Kim Ji Hye, Kim Ok-Kyung, Yoon Ho-Geun, Park Jeongjin, You Yanghee, Kim Kyungmi, Lee Yoo-Hyun, Choi Kyung-Chul, Lee Jeongmin, Jun Woojin
Division of Food and Nutritional Science, Chonnam National University, Gwangju, Republic of Korea.
Research Institute for Human Ecology, Chonnam National University, Gwangju, Republic of Korea.
Food Nutr Res. 2016 Jan 27;60:30428. doi: 10.3402/fnr.v60.30428. eCollection 2016.
Even though Curcuma longa L. possesses various biological activities, it has strong flavor and taste, which decrease consumer palatability and limit industrial applications in food.
The present study investigates the effects of C. longa L. fermented with Aspergillus oryzae supplementation in 60% high-fat diet-induced obese rats measured by the activation of adipogenesis and lipolysis.
Rats were divided into four groups (n=6 per group) after 1 week of acclimatization: a normal diet group comprised rats fed the AIN76A rodent diet; a high-fat diet-induced obese group with rats fed a 60% high-fat diet; a Garcinia cambogia treated group (positive control) with rats fed a 60% high-fat diet with G. cambogia 500 g/kg body weight (b.w.)/day; and an fermented C. longa L. 50% ethanolic extract treated group (FCE50) with rats fed a 60% high-fat diet with FCE50 500 g/kg b.w./day. Each group received the appropriate vehicle or sample daily by gastric intubation for 12 weeks.
We found that FCE50 administration suppressed b.w. gain and reduced white adipose tissue weight, serum triglyceride (TG), and cholesterol in high-fat diet-induced obese rats. These results can be associated with the suppression of adipocyte differentiation and lipogenesis with a decrease in the mRNA expressions of fatty acid synthase, acetyl-CoA carboxylase, adipocyte protein 2, and lipoprotein lipase induced by FCE50 administration. In addition, FCE50 increased lipolysis and β-oxidation by up-regulating the expression of lipases such as adipose triglyceride lipase, hormone-sensitive lipase, adiponectin, and AMP-activated protein kinase.
These results suggest that FCE50 can be a candidate for the prevention of obesity via suppressing adipogenesis and promoting lipolysis.
尽管姜黄具有多种生物活性,但其具有强烈的风味和味道,这降低了消费者的适口性并限制了其在食品中的工业应用。
本研究通过测量脂肪生成和脂肪分解的激活情况,研究米曲霉发酵姜黄对60%高脂饮食诱导的肥胖大鼠的影响。
适应1周后,将大鼠分为四组(每组n = 6):正常饮食组大鼠喂食AIN76A啮齿动物饮食;高脂饮食诱导的肥胖组大鼠喂食60%高脂饮食;藤黄果治疗组(阳性对照)大鼠喂食60%高脂饮食并每日给予藤黄果500 g/kg体重;发酵姜黄50%乙醇提取物治疗组(FCE50)大鼠喂食60%高脂饮食并每日给予FCE50 500 g/kg体重。每组每天通过胃内插管接受适当的载体或样品,持续12周。
我们发现,给予FCE50可抑制高脂饮食诱导的肥胖大鼠的体重增加,降低白色脂肪组织重量、血清甘油三酯(TG)和胆固醇。这些结果可能与FCE50抑制脂肪细胞分化和脂肪生成有关,FCE50给药可使脂肪酸合酶、乙酰辅酶A羧化酶、脂肪细胞蛋白2和脂蛋白脂肪酶的mRNA表达降低。此外,FCE50通过上调脂肪甘油三酯脂肪酶、激素敏感性脂肪酶、脂联素和AMP激活蛋白激酶等脂肪酶的表达来增加脂肪分解和β氧化。
这些结果表明,FCE50可通过抑制脂肪生成和促进脂肪分解成为预防肥胖的候选药物。