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载脂蛋白E表型对胆固醇代谢调节的影响。

Impact of apo E phenotype on the regulation of cholesterol metabolism.

作者信息

Miettinen T A

机构信息

Second Department of Medicine, University of Helsinki, Finland.

出版信息

Ann Med. 1991 Apr;23(2):181-6. doi: 10.3109/07853899109148045.

Abstract

Cholesterol absorption was positively related to the apo E subscript in middle aged men on their normal home diet. The apo E subscript (e.g. E2/2 = 1, E2/3 = 2, E2/4 = 3...) was negatively associated with cholesterol synthesis and fractional removal of LDL apo B and positively with the total and LDL cholesterol and LDL apo B concentrations. Cholesterol elimination, especially as bile acids, was most effective in subjects with epsilon 2 allele. A slight reduction of biliary deoxycholic acid content in the men with the epsilon 4 allele and a negative correlation between deoxycholic acid and cholesterol absorption suggested that intestinal bacterial function may contribute to the positive association of cholesterol absorption to the apo E phenotype. Reduction of fat and cholesterol consumption lowered while an increase of dietary cholesterol enhanced the LDL cholesterol concentration proportionately to the apo E subscript when cholesterol absorption efficiency was reduced in proportion to fat intake. Low absorption, effective elimination and high synthesis of cholesterol associated with low synthesis and effective removal of LDL apo B seem to be factors keeping serum cholesterol low during different diets. The findings also suggest that the apo E phenotypes regulate cholesterol metabolism during basal conditions and serum cholesterol responses to dietary modifications.

摘要

在正常家庭饮食的中年男性中,胆固醇吸收与载脂蛋白E亚型呈正相关。载脂蛋白E亚型(例如,E2/2 = 1,E2/3 = 2,E2/4 = 3……)与胆固醇合成以及低密度脂蛋白载脂蛋白B的分数清除呈负相关,与总胆固醇、低密度脂蛋白胆固醇和低密度脂蛋白载脂蛋白B浓度呈正相关。胆固醇清除,尤其是以胆汁酸形式的清除,在携带ε2等位基因的受试者中最为有效。携带ε4等位基因的男性胆汁中脱氧胆酸含量略有降低,且脱氧胆酸与胆固醇吸收之间呈负相关,这表明肠道细菌功能可能有助于胆固醇吸收与载脂蛋白E表型之间的正相关。当胆固醇吸收效率与脂肪摄入量成比例降低时,减少脂肪和胆固醇摄入会降低低密度脂蛋白胆固醇浓度,而增加膳食胆固醇则会按载脂蛋白E亚型比例相应提高低密度脂蛋白胆固醇浓度。低胆固醇吸收、有效清除以及高胆固醇合成与低密度脂蛋白载脂蛋白B的低合成和有效清除相关,这些似乎是不同饮食期间维持血清胆固醇水平较低的因素。研究结果还表明,载脂蛋白E表型在基础状态下调节胆固醇代谢以及血清胆固醇对饮食变化的反应。

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