oncology & carcinogenesis
CCAAT-Enhancer-Binding Proteins
lipids (amino acids, peptides, and proteins)
Mitogen-Activated Protein Kinases
medicine.drug
Subjects
Details
- ISSN :
- 2218273X
- Volume :
- 11
- Database :
- OpenAIRE
- Journal :
- Biomolecules
- Accession number :
- edsair.doi.dedup.....0d3b4005f0029a9b6bcbb805a215be91
- Full Text :
- https://doi.org/10.3390/biom11071052