C57Bl/6 N mice on a western diet display reduced intestinal and hepatic cholesterol levels despite a plasma hypercholesterolemia

被引:47
作者
Desmarchelier, Charles [1 ]
Dahlhoff, Christoph [1 ,2 ]
Keller, Sylvia [3 ]
Sailer, Manuela [1 ]
Jahreis, Gerhard [3 ]
Daniel, Hannelore [1 ]
机构
[1] Tech Univ Munich, Mol Nutr Unit, D-85350 Freising Weihenstephan, Germany
[2] Tech Univ Munich, ZIEL Res Ctr Nutr & Food Sci, PhD Grad Sch Epigenet Imprinting & Nutr, D-85350 Freising Weihenstephan, Germany
[3] Univ Jena, Inst Nutr, D-07743 Jena, Germany
关键词
CHAIN FATTY-ACIDS; 3-BETA-HYDROXYSTEROL DELTA(14)-REDUCTASE; LIPID-METABOLISM; GENE-EXPRESSION; ABSORPTION; TRANSPORT; OBESITY; TARGET; PHOSPHATIDYLCHOLINE; IDENTIFICATION;
D O I
10.1186/1471-2164-13-84
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 [微生物学]; 090105 [作物生产系统与生态工程];
摘要
Background: Small intestine and liver greatly contribute to whole body lipid, cholesterol and phospholipid metabolism but to which extent cholesterol and phospholipid handling in these tissues is affected by high fat Western-style obesogenic diets remains to be determined. Methods: We therefore measured cholesterol and phospholipid concentration in intestine and liver and quantified fecal neutral sterol and bile acid excretion in C57Bl/6 N mice fed for 12 weeks either a cholesterol-free high carbohydrate control diet or a high fat Western diet containing 0.03% (w/w) cholesterol. To identify the underlying mechanisms of dietary adaptations in intestine and liver, changes in gene expression were assessed by microarray and qPCR profiling, respectively. Results: Mice on Western diet showed increased plasma cholesterol levels, associated with the higher dietary cholesterol supply, yet, significantly reduced cholesterol levels were found in intestine and liver. Transcript profiling revealed evidence that expression of numerous genes involved in cholesterol synthesis and uptake via LDL, but also in phospholipid metabolism, underwent compensatory regulations in both tissues. Alterations in glycerophospholipid metabolism were confirmed at the metabolite level by phospolipid profiling via mass spectrometry. Conclusions: Our findings suggest that intestine and liver react to a high dietary fat intake by an activation of de novo cholesterol synthesis and other cholesterol-saving mechanisms, as well as with major changes in phospholipid metabolism, to accommodate to the fat load.
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页数:16
相关论文
共 64 条
[1]
Intestinal lipoprotein overproduction in insulin-resistant states [J].
Adeli, Khosrow ;
Lewis, Gary F. .
CURRENT OPINION IN LIPIDOLOGY, 2008, 19 (03) :221-228
[2]
Niemann-Pick C1 like 1 protein is critical for intestinal cholesterol absorption [J].
Altmann, SW ;
Davis, HR ;
Zhu, LJ ;
Yao, XR ;
Hoos, LM ;
Tetzloff, G ;
Iyer, SPN ;
Maguire, M ;
Golovko, A ;
Zeng, M ;
Wang, LQ ;
Murgolo, N ;
Graziano, MP .
SCIENCE, 2004, 303 (5661) :1201-1204
[3]
Hypertriglyceridemia as a cardiovascular risk factor [J].
Austin, MA ;
Hokanson, JE ;
Edwards, KL .
AMERICAN JOURNAL OF CARDIOLOGY, 1998, 81 (4A) :7B-12B
[4]
Disruption of the gene encoding 3β-hydroxysterol Δ14-reductase (Tm7sf2) in mice does not impair cholesterol biosynthesis [J].
Bennati, Anna M. ;
Schiavoni, Gianluca ;
Franken, Sebastian ;
Piobbico, Danilo ;
Della Fazia, Maria A. ;
Caruso, Donatella ;
De Fabiani, Emma ;
Benedetti, Laura ;
De Angelis, Maria G. Cusella ;
Gieselmann, Volkmar ;
Servillo, Giuseppe ;
Beccari, Tommaso ;
Roberti, Rita .
FEBS JOURNAL, 2008, 275 (20) :5034-5047
[5]
Sterol dependent regulation of human TM7SF2 gene expression:: Role of the encoded 3β-hydroxysterol Δ14-reductase in human cholesterol biosynthesis [J].
Bennati, Anna Maria ;
Castelli, Marilena ;
Della Fazia, Maria Agnese ;
Beccari, Tommaso ;
Caruso, Donatella ;
Servillo, Giuseppe ;
Roberti, Rita .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS, 2006, 1761 (07) :677-685
[6]
Phospholipid scramblase: An update [J].
Bevers, Edouard M. ;
Williamson, Patrick L. .
FEBS LETTERS, 2010, 584 (13) :2724-2730
[7]
Dietary fat intake does affect obesity! [J].
Bray, GA ;
Popkin, BM .
AMERICAN JOURNAL OF CLINICAL NUTRITION, 1998, 68 (06) :1157-1173
[8]
NSDHL, an enzyme involved in cholesterol biosynthesis, traffics through the Golgi and accumulates on ER membranes and on the surface of lipid droplets [J].
Caldas, H ;
Herman, GE .
HUMAN MOLECULAR GENETICS, 2003, 12 (22) :2981-2991
[9]
Cartwright IJ, 1999, J LIPID RES, V40, P1858
[10]
Identification of a Physiologically Relevant Endogenous Ligand for PPARα in Liver [J].
Chakravarthy, Manu V. ;
Lodhi, Irfan J. ;
Yin, Li ;
Malapaka, Raghu R. V. ;
Xu, H. Eric ;
Turk, John ;
Semenkovich, Clay F. .
CELL, 2009, 138 (03) :476-488