Ameliorative role of coenzyme Q10 against simvastatin induced myopathy of skeletal muscles in adult male albino rats.
Background: Simvastatin (SV) is one anti hyperlipidemic drugs. It acts by inhibition of HMG-CoA reductase. It can cause side effects, including muscle pain. Coenzyme Q10 (CoQ10) is present in the body as an antioxidant, as it is necessary for cell maintenance. Aim: This study was designated to evaluate the ability of CoQ10 to repair damaged skeletal muscle triggered by SV in albino rats. Material and Methods:40 adult male albino rats were used in this study, divided into 4 distinct groups; each was composed of 10 rats and received the drug diluted in distilled water via a gastric tube for a period of 12 weeks. Group I received a daily dosage of usual food and water. Group II administered SV at a dose of 10 mg/kg/day. Group III received SV at a dose of 10 mg/kg/day with CoQ10 at a dose of 10 mg/kg/day. Group IV received 10mg/kg/day of SV for 12 weeks, followed by 12weeks stopping of drug. At the end of experiment, muscle tissues of gastrocnemius were collected from groups and processed for H&E, PAS and toluidine blue. Biochemical analyses were conducted to assess levels of CK. Results: Administration of SV in group II leads to elevation in the CK with histological changes in muscle fiber in H&E, PAS and toluidine blue. On the other hand administration of CoQ10 in group III showed a significant decrease in CK, with improvement in architecture of the muscle fiber. Conclusion: CoQ10 administration improve the skeletal myopathy induced by SV.
Authors
- Shaimaa Fouad (ORCID: https://orcid.org/0000-0003-4052-9454)
- Hanan Ahmed Hussien Hussien
- Medhat Ata
- Fatma Alzahraa Fouad Abd Al-Baky
- Samah Abuzaid
- Elsyed Aly Mahran
Institutions
- Department of Embryology (US)
- Minia University (EG)
Publication Details
- Journal
- Minia Journal of Medical Research
- Published
- 2025-08-03
- DOI
- https://doi.org/10.21608/mjmr.2025.404125.2031
- Primary Topic
- Coenzyme Q10 studies and effects
- Type
- article
- Field-Weighted Citation Impact
- 0.00