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3-羟基-3-甲基戊二酰辅酶A还原酶抑制剂对缺血犬心脏线粒体呼吸的影响。

Effects of 3-hydroxy-3-methylglutaryl coenzyme A reductase inhibitors on mitochondrial respiration in ischaemic dog hearts.

作者信息

Satoh K, Yamato A, Nakai T, Hoshi K, Ichihara K

机构信息

Department of Pharmacology, Hokkaido College of Pharmacy, Otaru, Japan.

出版信息

Br J Pharmacol. 1995 Sep;116(2):1894-8. doi: 10.1111/j.1476-5381.1995.tb16679.x.

Abstract
  1. Effects of 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase inhibitors, pravastatin and simvastatin, on the myocardial level of coenzyme Q10, and on mitochondrial respiration were examined in dogs. 2. Either vehicle (control), pravastatin (4 mg kg-1 day-1), or simvastatin (2 mg kg-1 day-1) was administered orally for 3 weeks. First, the myocardial tissue level of coenzyme Q10 was determined in the 3 groups. Second, ischaemia was induced by ligating the left anterior descending coronary artery (LAD) in anaesthetized open chest dogs, pretreated with the inhibitors. After 30 min of ischaemia, nonischaemic and ischaemic myocardium were removed from the left circumflex and LAD regions, respectively, and immediately used for isolation of mitochondria. The mitochondrial respiration was determined by polarography, with glutamate and succinate used as substrates. 3. Simvastatin significantly decreased the myocardial level of coenzyme Q10, but pravastatin did not. 4. Ischaemia decreased the mitochondrial respiratory control index (RCI) in both groups. Significant differences in RCI between nonischaemic and ischaemic myocardium were observed in the control and simvastatin-treated groups. 5. Only in the simvastatin-treated group did ischaemia significantly decrease the ADP/O ratio, determined with succinate. 6. The present results indicate that simvastatin but not pravastatin may cause worsening of the myocardial mitochondrial respiration during ischaemia, probably because of reduction of the myocardial coenzyme Q10 level.
摘要
  1. 在犬类中研究了3-羟基-3-甲基戊二酰辅酶A(HMG-CoA)还原酶抑制剂普伐他汀和辛伐他汀对心肌辅酶Q10水平及线粒体呼吸的影响。2. 分别口服给予溶媒(对照组)、普伐他汀(4毫克/千克/天)或辛伐他汀(2毫克/千克/天),持续3周。首先,测定三组动物心肌组织中辅酶Q10的水平。其次,对经抑制剂预处理的麻醉开胸犬,通过结扎左冠状动脉前降支(LAD)诱导缺血。缺血30分钟后,分别从左旋支和LAD区域取出非缺血和缺血心肌,立即用于分离线粒体。以谷氨酸和琥珀酸为底物,通过极谱法测定线粒体呼吸。3. 辛伐他汀显著降低了心肌辅酶Q10水平,但普伐他汀没有。4. 缺血降低了两组的线粒体呼吸控制指数(RCI)。在对照组和辛伐他汀治疗组中,非缺血和缺血心肌的RCI存在显著差异。5. 仅在辛伐他汀治疗组中,缺血显著降低了以琥珀酸为底物测定的ADP/O比值。6. 目前的结果表明,辛伐他汀而非普伐他汀可能会导致缺血期间心肌线粒体呼吸恶化,这可能是由于心肌辅酶Q10水平降低所致。

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