Mechanism of Resistance to Dietary Cholesterol

被引:21
作者
Boone, Lindsey R. [1 ,2 ]
Brooks, Patricia A. [2 ]
Niesen, Melissa I. [2 ]
Ness, Gene C. [2 ]
机构
[1] Univ Pittsburgh, McGowan Inst Regenerat Med, Dept Pathol, Pittsburgh, PA 15219 USA
[2] Univ S Florida, Coll Med, Dept Mol Med, Tampa, FL 33612 USA
关键词
D O I
10.1155/2011/101242
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Background. Alterations in expression of hepatic genes that could contribute to resistance to dietary cholesterol were investigated in Sprague-Dawley rats, which are known to be resistant to the serum cholesterol raising action of dietary cholesterol. Methods. Microarray analysis was used to provide a comprehensive analysis of changes in hepatic gene expression in rats in response to dietary cholesterol. Changes were confirmed by RT-PCR analysis. Western blotting was employed to measure changes in hepatic cholesterol 7 alpha hydroxylase protein. Results. Of the 28,000 genes examined using the Affymetrix rat microarray, relatively few were significantly altered. As expected, decreases were observed for several genes that encode enzymes of the cholesterol biosynthetic pathway. The largest decreases were seen for squalene epoxidase and lanosterol 14 alpha demethylase (CYP 51A1). These changes were confirmed by quantitative RT-PCR. LDL receptor expression was not altered by dietary cholesterol. Critically, the expression of cholesterol 7 alpha hydroxylase, which catalyzes the rate-limiting step in bile acid synthesis, was increased over 4-fold in livers of rats fed diets containing 1% cholesterol. In contrast, mice, which are not resistant to dietary cholesterol, exhibited lower hepatic cholesterol 7 alpha hydroxylase (CYP7A1) protein levels, which were not increased in response to diets containing 2% cholesterol.
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页数:9
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