Park Hyo Jin, Kim Hye-Jin, Kim Sang Ryong, Choi Myung-Sook, Jung Un Ju
Department of Food Science and Nutrition, Kyungpook National University, 1370 Sankyuk Dong Puk-ku, 702-701 Daegu, Republic of Korea.
Food R&D, CJ Cheiljedang Corp, 152-051 Seoul, Republic of Korea.
J Nutr Biochem. 2017 Mar;41:137-141. doi: 10.1016/j.jnutbio.2016.12.016. Epub 2017 Jan 9.
This study investigated the biological and molecular mechanisms underlying the antiobesity effect of omija fruit ethanol extract (OFE) in mice fed a high-fat diet (HFD). C57BL/6J mice were fed an HFD (20% fat, w/w) with or without OFE (500 mg/kg body weight) for 16 weeks. Dietary OFE significantly increased brown adipose tissue weight and energy expenditure while concomitantly decreasing white adipose tissue (WAT) weight and adipocyte size by up-regulating the expression of brown fat-selective genes in WAT. OFE also improved hepatic steatosis and dyslipidemia by enhancing hepatic fatty acid oxidation-related enzymes activity and fecal lipid excretion. In addition to steatosis, OFE decreased the expression of pro-inflammatory genes in the liver. Moreover, OFE improved glucose tolerance and lowered plasma glucose, insulin and homeostasis model assessment of insulin resistance, which may be linked to decreases in the activity of hepatic gluconeogenic enzymes and the circulating level of gastric inhibitory polypeptide. These findings suggest that OFE may protect against diet-induced adiposity and related metabolic disturbances by controlling brown-like transformation of WAT, fatty acid oxidation, inflammation in the liver and fecal lipid excretion. Improved insulin resistance may be also associated with its antiobesity effects.
本研究调查了五味子果实乙醇提取物(OFE)对高脂饮食(HFD)喂养小鼠的抗肥胖作用的生物学和分子机制。将C57BL/6J小鼠喂食含或不含OFE(500毫克/千克体重)的高脂饮食(20%脂肪,w/w)16周。饮食中的OFE显著增加棕色脂肪组织重量和能量消耗,同时通过上调白色脂肪组织(WAT)中棕色脂肪选择性基因的表达,降低白色脂肪组织(WAT)重量和脂肪细胞大小。OFE还通过增强肝脏脂肪酸氧化相关酶活性和粪便脂质排泄,改善肝脂肪变性和血脂异常。除脂肪变性外,OFE还降低了肝脏中促炎基因的表达。此外,OFE改善了葡萄糖耐量,降低了血浆葡萄糖、胰岛素和胰岛素抵抗的稳态模型评估,这可能与肝脏糖异生酶活性的降低和胃抑制多肽的循环水平有关。这些发现表明,OFE可能通过控制WAT的棕色样转化、脂肪酸氧化、肝脏炎症和粪便脂质排泄,预防饮食诱导的肥胖和相关代谢紊乱。胰岛素抵抗的改善也可能与其抗肥胖作用有关。