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Alteration of mitochondrial function in a model of chronic ischemia in vivo in rat heart.

机译:大鼠心脏体内慢性缺血模型中线粒体功能的改变。

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摘要

The aim of this study was to investigate mitochondrial alterations in an animal model of chronic myocardial ischemia in rats obtained by surgical constriction of the left coronary artery. Resting coronary blood flow was measured using the fluorescent microsphere technique. Contractile function, defined by rate-pressure product, and myocardial oxygen consumption were measured in a Langendorff preparation. The mitochondrial function was evaluated on permeabilized skinned fibers. Three weeks after surgery, ischemic hearts showed a significant decrease in coronary blood flow compared with sham. Hemodynamic measurements showed a significant systolic and diastolic dysfunction. Alterations in mitochondrial function in ischemic hearts were mainly characterized by a significant decrease in the maximal velocity and apparent half-saturation constant for ADP, loss of the stimulatory effect of creatine, and a stimulatory effect of exogenous cytochrome c. These functional alterations were supported by structural alterations characterized by mitochondrial clustering and swelling associated with membrane rupture. We conclude that the alterations in systolic function after chronic ischemia are supported by severe modifications of mitochondrial structure and function.
机译:这项研究的目的是调查通过左冠状动脉的手术收缩获得的大鼠的慢性心肌缺血的动物模型中的线粒体改变。使用荧光微球技术测量静止的冠状动脉血流量。在Langendorff制剂中测量收缩率功能(由速率压力乘积定义)和心肌耗氧量。在透化的皮肤纤维上评估线粒体功能。手术后三周,与假手术相比,缺血性心脏的冠状动脉血流明显减少。血液动力学测量显示明显的收缩和舒张功能障碍。缺血性心脏线粒体功能的改变主要表现为ADP的最大速度和表观半饱和常数显着降低,肌酸的刺激作用丧失以及外源性细胞色素c的刺激作用。这些功能性改变以线粒体聚集和与膜破裂相关的肿胀为特征的结构性改变得到支持。我们得出的结论是,慢性缺血后收缩功能的改变得到了线粒体结构和功能的严重修饰。

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