کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
5562251 1562608 2017 7 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Rosuvastatin safety: An experimental study of myotoxic effects and mitochondrial alterations in rats
موضوعات مرتبط
علوم زیستی و بیوفناوری علوم محیط زیست بهداشت، سم شناسی و جهش زایی
پیش نمایش صفحه اول مقاله
Rosuvastatin safety: An experimental study of myotoxic effects and mitochondrial alterations in rats
چکیده انگلیسی


- Atorvastatin and rosuvastatin induced myotoxic symptoms in rats.
- Rosuvastatin had slight myotoxic manifestations compared to atorvastatin.
- Effect of atorvastatin on mitochondrial functions was more evident than rosuvastatin.

Myopathy is the most commonly reported adverse effect of statins. All statins are associated with myopathy, though with different rates. Rosuvastatin is a potent statin reported to induce myopathy comparable to earlier statins. However, in clinical practice most patients could tolerate rosuvastatin over other statins. This study aimed to evaluate the myopathic pattern of rosuvastatin in rats using biochemical, functional and histopathological examinations. The possible deleterious effects of rosuvastatin on muscle mitochondria were also examined. The obtained results were compared to myopathy induced by atorvastatin in equimolar dose. Results showed that rosuvastatin induced a rise in CK, a slight increase in myoglobin level together with mild muscle necrosis. Motor activity, assessed by rotarod, showed that rosuvastatin decreased rats' performance. All these manifestations were obviously mild compared to the prominent effects of atorvastatin. Parallel results were obtained in mitochondrial dysfunction parameters. Rosuvastatin only induced a slight increase in LDH and a minor decrease in ATP (∼14%) and pAkt (∼12%). On the other hand, atorvastatin induced an increase in LDH, lactate/pyruvate ratio and a pronounced decline in ATP (∼80%) and pAkt (∼65%). These findings showed that rosuvastatin was associated with mild myotoxic effects in rats, especially when compared to atorvastatin.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Toxicology Letters - Volume 265, 4 January 2017, Pages 23-29
نویسندگان
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