Source:http://linkedlifedata.com/resource/pubmed/id/20018177
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
8
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pubmed:dateCreated |
2010-2-17
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pubmed:abstractText |
The mechanism of statin-induced skeletal muscle myopathy is poorly understood. We investigated how simvastatin affects cholesterol metabolism, ubiquinone levels, and the prenylation and N-linked glycosylation of proteins in C2C12 myotubes. We used liver HepG2 cells for comparison, as their responses to statins are well-characterized in terms of their cholesterol metabolism (in contrast to muscle cells), and statins are well-tolerated in the liver. Differences between the two cell lines could indicate the mechanism behind statin-induced myopathy. Simvastatin reduced de novo cholesterol production in C2C12 myotubes by 95% after 18h treatment. The reduction was 82% in the HepG2 cells. Total cholesterol pools, however, remained constant in both cell lines. Simvastatin treatment similarly did not affect total ubiquinone levels in the myotubes, unlike in HepG2 cells (22% reduction in CoQ10). Statin treatment reduced levels of Ras and Rap1 prenylation in both cell lines, whereas N-linked glycosylation was only affected in C2C12 myotubes (21% reduction in rate). From these observations, we conclude that total cholesterol and ubiquinone levels are unlikely to be involved in statin-mediated myopathy, but reductions in protein prenylation and especially N-linked glycosylation may play a role. This first comparison of the responses to simvastatin between liver and skeletal muscle cell lines may be important for future research directions concerning statin-induced myopathy.
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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,
http://linkedlifedata.com/resource/pubmed/chemical/Hydroxymethylglutaryl-CoA...,
http://linkedlifedata.com/resource/pubmed/chemical/RNA, Messenger,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, LDL,
http://linkedlifedata.com/resource/pubmed/chemical/SREBF2 protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Simvastatin,
http://linkedlifedata.com/resource/pubmed/chemical/Sterol Regulatory Element Binding...,
http://linkedlifedata.com/resource/pubmed/chemical/Ubiquinone
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pubmed:status |
MEDLINE
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pubmed:month |
Apr
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pubmed:issn |
1873-2968
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pubmed:author | |
pubmed:copyrightInfo |
2009 Elsevier Inc. All rights reserved.
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pubmed:issnType |
Electronic
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pubmed:day |
15
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pubmed:volume |
79
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1200-9
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pubmed:meshHeading |
pubmed-meshheading:20018177-Cells, Cultured,
pubmed-meshheading:20018177-Cholesterol,
pubmed-meshheading:20018177-Glycosylation,
pubmed-meshheading:20018177-Hep G2 Cells,
pubmed-meshheading:20018177-Humans,
pubmed-meshheading:20018177-Hydroxymethylglutaryl-CoA Reductase Inhibitors,
pubmed-meshheading:20018177-Muscle Fibers, Skeletal,
pubmed-meshheading:20018177-Muscular Diseases,
pubmed-meshheading:20018177-Protein Prenylation,
pubmed-meshheading:20018177-RNA, Messenger,
pubmed-meshheading:20018177-Receptors, LDL,
pubmed-meshheading:20018177-Simvastatin,
pubmed-meshheading:20018177-Sterol Regulatory Element Binding Protein 2,
pubmed-meshheading:20018177-Ubiquinone
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pubmed:year |
2010
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pubmed:articleTitle |
Effect of simvastatin on cholesterol metabolism in C2C12 myotubes and HepG2 cells, and consequences for statin-induced myopathy.
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pubmed:affiliation |
Department of Research, University Hospital Basel, Switzerland. peter.mullen@unibas.ch
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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