Cell viability in intervertebral disc under various nutritional and dynamic loading conditions: 3d Finite element analysis

被引:86
作者
Zhu, Qiaoqiao [1 ]
Jackson, Alicia R. [2 ]
Gu, Wei Yong [1 ]
机构
[1] Univ Miami, Tissue Biomech Lab, Dept Mech & Aerosp Engn, Coll Engn, Coral Gables, FL 33124 USA
[2] Univ Miami, Orthopaed Biomech Lab, Dept Biomed Engn, Coral Gables, FL 33124 USA
关键词
Biomechanics; Mechanobiology; Transport phenomena; Nutrition; Glucose concentration; Cell density; Dynamic compression; Mixture theory; BIOLOGICAL SOFT-TISSUES; LOW-BACK-PAIN; NUCLEUS PULPOSUS; SOLUTE TRANSPORT; IN-VIVO; PHYSICAL SIGNALS; ANNULUS FIBROSUS; END-PLATE; UNCONFINED COMPRESSION; CONFINED COMPRESSION;
D O I
10.1016/j.jbiomech.2012.08.044
中图分类号
Q6 [生物物理学];
学科分类号
071011 [生物物理学];
摘要
In this study, a new cell density model was developed and incorporated into the formulation of the mechano-electrochemical mixture theory to investigate the effects of deprivation of nutrition supply at boundary source, degeneration, and dynamic loading on the cell viability of intervertebral disc (IVD) using finite element methods. The deprivation of nutrition supply at boundary source was simulated by reduction in nutrition level at CEP and AF boundaries. Cases with 100%, 75%, 60%, 50% and 30% of normal nutrition level at both CEP and AF boundaries were modeled. Unconfined axial sinusoidal dynamic compressions with different combinations of amplitude (u =10% +/- 2.5%, +/- 5%) and frequency (f=1, 10, 20 cycle/day) were applied. Degenerated IVD was modeled with altered material properties. Cell density decreased substantially with reduction of nutrition level at boundaries. Cell death was initiated primarily near the NP-AF interface on the mid-plane. Dynamic loading did not result in a change in the cell density in non-degenerated IVD, since glucose levels did not fall below the minimum value for cell survival; in degenerated IVDs, we found that increasing frequency and amplitude both resulted in higher cell density, because dynamic compression facilitates the diffusion of nutrients and thus increases the nutrition level around IVD cells. The novel computational model can be used to quantitatively predict both when and where cells start to die within the IVD under various kinds of nutritional and mechanical conditions. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2769 / 2777
页数:9
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