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Toxicol Appl Pharmacol ; 485: 116900, 2024 Apr.
Article in English | MEDLINE | ID: mdl-38508403

ABSTRACT

One of the major hitches for statins' utilization is the development of myotoxicity. Versatile studies reported that the underlining molecular mechanisms including coenzyme Q10 (CoQ10)/ubiquinone depletion, as well as the disturbance in the cytoplasmic Ca2+ homeostasis. Therefore, we investigated the consequences of supplementing CoQ10 and dantrolene, a cytoplasmic Ca2+ reducing agent, in combination with simvastatin. This adjuvant therapy normalized the simvastatin-mediated elevation in serum ALT, AST, CK-MM, as well as tissue Ca2+ content, in addition to suppressing the simvastatin-mediated oxidative stress in simvastatin-treated rats, while having no effect upon statin-induced antihyperlipidemic effect. Additionally, the combination inhibited the simvastatin-induced TGF-ß/ Smad4 pathway activation. Collectively, the current study emphasizes on the potential utilization of dantrolene and CoQ10 as an adjuvant therapy to statins treatment for improving their side effect profile.


Subject(s)
Dantrolene , Diet, High-Fat , Hydroxymethylglutaryl-CoA Reductase Inhibitors , Reactive Oxygen Species , Signal Transduction , Simvastatin , Smad4 Protein , Transforming Growth Factor beta , Ubiquinone , Ubiquinone/analogs & derivatives , Animals , Dantrolene/pharmacology , Dantrolene/therapeutic use , Ubiquinone/pharmacology , Hydroxymethylglutaryl-CoA Reductase Inhibitors/pharmacology , Signal Transduction/drug effects , Male , Reactive Oxygen Species/metabolism , Simvastatin/pharmacology , Smad4 Protein/metabolism , Rats , Transforming Growth Factor beta/metabolism , Diet, High-Fat/adverse effects , Muscular Diseases/chemically induced , Muscular Diseases/metabolism , Muscular Diseases/prevention & control , Drug Therapy, Combination , Oxidative Stress/drug effects , Rats, Wistar
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