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Regulation of Cardiac Energetics: Role of Redox State and Cellular Compartmentation during Ischemia

机译:心脏能量的调节:氧化还原状态和细胞分区在缺血过程中的作用

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The heart is capable of altering its metabolic rate during exercise or ischemia. Under most state transitions, the heart maintains the concentration of adenosine triphosphate (ATP) at relatively constant values, in spite of large fluctuations in metabolic rate or in the delivery of fuels and oxygen. However, the mechanisms responsible for the regulation of cardiac energetics under conditions of increased demand or reduced supply are still under debate. To improve quantitative understanding of the regulation of glycolysis and oxidative phosphorylation under physiological and pathological conditions, it is essential to assess the dynamics of cytosolic and mitochondrial nicotinamide adenine dinucleotide (NAD~+) and its reduced form (NADH) during stress (e.g., ischemia, exercise). However, at present there are no reliable methods to measure the dynamics of redox state in vivo in these subcellular compartments. In the present study, computer simulations with a mathematical model of myocardial energy metabolism are used to investigate the role of cytosolic and mitochondrial redox states in regulating cardiac energetics during reduced myocardial blood flow.
机译:心脏能够在运动或缺血期间改变其代谢率。在大多数状态过渡下,心脏在相对恒定的值下保持腺苷三磷酸(ATP)的浓度,尽管代谢速率或燃料和氧​​气递送大幅波动。但是,负责在需求增加或减少供应情况下调节心脏能量的机制仍在辩论下。为了提高对生理和病理条件下糖酵解和氧化磷酸化调节的定量理解,必须在应激期间评估细胞溶质和线粒体烟酰胺腺嘌呤二核苷酸腺嘌呤(NAD〜+)的动态(例如,缺血, 锻炼)。然而,目前没有可靠的方法来测量这些亚细胞室内体内氧化还原状态的动态。在本研究中,使用心肌能量代谢的数学模型的计算机模拟用于探讨细胞溶质和线粒体氧化还原态在减少心肌血流期间的心脏能量中的作用。

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