Lin Mei-Huei, Lu Shao-Chun, Huang Po-Chao, Liu Young-Chau, Liu Shyun-Yeu
Department of Biotechnology, Chia Nan University of Pharmacy and Science, Tainan, Taiwan/ROC.
Ann Nutr Metab. 2004 Sep-Oct;48(5):321-8. doi: 10.1159/000081199. Epub 2004 Oct 1.
This study was designed to investigate the effects of the interaction between dietary (n-3) polyunsaturated fatty acids (PUFA) and different dietary cholesterol content on plasma and liver cholesterol in hamsters. Male Syrian hamsters consumed diets containing an incremental increase in dietary cholesterol content (0, 0.025, 0.05, 0.1 and 0.2%, w/w) with either (n-3) PUFA (21 g/100 g fatty acids) or (n-6) PUFA (37.4 g/100 g fatty acids) fat for 6 weeks. In hamsters fed the nonatherogenic diet (0 or 0.025% dietary cholesterol), very low density lipoprotein (VLDL)-cholesterol levels in the (n-3) PUFA group were not significantly different from those in the (n-6) PUFA group, and low density lipoprotein (LDL)-cholesterol levels in the (n-3) PUFA group were significantly lower than those in the (n-6) PUFA group. In contrast, in hamsters fed the atherogenic diet (0.1 or 0.2% dietary cholesterol), VLDL- and LDL-cholesterol levels in the (n-3) PUFA group were significantly higher than those in the (n-6) PUFA group, in a dose-dependent manner. When the hamsters were fed with 0, 0.025, 0.05, 0.1 or 0.2% (w/w) dietary cholesterol, high density lipoprotein (HDL) cholesterol concentration was significantly lower in the (n-3) PUFA group than those in the (n-6) PUFA group. Hepatic cholesteryl esters were significantly lower, while hepatic microsomal acyl-coenzyme A:cholesterol acyltransferase activity and VLDL-cholesteryl esters were significantly higher in hamsters fed (n-3) PUFA with the atherogenic diet (0.1 or 0.2% dietary cholesterol) than in those fed (n-6) PUFA with the atherogenic diet. Our results demonstrate that the amount of dietary cholesterol is an important factor in determining the mode and extent of effects of dietary (n-3) PUFA, especially on VLDL- and LDL-cholesterol levels. When dietary cholesterol intake was above 0.1% (w/w), the plasma cholesterol-lowering effect of (n-3) PUFA disappeared, and instead, it showed a cholesterol-increasing effect. However, the effects of dietary (n-3) PUFA on HDL-cholesterol are independent of dietary cholesterol content.
本研究旨在探讨膳食(n-3)多不饱和脂肪酸(PUFA)与不同膳食胆固醇含量之间的相互作用对仓鼠血浆和肝脏胆固醇的影响。雄性叙利亚仓鼠食用含膳食胆固醇含量逐步增加(0、0.025、0.05、0.1和0.2%,w/w)的饲料,饲料脂肪来源为(n-3)PUFA(21 g/100 g脂肪酸)或(n-6)PUFA(37.4 g/100 g脂肪酸),持续6周。在喂食非致动脉粥样硬化饮食(0或0.025%膳食胆固醇)的仓鼠中,(n-3)PUFA组的极低密度脂蛋白(VLDL)-胆固醇水平与(n-6)PUFA组无显著差异,且(n-3)PUFA组的低密度脂蛋白(LDL)-胆固醇水平显著低于(n-6)PUFA组。相反,在喂食致动脉粥样硬化饮食(0.1或0.2%膳食胆固醇)的仓鼠中,(n-3)PUFA组的VLDL-和LDL-胆固醇水平以剂量依赖方式显著高于(n-6)PUFA组。当仓鼠喂食0、0.025、0.05、0.1或0.2%(w/w)膳食胆固醇时,(n-3)PUFA组的高密度脂蛋白(HDL)胆固醇浓度显著低于(n-6)PUFA组。喂食致动脉粥样硬化饮食(0.1或0.2%膳食胆固醇)的(n-3)PUFA仓鼠的肝脏胆固醇酯显著较低,而肝脏微粒体酰基辅酶A:胆固醇酰基转移酶活性和VLDL-胆固醇酯显著高于喂食致动脉粥样硬化饮食的(n-6)PUFA仓鼠。我们的结果表明,膳食胆固醇的量是决定膳食(n-3)PUFA作用方式和程度的重要因素,尤其是对VLDL-和LDL-胆固醇水平。当膳食胆固醇摄入量高于0.1%(w/w)时,(n-3)PUFA的血浆胆固醇降低作用消失,反而表现出胆固醇升高作用。然而,膳食(n-3)PUFA对HDL-胆固醇的影响与膳食胆固醇含量无关。