Xie Jing, Wang Yan, Jiang Wei-Wei, Luo Xuan-Fei, Dai Tian-Yi, Peng Lei, Song Shuang, Li Ling-Fei, Tao Liang, Shi Chong-Ying, Hao Ruo-Shi, Xiao Rong, Tian Yang, Sheng Jun
Yunnan Provincial Key Laboratory of Biological Big Data, Yunnan Agricultural University, Kunming, China.
College of Biological Big Data, Yunnan Agricultural University, Kunming, China.
Front Pharmacol. 2018 Dec 18;9:1447. doi: 10.3389/fphar.2018.01447. eCollection 2018.
In recent years, obesity has become a key factor affecting human health. Lam. is a perennial tropical deciduous tree, which is widely used in human medicine due to its nutritional and unique medicinal value. It has a cholesterol-lowering effect, but its mechanism of action is unclear. In this study, we elucidated the inhibitory effect of leaf petroleum ether extract (MOPEE) on lipid accumulation by and experiments, and we described its mechanism of action. MOPEE suppressed adipogenesis in 3T3-L1 adipocytes in a dose-dependent manner and had no effect on cell viability at doses up to 400 μg/ml. Furthermore, MOPEE (400 μg/ml) significantly downregulated the expression of adipogenesis-associated proteins [peroxisome proliferator-activated receptor γ (PPARγ), CCAAT/enhancer-binding proteins α and β (C/EBPα and C/EBPβ), and fatty acid synthase (FAS)] and upregulated the expression of a lipolysis-associated protein [hormone-sensitive lipase (HSL)] in 3T3-L1 adipocytes. Additionally, MOPEE (400 μg/ml) significantly increased the degree of phosphorylation of AMP-activated protein kinase α (AMPKα) and acetyl-CoA carboxylase (ACC). An AMPK inhibitor reversed the MOPEE-induced activation of AMPKα and ACC in 3T3-L1 adipocytes. Animal experiments showed that, in high-fat diet (HFD) mice, MOPEE [0.5 g/kg body weight (BW)] effectively decreased BW; relative epididymal, perirenal, and mesenteric fat weight and fat tissue size; and hepatic fat accumulation. Furthermore, MOPEE markedly reduced the serum levels of total cholesterol (TC), low-density lipoprotein cholesterol (LDL-C), and aspartate aminotransferase (AST). Moreover, MOPEE significantly downregulated the expression of adipogenesis-associated proteins (PPARγ and FAS) and upregulated the expression of a lipolysis-associated protein [adipose triglyceride lipase (ATGL)] in HFD mice hepatic and epididymal fat tissue. Additionally, MOPEE markedly increased the degree of phosphorylation of AMPKα and ACC in HFD mice hepatic and epididymal fat tissue. Following ultrahigh-performance liquid chromatography quadrupole time-of-flight tandem mass spectrometry (UPLC-QTOF-MS/MS) analysis, three phytocompounds (isoquercitrin, chrysin-7-glucoside, and quercitrin) were identified as compounds with relatively high levels in MOPEE. Among them, quercitrin showed excellent fat accumulation inhibitory activity, and the three compounds had synergistic effects in inhibiting adipogenesis. Taken together, MOPEE inhibits fat accumulation by inhibiting the adipogenesis and promoting the lipolysis, and this process is related to AMPK activation.
近年来,肥胖已成为影响人类健康的关键因素。榄李是一种多年生热带落叶乔木,因其营养和独特的药用价值而被广泛应用于人类医学。它具有降胆固醇作用,但其作用机制尚不清楚。在本研究中,我们通过体外和体内实验阐明了叶石油醚提取物(MOPEE)对脂质积累的抑制作用,并描述了其作用机制。MOPEE以剂量依赖的方式抑制3T3-L1脂肪细胞的脂肪生成,在高达400μg/ml的剂量下对细胞活力没有影响。此外,MOPEE(400μg/ml)显著下调3T3-L1脂肪细胞中脂肪生成相关蛋白[过氧化物酶体增殖物激活受体γ(PPARγ)、CCAAT/增强子结合蛋白α和β(C/EBPα和C/EBPβ)以及脂肪酸合酶(FAS)]的表达,并上调脂肪分解相关蛋白[激素敏感性脂肪酶(HSL)]的表达。此外,MOPEE(400μg/ml)显著增加了AMP激活蛋白激酶α(AMPKα)和乙酰辅酶A羧化酶(ACC)的磷酸化程度。AMPK抑制剂可逆转MOPEE诱导的3T3-L1脂肪细胞中AMPKα和ACC的激活。动物实验表明,在高脂饮食(HFD)小鼠中,MOPEE[0.5g/kg体重(BW)]有效地降低了体重;附睾、肾周和肠系膜相对脂肪重量以及脂肪组织大小;以及肝脏脂肪积累。此外,MOPEE显著降低了血清总胆固醇(TC)、低密度脂蛋白胆固醇(LDL-C)和天冬氨酸转氨酶(AST)水平。此外,MOPEE显著下调HFD小鼠肝脏和附睾脂肪组织中脂肪生成相关蛋白(PPARγ和FAS)的表达,并上调脂肪分解相关蛋白[脂肪甘油三酯脂肪酶(ATGL)]的表达。此外,MOPEE显著增加了HFD小鼠肝脏和附睾脂肪组织中AMPKα和ACC的磷酸化程度。经过超高效液相色谱四极杆飞行时间串联质谱(UPLC-QTOF-MS/MS)分析,鉴定出三种植物化合物(异槲皮苷、白杨素-7-葡萄糖苷和槲皮苷)为MOPEE中含量相对较高的化合物。其中,槲皮苷表现出优异的脂肪积累抑制活性,这三种化合物在抑制脂肪生成方面具有协同作用。综上所述,MOPEE通过抑制脂肪生成和促进脂肪分解来抑制脂肪积累,这一过程与AMPK激活有关。