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首页> 外文期刊>The Journal of Physiology >Phosphate metabolite concentrations and ATP hydrolysis potential in normal and ischaemic hearts.
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Phosphate metabolite concentrations and ATP hydrolysis potential in normal and ischaemic hearts.

机译:正常和缺血性心脏中的磷酸盐代谢物浓度和ATP水解潜力。

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To understand how cardiac ATP and CrP remain stable with changes in work rate - a phenomenon that has eluded mechanistic explanation for decades - data from (31)phosphate-magnetic resonance spectroscopy ((31)P-MRS) are analysed to estimate cytoplasmic and mitochondrial phosphate metabolite concentrations in the normal state, during high cardiac workstates, during acute ischaemia and reactive hyperaemic recovery. Analysis is based on simulating distributed heterogeneous oxygen transport in the myocardium integrated with a detailed model of cardiac energy metabolism. The model predicts that baseline myocardial free inorganic phosphate (P(i)) concentration in the canine myocyte cytoplasm - a variable not accessible to direct non-invasive measurement - is approximately 0.29 mm and increases to 2.3 mm near maximal cardiac oxygen consumption. During acute ischaemia (from ligation of the left anterior descending artery) P(i) increases to approximately 3.1 mm and ATP consumption in the ischaemic tissue is reduced quickly to less than half its baseline value before the creatine phosphate (CrP) pool is 18% depleted. It is determined from these experiments that the maximal rate of oxygen consumption of the heart is an emergent property and is limited not simply by the maximal rate of ATP synthesis, but by the maximal rate at which ATP can be synthesized at a potential at which it can be utilized. The critical free energy of ATP hydrolysis for cardiac contraction that is consistent with these findings is approximately -63.5 kJ mol(-1). Based on theoretical findings, we hypothesize that inorganic phosphate is both the primary feedback signal for stimulating oxidative phosphorylation in vivo and also the most significant product of ATP hydrolysis in limiting the capacity of the heart to hydrolyse ATP in vivo. Due to the lack of precise quantification of P(i) in vivo, these hypotheses and associated model predictions remain to be carefully tested experimentally.
机译:若要了解心脏ATP和CrP如何随着工作率的变化而保持稳定-数十年来一直无法解释这种现象-对(31)磷酸核磁共振光谱((31)P-MRS)的数据进行了分析以估计细胞质和线粒体在正常状态下,高心脏工作状态下,急性缺血和反应性高血氧恢复期间,磷酸盐代谢物浓度较高。分析是基于模拟心肌中分布的异质氧转运,并结合了心脏能量代谢的详细模型。该模型预测,犬心肌细胞质中的基线心肌游离无机磷酸盐(P(i))浓度-不能直接进行非侵入式测量的变量-约为0.29 mm,并在最大心脏耗氧量附近增加至2.3 mm。在急性缺血(从左前降支结扎)中,P(i)增加至大约3.1 mm,缺血组织中的ATP消耗迅速减少至其基线值的一半以下,而磷酸肌酸(CrP)池为18%耗尽。从这些实验中可以确定,心脏的最大耗氧量是一种紧急状态,不仅受ATP合成的最大速率限制,还受ATP在其潜在电位下合成的最大速率的限制。可以利用。 ATP水解的心脏收缩的临界自由能与这些发现一致,约为-63.5 kJ mol(-1)。基于理论发现,我们假设无机磷酸盐既是体内刺激氧化磷酸化的主要反馈信号,也是限制心脏在体内水解ATP的能力的ATP水解的最重要产物。由于缺乏体内P(i)的精确定量,这些假设和相关的模型预测仍有待通过实验进行仔细测试。

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