Korea Cancer Preventive Material Development Research Center, College of Korean Medicine, Kyung Hee University, 1 Hoegi-dong, Dongdaemun-gu, Seoul 130-701, Republic of Korea.
J Agric Food Chem. 2015 Aug 19;63(32):7270-6. doi: 10.1021/acs.jafc.5b01954. Epub 2015 Jul 29.
Rhus verniciflua Stokes has been used as a traditional medicine and food supplement in Korea. In the present study, fermented R. verniciflua Stokes extract (FRVE), an allergen-free extract of R. verniciflua Stokes fermented with the yeast Saccharomyces carlsbergensis, was assessed for its lipid-lowering potential in an in vitro non-alcoholic fatty liver disease model. FRVE markedly suppressed lipid accumulation and intracellular triglycerides (TGs) in the presence of oleic acid (OA). Additionally, FRVE decreased both mRNA and protein levels of lipid-synthesis- and cholesterol-metabolism-related factors, such as sterol regulatory element-binding protein-1 (SREBP-1), fatty acid synthase (FAS), glycerol-3-phosphate acyltransferase (GPAT), and 3-hydroxy-3-methylglutaryl coenzyme A reductase (HMGCR), in OA-induced HepG2 cells. Moreover, FRVE activated low-density lipoprotein receptor (LDLR), AMP-activated protein kinase (AMPK), and fatty acid oxidation-related factors peroxisome proliferator activated receptor α (PPARα) and carnitine palmitoyltransferase 1 (CPT-1). Further, the AMPK inhibitor compound C suppressed the increased expression of AMPK phosphorylation induced by FRVE. Phenolics and cosanols in FRVE increased the phosphorylation of AMPK and decreased that of SREBP-1. Taken together, our findings suggest that FRVE has antilipogenic potential in non-alcoholic fatty livers via AMPK upregulation.
漆树已被用作韩国传统药物和食品补充剂。在本研究中,漆树发酵提取物(FRVE)是一种不含过敏原的漆树发酵提取物,它是用酵母酿酒酵母发酵而成的,在体外非酒精性脂肪肝疾病模型中评估了其降低血脂的潜力。FRVE 显著抑制了油酸(OA)存在下的脂质积累和细胞内三酰基甘油(TGs)。此外,FRVE 降低了脂合成和胆固醇代谢相关因子的 mRNA 和蛋白水平,如固醇调节元件结合蛋白-1(SREBP-1)、脂肪酸合酶(FAS)、甘油-3-磷酸酰基转移酶(GPAT)和 3-羟-3-甲基戊二酰辅酶 A 还原酶(HMGCR),在 OA 诱导的 HepG2 细胞中。此外,FRVE 激活了低密度脂蛋白受体(LDLR)、AMP 激活的蛋白激酶(AMPK)和脂肪酸氧化相关因子过氧化物酶体增殖物激活受体α(PPARα)和肉碱棕榈酰转移酶 1(CPT-1)。此外,AMPK 抑制剂化合物 C 抑制了 FRVE 诱导的 AMPK 磷酸化的增加。FRVE 中的酚类和角鲨烯增加了 AMPK 的磷酸化,降低了 SREBP-1 的磷酸化。总之,我们的研究结果表明,FRVE 通过上调 AMPK 具有抗非酒精性脂肪肝的作用。