Xu Zuyuan, Le Khuong, Moghadasian Mohammed H
Department of Human Nutritional Sciences, University of Manitoba, Winnipeg, Canada R2H 2A6; Canadian Center for Agri-food Research in Health and Medicine, St. Boniface Hospital Research Center, Winnipeg, Canada R2H 2A6.
J Nutr Biochem. 2008 Aug;19(8):545-554. doi: 10.1016/j.jnutbio.2007.06.012. Epub 2007 Dec 21.
Dietary phytosterols significantly reduce plasma cholesterol concentrations and atherosclerosis in apolipoprotein E-knockout (apo E-KO) mice. We investigated the long-term effects of phytosterol treatment on gene expression in the liver of these mice. Male apo E-KO mice were fed an atherogenic diet supplemented with (n=6) or without (n=6) 2% (wt/wt) phytosterol mixtures for 14 weeks. Liver specimens were collected and stored in RNAlater immediately. mRNA was extracted and subjected to microarray analyses and real-time quantitative reverse transcription-polymerase chain reaction (RT-PCR) assay for confirmation. Oligonuleotide microarray analysis of pooled samples (n=3) revealed that the expression of 132 genes/transcripts was significantly altered in treated animals, considering the false discovery rate (FDR) of 0.23. Real-time RT-PCR techniques confirmed these alterations in the expression of several of these genes, including Hmgcr (2.16-fold; P=.0002), Hmgcs1 (1.79-fold; P=.001), Hsd17b7 (2.11-fold; P=.028), Sqle (2.03-fold; P=.01), Cyp51 (1.8-fold; P=.001), Fads1 (1.55-fold; P=.031), Fads2 (2.17-fold; P=.047), Lpin1 (3.67-fold; P=.001), Ppargc1b (PGC-1beta; a coactivator of sterol-regulatory element-binding proteins; 1.66-fold; P=.007) and Cyp7B1 (1.81-fold; P=.025). In summary, our data suggest that long-term dietary phytosterols can alter the expression of a number of hepatic genes that regulate sterol metabolism in apo E-KO mice. It is possible that these changes are due to inhibition of cholesterol absorption, but are not a direct effect of plant sterols. Further multivariate correlation or association analysis is needed to establish the relations between changes in the expression of these genes and prevention of atherosclerosis by phytosterols.
膳食植物甾醇可显著降低载脂蛋白E基因敲除(apo E-KO)小鼠的血浆胆固醇浓度并减轻动脉粥样硬化。我们研究了植物甾醇处理对这些小鼠肝脏基因表达的长期影响。给雄性apo E-KO小鼠喂食添加(n = 6)或不添加(n = 6)2%(重量/重量)植物甾醇混合物的致动脉粥样化饮食14周。立即收集肝脏标本并保存在RNA Later中。提取mRNA并进行微阵列分析以及实时定量逆转录-聚合酶链反应(RT-PCR)检测以进行确认。对合并样本(n = 3)的寡核苷酸微阵列分析显示,考虑到错误发现率(FDR)为0.23,处理组动物中有132个基因/转录本的表达发生了显著改变。实时RT-PCR技术证实了其中几个基因表达的这些变化,包括Hmgcr(2.16倍;P = 0.0002)、Hmgcs1(1.79倍;P = 0.001)、Hsd17b7(2.11倍;P = 0.028)、Sqle(2.03倍;P = 0.01)、Cyp51(1.8倍;P = 0.001)、Fads1(1.55倍;P = 0.031)、Fads2(2.17倍;P = 0.047)、Lpin1(3.67倍;P = 0.001)、Ppargc1b(PGC-1β;固醇调节元件结合蛋白的共激活因子;1.66倍;P = 0.007)和Cyp7B1(1.81倍;P = 0.025)。总之,我们的数据表明,长期膳食植物甾醇可改变apo E-KO小鼠中许多调节甾醇代谢的肝脏基因的表达。这些变化可能是由于胆固醇吸收受到抑制,但并非植物甾醇的直接作用。需要进一步进行多变量相关性或关联性分析,以确定这些基因表达变化与植物甾醇预防动脉粥样硬化之间的关系。