Abstract

It was analyzed in normal physiological arteries whether the least energy principle would suffice to account for the radius exponent x. The mammalian arterial system was modeled as two types, the elastic or the rigid, to which Bernoulli's and Hagen‐Poiseuille's equations were applied, respectively. We minimized the total energy function E, which was defined as the sum of kinetic, pressure, metabolic and thermal energies, and loss of each per unit time in a single artery transporting viscous incompressible blood. Assuming a scaling exponent α between the vessel radius (r) and length (l) to be 1.0, x resulted in 2.33 in the elastic model. The rigid model provided a continuously changing x from 2.33 to 3.0, which corresponded to Uylings’ and Murray's theories, respectively, through a function combining Reynolds number with a proportional coefficient of the l − r relationship. These results were expanded to an asymmetric arterial fractal tree with the blood flow preservation rule. While x in the optimal elastic model accounted for around 2.3 in proximal systemic (r >1 mm) and whole pulmonary arteries (r ≥0.004 mm), optimal x in the rigid model explained 2.7 in elastic‐muscular (0.1 < r ≤1 mm) and 3.0 in peripheral resistive systemic arteries (0.004 ≤ r ≤0.1 mm), in agreement with data obtained from angiographic, cast‐morphometric, and in vivo experimental studies in the literature. The least energy principle on the total energy basis provides an alternate concept of optimality relating to mammalian arterial fractal dimensions under α = 1.0.

Highlights

  • Mean aortic blood pressure falls only 2% from the ascending aorta to small arteries whose inner radius (r) narrows to ~1 mm (Struijker-Boudier 2009) in the human systemic circulation (Nichols et al 2011)

  • Hagen-Poiseuille’s equation has long been used universally to express the pressure gradient in arterial models including Murray’s theory, irrespective of whether r is derived from big arteries like aorta or from small peripheral arterioles (Murray 1926; Suwa and Takahashi 1971; Uylings 1977; Sherman 1981; Mayrovitz and Roy 1983; Rossitti and Lo€fgren 1993; Kassab and Fung 1995; LaBarbera 1995; West et al 1997; Dawson et al 1999; Gafiychuk and Lubashevsky 2001; Kizilova 2006; Ghorishi et al 2007; Kamiya and Takahashi 2007; Nakamura et al 2011)

  • X was directly derived from equations

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Summary

Introduction

Mean aortic blood pressure falls only 2% from the ascending aorta to small arteries whose inner radius (r) narrows to ~1 mm (Struijker-Boudier 2009) (or ~2.5 mm, Nichols et al 2011) in the human systemic circulation (Nichols et al 2011). Hagen-Poiseuille’s equation has long been used universally to express the pressure gradient in arterial models including Murray’s theory, irrespective of whether r is derived from big arteries like aorta or from small peripheral arterioles (Murray 1926; Suwa and Takahashi 1971; Uylings 1977; Sherman 1981; Mayrovitz and Roy 1983; Rossitti and Lo€fgren 1993; Kassab and Fung 1995; LaBarbera 1995; West et al 1997; Dawson et al 1999; Gafiychuk and Lubashevsky 2001; Kizilova 2006; Ghorishi et al 2007; Kamiya and Takahashi 2007; Nakamura et al 2011). Theoretical results were compared with either reported and/or our own estimated results and discussed in relation to conventional theories

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