Ahn Hyemyoung, Jeong Jeongho, Moyo Knowledge, Ryu Yungsun, Min Bokkee, Yun Seong Ho, Kim Hwa Yeon, Kim Wooki, Go Gwang-Woong
Department of Food and Nutrition, Kookmin University, Seoul 02707, Republic of Korea.
NOVAREX Co., Ltd., Life Science Institute, Ochang 28126, Republic of Korea.
J Microbiol Biotechnol. 2017 Nov 28;27(11):1925-1931. doi: 10.4014/jmb.1707.07030.
Korean red pine () bark extract, PineXol (PX), was investigated for its potential antioxidant and anti-inflammation effects in vitro. It was hypothesized that PX treatment (25-150 μg/ml) would reduce the lipid synthesis in HepG2 hepatocytes as well as lipid accumulation in 3T3-L1 adipocytes. Hepatocytes' intracellular triglycerides and cholesterol were decreased in the PX 150 μg/ml treatment group compared with the control ( < 0.05). Consequently, de novo lipogenic proteins (acetyl-CoA carboxylase 1, stearoyl-CoA desaturase 1, elongase of very long chain fatty acids 6, glycerol-3-phosphate acyltransferase 1, and sterol regulatory element-binding protein 1) were significantly decreased in hepatocytes by PX 150 μg/ml treatment compared with the control ( < 0.05). In differentiated 3T3-L1 adipocytes, the lipid accumulation was significantly attenuated by all PX treatments ( < 0.01). Regulators of adipogenesis, including CCAAT-enhancer-binding proteins alpha, peroxisome proliferator-activated receptor gamma, and perilipin, were decreased in PX 100 μg/ml treatment compared with the control ( < 0.05). In conclusion, PX might have anti-obesity effects by blocking hepatic lipogenesis and by inhibiting adipogenesis in adipocytes.
研究了韩国红松()树皮提取物PineXol(PX)在体外的潜在抗氧化和抗炎作用。研究假设,PX处理(25 - 150μg/ml)将减少HepG2肝细胞中的脂质合成以及3T3 - L1脂肪细胞中的脂质积累。与对照组相比,PX 150μg/ml处理组肝细胞内的甘油三酯和胆固醇降低(<0.05)。因此,与对照组相比,PX 150μg/ml处理使肝细胞中从头脂肪生成蛋白(乙酰辅酶A羧化酶1、硬脂酰辅酶A去饱和酶1、极长链脂肪酸延长酶6、甘油-3-磷酸酰基转移酶1和固醇调节元件结合蛋白1)显著降低(<0.05)。在分化的3T3 - L1脂肪细胞中,所有PX处理均显著减弱脂质积累(<0.01)。与对照组相比,PX 100μg/ml处理使脂肪生成调节因子,包括CCAAT增强子结合蛋白α、过氧化物酶体增殖物激活受体γ和脂滴包被蛋白减少(<0.05)。总之,PX可能通过阻断肝脏脂肪生成和抑制脂肪细胞中的脂肪生成而具有抗肥胖作用。