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首页> 外文期刊>The Journal of Experimental Biology >Multi-level regulation and metabolic scaling
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Multi-level regulation and metabolic scaling

机译:多级调节和代谢缩放

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Metabolic control analysis has revealed that flux through pathways is the consequence of system properties, i.e. shared control by multiple steps, as well as the kinetic effects of various pathways and processes over each other. This implies that the allometric scaling of flux rates must be understood in terms of properties that pertain to the regulation of flux rates. In contrast, proponents of models considering the scaling of branching or fractal-like systems suggest that supply rates determine metabolic rates. Therefore, the allometric scaling of supply alone provides a sufficient explanation for the allometric scaling of metabolism. Examination of empirical data from the literature of comparative physiology reveals that basal metabolic rates (BMR) are driven by rates of energy expenditure within internal organs and that the allometric scaling of BMR can be understood in terms of the scaling of the masses and metabolic rates of internal organs. Organ metabolic rates represent the sum of tissue metabolic rates while, within tissues, cellular metabolic rates are the outcome of shared regulation by multiple processes. Maximal metabolic rates (MMR, measured as maximum rates of O2 consumption, VO2max) during exercise also scale allometrically, are also subject to control by multiple processes, but are due mainly to O2 consumption by locomotory muscles. Thus, analyses of the scaling of MMR must consider the scaling of both muscle mass and muscle energy expenditure. Consistent with the principle of symmorphosis, allometry in capacities for supply (the outcome of physical design constraints) is observed to be roughly matched by allometry in capacities for demand (i.e. for energy expenditure). However, physiological rates most often fall far below maximum capacities and are subject to multi-step regulation. Thus, mechanistic explanations for the scaling of BMR and MMR must consider the manner in which capacities are matched and how rates are regulated at multiple levels of biological organization.
机译:代谢控制分析表明,通过途径的通量是系统特性的结果,即通过多个步骤进行共享控制,以及各种途径和过程相互之间的动力学效应。这意味着必须根据与通量率调节有关的特性来理解通量率的异度缩放。相反,考虑分支或分形系统规模缩放的模型的支持者建议,供给速率决定代谢速率。因此,仅供应的异形缩放就为代谢的异形缩放提供了充分的解释。对比较生理学文献中的经验数据进行检查后发现,基础代谢率(BMR)由内部器官内的能量消耗率驱动,并且BMR的异速结垢可以根据肿块的结垢和代谢率来理解。内部器官。器官代谢率代表组织代谢率的总和,而在组织内部,细胞代谢率是多个过程共同调节的结果。运动过程中的最大代谢率(MMR,以最大的O2消耗率,VO2max来衡量)也呈等比例关系,也受多个过程控制,但主要是由于运动肌肉消耗O2。因此,MMR缩放的分析必须考虑肌肉质量和肌肉能量消耗的缩放。与同构原理相一致,观察到供给能力的异向变化(物理设计约束的结果)与需求能力(即能量消耗)的异向变化大致匹配。但是,生理速率最常远低于最大容量,并且需要进行多步调节。因此,对BMR和MMR缩放的机械解释必须考虑容量匹配的方式以及如何在多个生物组织水平上调节速率。

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