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哮喘气道壁多尺度模型中的静态和动态应力非均质性。

Static and dynamic stress heterogeneity in a multiscale model of the asthmatic airway wall.

作者信息

Hiorns J E, Jensen O E, Brook B S

机构信息

School of Mathematical Sciences, University of Nottingham, Nottingham, United Kingdom; and.

School of Mathematics, University of Manchester, Manchester, United Kingdom.

出版信息

J Appl Physiol (1985). 2016 Jul 1;121(1):233-47. doi: 10.1152/japplphysiol.00715.2015. Epub 2016 May 19.

Abstract

Airway hyperresponsiveness (AHR) is a key characteristic of asthma that remains poorly understood. Tidal breathing and deep inspiration ordinarily cause rapid relaxation of airway smooth muscle (ASM) (as demonstrated via application of length fluctuations to tissue strips) and are therefore implicated in modulation of AHR, but in some cases (such as application of transmural pressure oscillations to isolated intact airways) this mechanism fails. Here we use a multiscale biomechanical model for intact airways that incorporates strain stiffening due to collagen recruitment and dynamic force generation by ASM cells to show that the geometry of the airway, together with interplay between dynamic active and passive forces, gives rise to large stress and compliance heterogeneities across the airway wall that are absent in tissue strips. We show further that these stress heterogeneities result in auxotonic loading conditions that are currently not replicated in tissue-strip experiments; stresses in the strip are similar to hoop stress only at the outer airway wall and are under- or overestimates of stresses at the lumen. Taken together these results suggest that a previously underappreciated factor, stress heterogeneities within the airway wall and consequent ASM cellular response to this micromechanical environment, could contribute to AHR and should be explored further both theoretically and experimentally.

摘要

气道高反应性(AHR)是哮喘的一个关键特征,但目前仍了解甚少。潮气呼吸和深吸气通常会导致气道平滑肌(ASM)迅速舒张(通过对组织条施加长度波动来证明),因此与AHR的调节有关,但在某些情况下(如对离体完整气道施加跨壁压力振荡),这种机制会失效。在此,我们使用一个针对完整气道的多尺度生物力学模型,该模型纳入了由于胶原蛋白募集导致的应变强化以及ASM细胞产生的动态力,以表明气道的几何形状,以及动态主动力和被动力之间的相互作用,会导致气道壁上出现组织条中不存在的较大应力和顺应性异质性。我们进一步表明,这些应力异质性会导致目前在组织条实验中无法复制的辅助张力加载条件;组织条中的应力仅在外气道壁处与环向应力相似,并且低估或高估了管腔内的应力。综合这些结果表明,一个此前未被充分认识的因素,即气道壁内的应力异质性以及ASM细胞对这种微机械环境的相应反应,可能导致AHR,应在理论和实验上进一步探索。

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