Vitamin D supplementation rescues simvastatin induced myopathy in mice via improving mitochondrial cristae shape

Statin induced myopathy (SIM) is a main deleterious effect leading to the poor treatment compliance, while the preventive or therapeutic treatments are absent. Mounting evidences demonstrated that vitamin D plays a vital role in muscle as a direct modulator. The deficiency of vitamin D was considere...

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Veröffentlicht in:Toxicology and applied pharmacology 2020-08, Vol.401, p.115076, Article 115076
Hauptverfasser: Ren, Lulu, Xuan, Lingling, Han, Feifei, Zhang, Jie, Gong, Lili, Lv, Yali, Zhang, Wen, Yang, Song, Xu, Benshan, Yan, Yan, Guo, Lifang, Liu, He, Wan, Zirui, Liu, Lihong
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Sprache:eng
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Zusammenfassung:Statin induced myopathy (SIM) is a main deleterious effect leading to the poor treatment compliance, while the preventive or therapeutic treatments are absent. Mounting evidences demonstrated that vitamin D plays a vital role in muscle as a direct modulator. The deficiency of vitamin D was considered as a cause of muscle dysfunction, whereas the supplementation resulted in a remission. However, there is no causal proof that vitamin D supplementation rescues SIM. Here, using the mice model of simvastatin-induced myopathy, we investigated the role of vitamin D supplementation and the mechanisms associated with mitochondria. Results indicated that simvastatin administration (80 mg/kg) impaired skeletal muscle with the increased serum creatine kinase (CK) level and the declined grip strength, which were alleviated by vitamin D supplementation. Moreover, vitamin D supplementation rescued the energy metabolism dysfunction in simvastatin-treated mice gastrocnemius by reducing the abnormal aggregation of muscular glycogen and lactic acid. Mitochondrial homeostasis plays a key role in the process of energy metabolism. Thus, the mitochondrial dysfunction is a mortal damage for the highly energy-requiring tissue. In our study, the mitochondrial cristae observed under transmission electron microscope (TEM) were lytic in simvastatin-treated gastrocnemius. Interestingly, vitamin D supplementation improved the mitochondrial cristae shape by regulating the expression of mitofusin-1/2 (MFN1/2), optic atrophy 1 (OPA1) and dynamin-related protein 1 (Drp1). As expected, the mitochondrial dysfunction and oxidative stress was mitigated by vitamin D supplementation. In conclusion, these findings suggested that moderate vitamin D supplementation rescued simvastatin induced myopathy via improving the mitochondrial cristae shape and function. •Vitamin D supplementation rescued simvastatin induced myopathy in mice.•Vitamin D supplementation improved the mitochondrial cristae shape.•Vitamin D supplementation mitigated mitochondrial dysfunction and oxidative stress in simvastatin-treated gastrocnemius.
ISSN:0041-008X
1096-0333
DOI:10.1016/j.taap.2020.115076