The effect of sustained compression on oxygen metabolic transport in the intervertebral disc decreases with degenerative changes.

The effect of sustained compression on oxygen metabolic transport in the intervertebral disc decreases with degenerative changes.
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DOI:
10.1371/journal.pcbi.1002112
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发表时间:
2011-08
影响因子:
4.3
通讯作者:
Lacroix D
Lacroix D
中科院分区:
生物学2区
文献类型:
--
作者:
Malandrino A;Noailly J;Lacroix D

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Intervertebral disc metabolic transport is essential to the functional spine and provides the cells with the nutrients necessary to tissue maintenance. Disc degenerative changes alter the tissue mechanics, but interactions between mechanical loading and disc transport are still an open issue. A poromechanical finite element model of the human disc was coupled with oxygen and lactate transport models. Deformations and fluid flow were linked to transport predictions by including strain-dependent diffusion and advection. The two solute transport models were also coupled to account for cell metabolism. With this approach, the relevance of metabolic and mechano-transport couplings were assessed in the healthy disc under loading-recovery daily compression. Disc height, cell density and material degenerative changes were parametrically simulated to study their influence on the calculated solute concentrations. The effects of load frequency and amplitude were also studied in the healthy disc by considering short periods of cyclic compression. Results indicate that external loads influence the oxygen and lactate regional distributions within the disc when large volume changes modify diffusion distances and diffusivities, especially when healthy disc properties are simulated. Advection was negligible under both sustained and cyclic compression. Simulating degeneration, mechanical changes inhibited the mechanical effect on transport while disc height, fluid content, nucleus pressure and overall cell density reductions affected significantly transport predictions. For the healthy disc, nutrient concentration patterns depended mostly on the time of sustained compression and recovery. The relevant effect of cell density on the metabolic transport indicates the disturbance of cell number as a possible onset for disc degeneration via alteration of the metabolic balance. Results also suggest that healthy disc properties have a positive effect of loading on metabolic transport. Such relation, relevant to the maintenance of the tissue functional composition, would therefore link disc function with disc nutrition. Low back pain is a very common pathology in industrialized countries, often due to bad posture. It is also highly related to intervertebral disc aging. Aging of the disc is a normal process characterized by series of changes in its structure and function. The events that convert normal aging into degenerative disease is still not clear. Complications such as limited nutrition and possible reduction of disc cells with age make the issue intricate and multi-factorial. Using a numerical model that includes both nutritional and mechanical components, we found two different situations when looking at the effect of external loadings on two important cell solutes related with disc metabolism: oxygen and lactate. The effect of mechanical loading was greater when compressing a healthy disc than a degenerated one and promoted fluctuations of solutes concentrations. Also, changes in cell density seem fundamental in the process of disc degeneration and its causality with other degenerative changes should be further investigated. The importance of both mechanical and cellular patterns to maintain a healthy condition provides new insights to the field of disc regenerative medicine.
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