Department of Clinical Dietetics & Human Nutrition, Faculty of Pharmaceutical Sciences, Josai University, Keyakidai, Sakado, Saitama 350-0295, Japan.
J Nutr Biochem. 2010 Jul;21(7):573-9. doi: 10.1016/j.jnutbio.2009.02.013. Epub 2009 May 15.
Although cholesterol plays various important roles in the body, when overconsumed, it causes atherosclerosis and results in ischemic heart disease. On the other hand, dietary fish oils contain n-3 fatty acids, such as eicosapentaenoic acid and docosahexaenoic acid, which prevent ischemic heart disease. This effect of n-3 fatty acids mainly results from the combined effects of inhibiting lipogenesis via a decrease of the mature form of sterol regulatory element-binding proteins (SREBPs) and stimulating fatty acid oxidation via peroxisome proliferator-activator receptor (PPAR) alpha activation in the liver. In this study, we examined the interactive effects on lipid metabolism of dietary 2% cholesterol (w/w) and 20% or 50% energy fish oil. In a safflower oil diet with 2% cholesterol, hepatic lipids accumulated. On the other hand, hepatic lipids did not accumulate in the fish oil diets with cholesterol. Furthermore, in the groups with fish oil energy ratios of 20%, the negative feedback control of cholesterol affected SREBP-2, and the actions of fish oil and cholesterol were equivalent, but this was not observed in the cases with fish oil energy ratios of 50%. The results of this study suggest that differences in lipid accumulation in the body are due to differences in lipid source and energy ratios which differentially impact the control of transcription factors by cholesterol.
尽管胆固醇在体内发挥着各种重要作用,但过量摄入时会导致动脉粥样硬化,并引发缺血性心脏病。另一方面,饮食中的鱼油含有 n-3 脂肪酸,如二十碳五烯酸和二十二碳六烯酸,可预防缺血性心脏病。n-3 脂肪酸的这种作用主要是由于通过减少固醇调节元件结合蛋白(SREBP)的成熟形式来抑制脂肪生成,以及通过过氧化物酶体增殖物激活受体(PPAR)α激活来刺激脂肪酸氧化的联合作用所致。在这项研究中,我们研究了饮食中 2%胆固醇(w/w)和 20%或 50%能量鱼油对脂质代谢的相互作用。在含有 2%胆固醇的红花油饮食中,肝脏中的脂质堆积。另一方面,在含有胆固醇的鱼油饮食中,肝脏中的脂质并未堆积。此外,在鱼油能量比为 20%的组中,胆固醇的负反馈控制影响了 SREBP-2,并且鱼油和胆固醇的作用相当,但在鱼油能量比为 50%的情况下则没有观察到这种情况。本研究结果表明,体内脂质堆积的差异是由于脂质来源和能量比的差异所致,这些差异会对胆固醇控制转录因子的作用产生不同的影响。