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Fibrates and statins rapidly and synergistically induce pyruvate dehydrogenase kinase 4 mRNA in the liver and muscles of mice.

机译:贝特类药物和他汀类药物在小鼠肝脏和肌肉中快速协同地诱导丙酮酸脱氢酶激酶4 mRNA。

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摘要

We previously identified pyruvate dehydrogenase kinase 4 (PDK4) mRNA as a most rapidly induced mRNA by fibrates and suggested the possibility that the coupled induction of PDK4 and reduction of serum triglyceride and fatty acid levels can cause protein degradation in muscles. To investigate whether the drugs that are known to have a risk of rhabdomyolysis induce PDK4 mRNA in skeletal muscle, the effects of statins and new quinolon anti-bacterial drugs on the expression levels of the mRNA were examined using mice and cultured cells. Several statins and new quinolon anti-bacterial drugs solely induced PDK4 mRNA in the muscle as efficiently as fibrates and at least some combinations were synergistic. The present results suggest that induction of PDK4 mRNA is involved in the drug induced acute rhabdomyolysis when the muscle is restricted to use fatty acids as a major energy source.
机译:我们先前确定丙酮酸脱氢酶激酶4(PDK4)mRNA是贝特类药物诱导最快的mRNA,并提出了PDK4的耦合诱导以及血清甘油三酸酯和脂肪酸水平降低会导致肌肉蛋白质降解的可能性。为了研究已知有横纹肌溶解风险的药物是否会在骨骼肌中诱导PDK4 mRNA,使用小鼠和培养细胞检查了他汀类药物和新型喹诺酮类抗菌药物对mRNA表达水平的影响。几种他汀类药物和新的喹诺酮类抗菌药物仅能像贝特类药物一样有效地诱导肌肉中的PDK4 mRNA,并且至少某些组合具有协同作用。目前的结果表明,当肌肉被限制使用脂肪酸作为主要能量来源时,PDK4 mRNA的诱导与药物诱导的急性横纹肌溶解有关。

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