Engineering Laboratory for National Healthcare Theories and Products of Yunnan Province, College of Pharmaceutical Science, Yunnan University of Traditional Chinese Medicine, No. 1076 Yuhua Road, Chenggong District, Kunming 650500, Yunnan, China.
Guangdong Pharmaceutical University, Guangzhou 510006, China.
Fitoterapia. 2018 Mar;125:208-216. doi: 10.1016/j.fitote.2017.11.018. Epub 2017 Nov 21.
The leaves of Ilex Kudingcha, locally named "Kudingcha" in China, has been traditionally applied for treating obesity. Studies have demonstrated that the ethanol extract of Ilex kudingcha have anti-adipogenic effects. However, the constituent which was responsible for its anti-obesity and its underlying molecular mechanism has not yet been elucidated. This research explored the anti-obesity effect of kudinoside-D which was a main natural component of triterpenoid saponin from the ethanol extract of Ilex kudingcha, on lipid accumulation and the potential mechanism of action of adipogenesis in 3T3-L1 adipocytes. The adipocytes were treated with various concentrations of kudinoside D (0 to 40μM) during differentiation. The image-based Oil Red O staining analyses revealed that KD-D, dose dependently reduced cytoplasmic lipid droplet in 3T3-L1 adipocytes with the IC is 59.49μM. Meanwhile, major adipogenic transcription factor peroxisome proliferator-activated receptor γ (PPARγ), CCAAT/enhancer binding protein-α (C/EBPα) and sterol regulatory element-binding protein 1c (SREBP-1c) were significantly repressed as well as their target genes. The phosphorylation of AMP-activated protein kinase (AMPK) and its downstream target phosphorylated-acetyl CoA carboxylase (ACC) expression were also increased. In addition, the inhibitory effects of KD-D on the expressions of PPARγ and C/EBPα were weakened when cells were cotreated with AMPK inhibitor Compound C. These results indicated KD-D exerts anti-adipogenic effects through modulation of adipogenic transcription factors via AMPK signaling pathway. And the current findings demonstrated that KD-D was a potential therapeutic candidate for alleviating obesity and hyperlipidemia.
中国当地名为“苦丁茶”的冬青叶,历来被用于治疗肥胖症。研究表明,冬青苦丁茶的乙醇提取物具有抗脂肪生成作用。然而,负责其抗肥胖作用及其潜在分子机制的成分尚未阐明。本研究探索了冬青苦丁茶乙醇提取物中主要天然成分——三萜皂苷的苦丁苷-D 对 3T3-L1 脂肪细胞中脂肪积累的抗肥胖作用及其潜在作用机制。将脂肪细胞用不同浓度的苦丁苷-D(0 至 40μM)在分化过程中处理。基于图像的油红 O 染色分析显示,KD-D 呈浓度依赖性地减少 3T3-L1 脂肪细胞中的细胞质脂滴,IC 为 59.49μM。同时,主要的脂肪生成转录因子过氧化物酶体增殖物激活受体 γ(PPARγ)、CCAAT/增强子结合蛋白-α(C/EBPα)和固醇调节元件结合蛋白 1c(SREBP-1c)也被显著抑制,其靶基因也是如此。AMP 激活的蛋白激酶(AMPK)及其下游靶标磷酸化乙酰辅酶 A 羧化酶(ACC)的磷酸化也增加。此外,当细胞用 AMPK 抑制剂复合物 C 共处理时,KD-D 对 PPARγ 和 C/EBPα 表达的抑制作用减弱。这些结果表明,KD-D 通过 AMPK 信号通路调节脂肪生成转录因子发挥抗脂肪生成作用。并且目前的研究结果表明,KD-D 是缓解肥胖和高血脂的潜在治疗候选药物。