Li Kai Kai, Liu Chuek Lun, Shiu Hoi Ting, Wong Hing Lok, Siu Wing Sum, Zhang Cheng, Han Xiao Qiang, Ye Chuang Xing, Leung Ping Chung, Ko Chun Hay
Institute of Chinese Medicine, The Chinese University of Hong Kong, Shatin, New Territories, Hong Kong SAR, China.
State Key Laboratory of Phytochemistry and Plant Resources in West China, The Chinese University of Hong Kong, Shatin, New Territories, Hong Kong SAR, China.
Sci Rep. 2016 Feb 1;6:20172. doi: 10.1038/srep20172.
Cocoa tea (Camellia ptilophylla) is a naturally decaffeinated tea plant. Previously we found that cocoa tea demonstrated a beneficial effect against high-fat diet induced obesity, hepatic steatosis, and hyperlipidemia in mice. The present study aimed to investigate the anti-adipogenic effect of cocoa tea in vitro using preadipocytes 3T3-L1. Adipogenic differentiation was confirmed by Oil Red O stain, qPCR and Western blot. Our results demonstrated that cocoa tea significantly inhibited triglyceride accumulation in mature adipocytes in a dose-dependent manner. Cocoa tea was shown to suppress the expressions of key adipogenic transcription factors, including peroxisome proliferator-activated receptor gamma (PPAR γ) and CCAAT/enhancer binding protein (C/EBP α). The tea extract was subsequently found to reduce the expressions of adipocyte-specific genes such as sterol regulatory element binding transcription factor 1c (SREBP-1c), fatty acid synthase (FAS), Acetyl-CoA carboxylase (ACC), fatty acid translocase (FAT) and stearoylcoenzyme A desaturase-1 (SCD-1). In addition, JNK, ERK and p38 phosphorylation were inhibited during cocoa tea inhibition of 3T3-L1 adipogenic differentiation. Taken together, this is the first study that demonstrates cocoa tea has the capacity to suppress adipogenesis in pre-adipocyte 3T3-L1 similar to traditional green tea.
可可茶(毛叶茶)是一种天然不含咖啡因的茶树。此前我们发现,可可茶对高脂饮食诱导的小鼠肥胖、肝脂肪变性和高脂血症具有有益作用。本研究旨在利用前脂肪细胞3T3-L1体外研究可可茶的抗脂肪生成作用。通过油红O染色、qPCR和蛋白质免疫印迹法确认脂肪生成分化。我们的结果表明,可可茶以剂量依赖的方式显著抑制成熟脂肪细胞中甘油三酯的积累。可可茶被证明可抑制关键脂肪生成转录因子的表达,包括过氧化物酶体增殖物激活受体γ(PPARγ)和CCAAT/增强子结合蛋白(C/EBPα)。随后发现茶提取物可降低脂肪细胞特异性基因的表达,如固醇调节元件结合转录因子1c(SREBP-1c)、脂肪酸合酶(FAS)、乙酰辅酶A羧化酶(ACC)、脂肪酸转运蛋白(FAT)和硬脂酰辅酶A去饱和酶-1(SCD-1)。此外,在可可茶抑制3T3-L1脂肪生成分化过程中,JNK、ERK和p38磷酸化受到抑制。综上所述,这是第一项证明可可茶具有与传统绿茶类似的抑制前脂肪细胞3T3-L1脂肪生成能力的研究。