Li Shu-Yuan, Chang Cui-Qing, Ma Fu-Ying, Yu Chang-Long
Division of Nutrition and Biochemistry, Institute of Sports Medicine, Third Hospital, Peking University, Beijing 100191, China.
Biomed Environ Sci. 2009 Apr;22(2):122-9. doi: 10.1016/S0895-3988(09)60034-9.
To examine the effects of chlorogenic acid (CGA) on lipid and glucose metabolism under a high dietary fat burden and to explore the possible role of peroxisome proliferator-activated receptor-alpha (PPAR-alpha) in these effects.
Twenty male golden hamsters were randomly divided into CGA treatment group (n=10, given peritoneal injection of CGA solution prepared with PBS, 80 mg CGA/kg body weight daily), and control group (n=10, given PBS i.p. at the average volume of the treatment group). Animals in both groups were given 15% high fat diet. Eight weeks after treatment with CGA, the level of biochemical parameters in fasting serum and tissues and the expression of hepatic mRNA and protein PPAR-alpha were determined.
Eight weeks after treatment with CGA, the levels of fasting serum triglyceride (TG), free fatty acid (FFA), total cholesterol (TC), low density lipoprotein cholesterol (LDL-C), high density lipoprotein cholesterol (HDL-C), glucose (FSG), and insulin (FSI) were significantly lower in the GGA treatment group than in the control group. CGA also led to higher activity of hepatic lipase (HL), lower contents of TG and FFA in liver, and lower activity of lipoprotein lipase (LPL) in skeletal muscle. Furthermore, CGA significantly elevated significantly elevated the expression level of mRNA and protein expression in hepatic PPAR-alpha.
CGA can modify lipids and glucose metabolism, which may be attributed to PPAR-alpha facilitated lipid clearance in liver and improved insulin sensitivity.
研究绿原酸(CGA)在高膳食脂肪负荷下对脂质和葡萄糖代谢的影响,并探讨过氧化物酶体增殖物激活受体α(PPAR-α)在这些影响中可能发挥的作用。
将20只雄性金黄仓鼠随机分为CGA治疗组(n = 10,腹腔注射用PBS配制的CGA溶液,每日80 mg CGA/kg体重)和对照组(n = 10,腹腔注射与治疗组平均体积相同的PBS)。两组动物均给予15%的高脂饮食。CGA治疗8周后,测定空腹血清和组织中的生化参数水平以及肝脏中PPAR-α的mRNA和蛋白表达。
CGA治疗8周后,CGA治疗组空腹血清甘油三酯(TG)、游离脂肪酸(FFA)、总胆固醇(TC)、低密度脂蛋白胆固醇(LDL-C)、高密度脂蛋白胆固醇(HDL-C)、葡萄糖(FSG)和胰岛素(FSI)水平均显著低于对照组。CGA还导致肝脏脂肪酶(HL)活性升高,肝脏中TG和FFA含量降低,骨骼肌中脂蛋白脂肪酶(LPL)活性降低。此外,CGA显著提高了肝脏PPAR-α的mRNA表达水平和蛋白表达水平。
CGA可改善脂质和葡萄糖代谢,这可能归因于PPAR-α促进肝脏脂质清除和提高胰岛素敏感性。