Allometric Scaling by the Length of the Circulatory Network

A. Szász
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引用次数: 2

Abstract

Background: Allometric scaling is a well-known research tool used for the metabolic rates of organisms. It measures the living systems with fractal physiology. The metabolic rate versus the mass of the living species has a definite scaling and behaves like a four-dimensional phenomenon. The extended investigations focus on the mass-dependence of the various physiological parameters. Objective: Proving the length of vascularization is the scaling parameter instead of mass in allometric relation. Method: The description of the energy balance of the ontogenic growth of the tumor is an extended cell-death parameter for studying the mass balance at the cellular level. Results: It is shown that when a malignant cellular cluster tries to maximize its metabolic rate, it changes its allometric scaling exponent. A growth description could follow the heterogenic development of the tumor. The mass in the allometric scaling could be replaced by the average length of the circulatory system in each case. Conclusion: According to this concept, the dependence of the mass in allometric scaling is replaced with a more fundamental parameter, the length character of the circulatory system. The introduced scaling parameter has primary importance in cancer development, where the elongation of the circulatory length by angiogenesis is in significant demand.
循环网络长度的异速缩放
背景:异速标度是一种众所周知的用于生物体代谢率的研究工具。它用分形生理学来测量生命系统。代谢率与活物种质量的关系有一定的比例,表现得像一个四维现象。扩展的研究集中在各种生理参数的质量依赖性上。目的:证明血管长度是标度参数,而不是异速关系中的质量。方法:描述肿瘤个体生长的能量平衡是在细胞水平上研究质量平衡的一个扩展的细胞死亡参数。结果:当恶性细胞簇试图使其代谢率最大化时,它会改变其异速缩放指数。生长描述可以跟随肿瘤的异质性发展。在每种情况下,异速标度中的质量可以用循环系统的平均长度来代替。结论:根据这一概念,异速标度中质量的依赖性被一个更基本的参数所取代,即循环系统的长度特征。引入的标度参数在癌症发展中具有重要意义,其中血管生成对循环长度的延长是非常重要的。
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