Yang Soo Jin, Park Na-Young, Lim Yunsook
Department of Food and Nutrition and Human Ecology Research Institute, Chonnam National University, Jeonnam 500-757, Korea.
Department of Food and Nutrition, Kyung Hee University, 26 Kyungheedae-ro, Dongdaemun-gu, Seoul 130-701, Korea.
Nutr Res Pract. 2014 Dec;8(6):613-7. doi: 10.4162/nrp.2014.8.6.613. Epub 2014 Nov 28.
BACKGROUND/OBJECTIVES: Adipogenesis is part of the cell differentiation process in which undifferentiated fibroblasts (pre-adipocytes) become mature adipocytes with the accumulation of lipid droplets and subsequent cell morphological changes. Several transcription factors and food components have been suggested to be involved in adipogenesis. The aim of this study was to determine whether mulberry leaf ethanol extract (MLEE) affects adipogenesis in 3T3-L1 adipocytes.
MATERIALS/METHODS: The 3T3-L1 adipocytes were treated with different doses of MLEE for 8 days starting 2 days post-confluence. Cell viability, fat accumulation, and adipogenesis-related factors including CCAAT-enhancer-binding protein alpha (C/EBPα), peroxisome proliferator-activated receptor gamma (PPARγ), PPARγ coactivator 1 alpha (PGC-1α), fatty acid synthase (FAS), and adiponectin were analyzed.
Results showed that MLEE treatments at 10, 25, 50, and 100 µg/ml had no effect on cell morphology and viability. Without evident toxicity, all MLEE treated cells had lower fat accumulation compared with control as shown by lower absorbances of Oil Red O stain. MLEE at 50 and 100 µg/ml significantly reduced protein levels of PPARγ, PGC-1α, FAS, and adiponectin in differentiated adipocytes. Furthermore, protein level of C/EBPα was significantly decreased by the treatment of 100 µg/ml MLEE.
These results demonstrate that MLEE treatment has an anti-adipogenic effect in differentiated adipocytes without toxicity, suggesting its potential as an anti-obesity therapeutic.
背景/目的:脂肪生成是细胞分化过程的一部分,在此过程中未分化的成纤维细胞(前脂肪细胞)通过脂滴积累和随后的细胞形态变化成为成熟的脂肪细胞。已有研究表明,多种转录因子和食物成分参与脂肪生成。本研究旨在确定桑叶乙醇提取物(MLEE)是否会影响3T3-L1脂肪细胞的脂肪生成。
材料/方法:在3T3-L1脂肪细胞汇合后2天开始,用不同剂量的MLEE处理8天。分析细胞活力、脂肪积累以及与脂肪生成相关的因子,包括CCAAT增强子结合蛋白α(C/EBPα)、过氧化物酶体增殖物激活受体γ(PPARγ)、PPARγ共激活因子1α(PGC-1α)、脂肪酸合酶(FAS)和脂联素。
结果显示,10、25、50和100μg/ml的MLEE处理对细胞形态和活力没有影响。在无明显毒性的情况下,与对照组相比,所有MLEE处理的细胞脂肪积累均较低,这通过油红O染色较低的吸光度得以体现。50和100μg/ml的MLEE显著降低了分化脂肪细胞中PPARγ、PGC-1α、FAS和脂联素的蛋白质水平。此外,100μg/ml的MLEE处理显著降低了C/EBPα的蛋白质水平。
这些结果表明,MLEE处理对分化的脂肪细胞具有抗脂肪生成作用且无毒性,表明其具有作为抗肥胖治疗药物的潜力。