Source:http://linkedlifedata.com/resource/pubmed/id/18820241
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
2009-1-16
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pubmed:abstractText |
Multiple studies suggest increased conversion of cholesterol to bile acids by cholesterol 7alpha-hydroxylase (CYP7A1) protects against dyslipidemia and atherosclerosis. CYP7A1 expression is repressed by the sequential activity of two nuclear hormone receptors, farnesoid X receptor (FXR) and small heterodimer partner (SHP). Here we demonstrate 129 strain SHP(-/-) mice are protected against hypercholesterolemia resulting from either a cholesterol/cholic acid (chol/CA) diet or from hypothyroidism. In a mixed 129-C57Bl/6 background, LDLR(-/-) and LDLR(-/-)SHP(-/-) mice had nearly identical elevations in hepatic cholesterol content and repression of cholesterol regulated genes when fed a Western diet. However, the LDLR(-/-)SHP(-/-) mice had greatly reduced elevations in serum VLDL and LDL cholesterol levels and triglyceride (TG) levels as compared with LDLR(-/-) mice. Additionally, the hepatic inflammation produced by the Western diet in the LDLR(-/-) mice was abolished in the LDLR(-/-)SHP(-/-) mice. CYP7A1 expression was induced 10-fold by the Western diet in the LDLR(-/-)SHP(-/-) mice but not in the LDLR(-/-) mice. Finally, hepatocyte-specific deletion of SHP expression was also protective against dyslipidemia induced by either a chol/CA diet or by hypothyroidism. While no antagonist ligands have yet been identified for SHP, these results suggest selective inhibition of hepatic SHP expression may provide protection against dyslipidemia.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Cholesterol, LDL,
http://linkedlifedata.com/resource/pubmed/chemical/Cholesterol, VLDL,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Cytoplasmic and Nuclear,
http://linkedlifedata.com/resource/pubmed/chemical/nuclear receptor subfamily 0...
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pubmed:status |
MEDLINE
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pubmed:month |
Feb
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pubmed:issn |
0022-2275
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
50
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
193-203
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pubmed:meshHeading |
pubmed-meshheading:18820241-Animals,
pubmed-meshheading:18820241-Cholesterol, LDL,
pubmed-meshheading:18820241-Cholesterol, VLDL,
pubmed-meshheading:18820241-Dyslipidemias,
pubmed-meshheading:18820241-Gene Expression,
pubmed-meshheading:18820241-Liver,
pubmed-meshheading:18820241-Mice,
pubmed-meshheading:18820241-Mice, Transgenic,
pubmed-meshheading:18820241-Receptors, Cytoplasmic and Nuclear
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pubmed:year |
2009
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pubmed:articleTitle |
Loss of small heterodimer partner expression in the liver protects against dyslipidemia.
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pubmed:affiliation |
Cardiovascular and Metabolic Disease Research, Wyeth Research, Collegeville, PA 19426, USA.
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pubmed:publicationType |
Journal Article
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