Effects of Lonicera caerulea extract on adipocyte differentiation and adipogenesis in 3T3-L1 cells and mouse adipose-derived stem cells (MADSCs)
- Author:
Miey PARK
1
;
Changho LEE
;
Hae Jeung LEE
Author Information
- Publication Type:Original Article
- Keywords: Lonicera caerulea; preadipocyte; anti-obesity; lipid accumulation
- MeSH: 3T3-L1 Cells; Adipocytes; Adipogenesis; Animals; Blotting, Western; Cardiovascular Diseases; Cell Survival; China; Japan; Lipid Droplets; Lonicera; Medicine, Traditional; Mice; Minerals; Miners; Non-alcoholic Fatty Liver Disease; Obesity; Peroxisomes; Polyphenols; Real-Time Polymerase Chain Reaction; RNA, Messenger; Russia; Stem Cells; Sterol Regulatory Element Binding Protein 1; Vitamins
- From:Journal of Nutrition and Health 2019;52(1):17-25
- CountryRepublic of Korea
- Language:Korean
- Abstract: PURPOSE: Obesity is a major health problem of global significance because it is clearly associated with an increased risk of health problems, such as nonalcoholic fatty liver disease (NAFLD), diabetes, cardiovascular diseases, and cancer. Lonicera caerulea (LC) originates from high mountains or wet areas and has been used as a traditional medicine in northern Russia, China, and Japan. LC contains a range of bioactive constituents, such as vitamins, minerals, and polyphenols. This study examined the anti-obesity effects of LC during differentiation in preadipocytes. METHODS: The cell viability assay was performed after the differentiation of 3T3-L1 cells for 7 days. Oil Red O staining was used to visualize the changes in lipid droplets in 3T3-L1 cells and mouse adipose-derived stem cells (MADSCs). The mRNA expression of obesity-related genes was determined by quantitative real-time PCR. RESULTS: According to the results of Oil Red O staining, the lipid levels and size of lipid droplets in the adipocytes were reduced and the LC extract (LCE, 0.25–1 mg/mL) markedly inhibited adipogenesis in a dose-dependent manner. The treatment of LCE also decreased the mRNA expression of peroxisome proliferator-activated receptor γ (PPARγ), CCAAT/enhancer binding protein-α (C/EBPα), and sterol regulatory element binding protein 1 (SREBP1) in 3T3-L1 cells. Western blot analysis showed that the PPARγ, C/EBPα, and SREBP1 protein levels in both 3T3-L1 and MADSC were reduced in a dose-dependent manner. CONCLUSION: These results suggest that LCE can inhibit adipogenic differentiation through the regulation of adipogenesis-related markers.
