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Modular control analysis of effects of chronic hypoxia on mouse heart

机译:慢性缺氧对小鼠心脏的模块化控制分析

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Modular control analysis of effects of chronic hypoxia on mouse heart. AmJPhysiol Regul Integr Comp Physiol 295: R1891-R1897,2008. First published October 1, 2008; doi:10.1152/ajpregu.90548.2008.-Modular control analysis (MoCA; Diolez P, Deschodt-Arsac V, Raffard G, Simon C, Santos PD, Thiaudiere E, Arsac L, Franconi JM. Am J Physiol Regul Integr Comp Physiol 293: R13-R19, 2007) was applied here on perfused hearts to describe the modifications of the regulation of heart energetics induced in mice exposed to 3-wk chronic hypoxia. MoCA combines 31P-NMR spectroscopy and modular (top down) control analysis to describe the integrative regulation of energy metabolism in the intact beating heart, on the basis of two modules [ATP/phosphocreatine (PCr) production and ATP/PCr consumption] connected by the energetic intermediates. In contrast with previous results in rat heart, in which all control of contraction was on ATP demand, mouse heart energetics presented a shared control of contraction between ATP/PCr-producing and -consuming modules. In chronic hypoxic mice, the decrease in heart contractile activity and PCr-to-ATP ratio was surprisingly associated with an important and significant higher response of ATP/PCr production (elasticity) to PCr changes compared with control hearts (-10.4 vs. -2.46). By contrast, no changes were observed in ATP/PCr consumption since comparable elasticities were observed. Since elasticities determine the regulation of energetics of heart contraction, the present results show that this new parameter may be used to uncover the origin of the observed dysfunctions under chronic hypoxia conditions. Considering the decrease in mitochondrial content reported after exposure to chronic hypoxia, it appears that the improvement of ATP/PCr production response to ATP demand may be viewed as a positive adaptative mechanism. It now appears crucial to understand the very processes responsible for ATP/PCr producer elasticity toward the energetic intermediates, as well as their regulation#
机译:慢性缺氧对小鼠心脏影响的模块化控制分析。 AmJPhysiol Regul Integr Comp Physiol 295:R1891-R1897,2008。首次发布于2008年10月1日; doi:10.1152 / ajpregu.90548.2008.-模块化控制分析(MoCA; Diolez P,Deschodt-Arsac V,Raffard G,Simon C,Santos PD,Thiaudiere E,Arsac L,Franconi JM.Am J Physiol Regul Integr Comp Physiol 293: R13-R19,2007)在这里应用于灌注心脏,以描述在暴露于3周慢性缺氧的小鼠中诱导的心脏能量调节的修改。 MoCA基于两个模块[ATP /磷酸肌酸(PCr)的产生和ATP / PCr的消耗],将31P-NMR光谱学和模块化(自上而下)控制分析相结合,以描述完整搏动心脏中能量代谢的整体调节。充满活力的中间体。与先前大鼠心脏的所有控制收缩均取决于ATP需求的结果相反,小鼠心脏能量学在ATP / PCr产生和消耗模块之间呈现出共同的收缩控制。在慢性低氧小鼠中,与对照组相比,心脏收缩活性和PCr / ATP比值的降低令人惊讶地与ATP / PCr产生(弹性)对PCr变化的重要且显着更高的响应相关(-10.4与-2.46 )。相反,由于观察到相当的弹性,因此未观察到ATP / PCr消耗量的变化。由于弹性决定了心脏收缩能量的调节,因此本研究结果表明,该新参数可用于揭示慢性低氧条件下观察到的功能障碍的起因。考虑到慢性缺氧暴露后线粒体含量减少,看来对ATP需求的ATP / PCr产生反应的改善可能被视为一种积极的适应性机制。现在看来,了解导致ATP / PCr生产者对高能中间体产生弹性的过程及其调控至关重要。

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