| Literature DB >> 26381177 |
Yoshinori Osaki1, Yoshimi Nakagawa2, Shoko Miyahara3, Hitoshi Iwasaki3, Akiko Ishii4, Takashi Matsuzaka3, Kazuto Kobayashi3, Shigeru Yatoh3, Akimitsu Takahashi3, Naoya Yahagi3, Hiroaki Suzuki3, Hirohito Sone5, Ken Ohashi6, Shun Ishibashi7, Nobuhiro Yamada3, Hitoshi Shimano8.
Abstract
HMG-CoA reductase (HMGCR) catalyzes the conversion of HMG-CoA to mevalonic acid (MVA); this is the rate-limiting enzyme of the mevalonate pathway that synthesizes cholesterol. Statins, HMGCR inhibitors, are widely used as cholesterol-reducing drugs. However, statin-induced myopathy is the most adverse side effect of statins. To eludicate the mechanisms underlying statin the myotoxicity and HMGCR function in the skeletal muscle, we developed the skeletal muscle-specific HMGCR knockout mice. Knockout mice exhibited postnatal myopathy with elevated serum creatine kinase levels and necrosis. Myopathy in knockout mice was completely rescued by the oral administration of MVA. These results suggest that skeletal muscle toxicity caused by statins is dependent on the deficiencies of HMGCR enzyme activity and downstream metabolites of the mevalonate pathway in skeletal muscles rather than the liver or other organs.Entities:
Keywords: HMG-CoA reductase; Knockout mice; Mevalonic acid; Necrosis; Rhabdomyolysis; Skeletal muscle
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Year: 2015 PMID: 26381177 DOI: 10.1016/j.bbrc.2015.09.065
Source DB: PubMed Journal: Biochem Biophys Res Commun ISSN: 0006-291X Impact factor: 3.575