Statins Trigger Mitochondrial Reactive Oxygen Species-Induced Apoptosis in Glycolytic Skeletal Muscle

Although statins are the most widely used cholesterol-lowering agents, they are associated with a variety of muscle complaints. The goal of this study was to characterize the effects of statins on the mitochondrial apoptosis pathway induced by mitochondrial oxidative stress in skeletal muscle using...

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Vydané v:	Antioxidants & redox signaling Ročník 24; číslo 2; s. 84
Hlavní autori:	Bouitbir, Jamal, Singh, François, Charles, Anne-Laure, Schlagowski, Anna-Isabel, Bonifacio, Annalisa, Echaniz-Laguna, Andoni, Geny, Bernard, Krähenbühl, Stephan, Zoll, Joffrey
Médium:	Journal Article
Jazyk:	English
Vydavateľské údaje:	United States 10.01.2016
Predmet:	Animals Apoptosis - drug effects Deltoid Muscle - cytology Deltoid Muscle - drug effects Deltoid Muscle - metabolism Glycolysis - drug effects Hydrogen Peroxide - metabolism Hydroxymethylglutaryl-CoA Reductase Inhibitors - adverse effects Hydroxymethylglutaryl-CoA Reductase Inhibitors - pharmacology Male Mitochondria - drug effects Mitochondria - metabolism Muscle, Skeletal - cytology Muscle, Skeletal - drug effects Muscle, Skeletal - metabolism Muscular Diseases - chemically induced Muscular Diseases - metabolism Oxidative Stress - drug effects Rats Rats, Wistar Reactive Oxygen Species - metabolism Signal Transduction - drug effects
ISSN:	1557-7716, 1557-7716
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Shrnutí:	Although statins are the most widely used cholesterol-lowering agents, they are associated with a variety of muscle complaints. The goal of this study was to characterize the effects of statins on the mitochondrial apoptosis pathway induced by mitochondrial oxidative stress in skeletal muscle using human muscle biopsies as well as in vivo and in vitro models. Statins increased mitochondrial H2O2 production, the Bax/Bcl-2 ratio, and TUNEL staining in deltoid biopsies of patients with statin-associated myopathy. Furthermore, atorvastatin treatment for 2 weeks at 10 mg/kg/day in rats increased H2O2 accumulation and mRNA levels and immunostaining of the Bax/Bcl-2 ratio, as well as TUNEL staining and caspase 3 cleavage in glycolytic (plantaris) skeletal muscle, but not in oxidative (soleus) skeletal muscle, which has a high antioxidative capacity. Atorvastatin also decreased the GSH/GSSG ratio, but only in glycolytic skeletal muscle. Cotreatment with the antioxidant, quercetin, at 25 mg/kg/day abolished these effects in plantaris. An in vitro study with L6 myoblasts directly demonstrated the link between mitochondrial oxidative stress following atorvastatin exposure and activation of the mitochondrial apoptosis signaling pathway. Treatment with atorvastatin is associated with mitochondrial oxidative stress, which activates apoptosis and contributes to myopathy. Glycolytic muscles are more sensitive to atorvastatin than oxidative muscles, which may be due to the higher antioxidative capacity in oxidative muscles. There is a link between statin-induced mitochondrial oxidative stress and activation of the mitochondrial apoptosis signaling pathway in glycolytic skeletal muscle, which may be associated with statin-associated myopathy.
Bibliografia:	ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23
ISSN:	1557-7716 1557-7716
DOI:	10.1089/ars.2014.6190