Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
2571851 | Toxicology and Applied Pharmacology | 2007 | 7 Pages |
Abstract
Lowering of low-density lipoprotein cholesterol is well achieved by 3-hydroxy-3-methylglutaryl-coenzyme A (HMG-CoA) reductase inhibitors (statins). Statins inhibit the conversion of HMG-CoA to mevalonate, a precursor for cholesterol and coenzyme Q10 (CoQ10). In HepG2 cells, simvastatin decreased mitochondrial CoQ10 levels, and at higher concentrations was associated with a moderately higher degree of cell death, increased DNA oxidative damage and a reduction in ATP synthesis. Supplementation of CoQ10, reduced cell death and DNA oxidative stress, and increased ATP synthesis. It is suggested that CoQ10 deficiency plays an important role in statin-induced hepatopathy, and that CoQ10 supplementation protects HepG2 cells from this complication.
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Authors
S. Tavintharan, C.N. Ong, K. Jeyaseelan, M. Sivakumar, S.C. Lim, C.F. Sum,