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植物甾醇和甾烷醇:对混合微胶粒组成及肝X受体(靶基因)激活的影响。

Plant sterols and stanols: effects on mixed micellar composition and LXR (target gene) activation.

作者信息

Plat Jogchum, Nichols Jason A, Mensink Ronald P

机构信息

Department of Human Biology, Maastricht University, 6200 MD Maastricht, The Netherlands.

出版信息

J Lipid Res. 2005 Nov;46(11):2468-76. doi: 10.1194/jlr.M500272-JLR200. Epub 2005 Sep 8.

Abstract

Plant stanols and sterols of the 4-desmethyl family (e.g., sitostanol and sitosterol) effectively decrease LDL cholesterol concentrations, whereas 4,4-dimethylsterols (alpha-amyrin and lupeol) do not. Serum carotenoid concentrations, however, are decreased by both plant sterol families. The exact mechanisms underlying these effects are not known, although effects on micellar composition have been suggested. With a liver X receptor (LXR) coactivator peptide recruitment assay, we showed that plant sterols and stanols from the 4-desmethylsterol family activated both LXRalpha and LXRbeta, whereas 4,4-dimethyl plant sterols did not. In fully differentiated Caco-2 cells, the functionality of this effect was shown by the increased expression of ABCA1, one of the known LXR target genes expressed by Caco-2 cells in measurable amounts. The LXR-activating potential of the various plant sterols/stanols correlated positively with ABCA1 mRNA expression. Reductions in serum hydrocarbon carotenoids could be explained by the effects of the 4-desmethyl family and 4,4-dimethylsterols on micellar carotenoid incorporation. Our findings indicate that the decreased intestinal absorption of cholesterol and carotenoids by plant sterols and stanols is caused by two distinct mechanisms.

摘要

4-去甲基家族的植物甾烷醇和甾醇(如谷甾烷醇和谷甾醇)能有效降低低密度脂蛋白胆固醇浓度,而4,4-二甲基甾醇(α-香树脂醇和羽扇豆醇)则不能。然而,这两类植物甾醇都会降低血清类胡萝卜素浓度。尽管有人提出这些作用与胶束组成有关,但这些作用的确切机制尚不清楚。通过肝脏X受体(LXR)共激活因子肽募集试验,我们发现4-去甲基甾醇家族的植物甾醇和甾烷醇能激活LXRα和LXRβ,而4,4-二甲基植物甾醇则不能。在完全分化的Caco-2细胞中,ABCA1(Caco-2细胞中可检测表达的已知LXR靶基因之一)表达增加,表明了这种作用的功能性。各种植物甾醇/甾烷醇的LXR激活潜力与ABCA1 mRNA表达呈正相关。血清烃类类胡萝卜素的减少可以用4-去甲基家族和4,4-二甲基甾醇对胶束类胡萝卜素掺入的影响来解释。我们的研究结果表明,植物甾醇和甾烷醇降低胆固醇和类胡萝卜素的肠道吸收是由两种不同的机制引起的。

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