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ARUP; ISBN: 978-0-9562121-5-3 - CMBBE 2012 - Cardiff University

ARUP; ISBN: 978-0-9562121-5-3 - CMBBE 2012 - Cardiff University

ARUP; ISBN: 978-0-9562121-5-3 - CMBBE 2012 - Cardiff University

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MECHANICAL EFFECT ON METABOLIC TRANSPORT AND CELL<br />

VIABILITY IN THE INTERVERTEBRAL DISC<br />

1. ABSTRACT<br />

A. Malandrino 1 , J. Noailly 2 and D. Lacroix 2,3<br />

The degeneration process in the intervertebral disc (IVD) is linked to progressive cell<br />

death and to mechanical factors. Therefore, the inclusion of cell viability criteria<br />

coupled with disc mechanics in a computational model would enable to get a better<br />

understanding of the degeneration process in IVD.<br />

A recently developed finite element (FE) model of the L4-L5 IVD based on<br />

poromechanics and IVD metabolism (Malandrino et al., 2011) was modified to include<br />

an exponential decay of cells over time below critical glucose and pH levels. The<br />

implementation was verified against in vitro literature data on cell viability. Viability<br />

criteria were used in the IVD model where diffusions of glucose, oxygen and lactate<br />

accounted for predicted porosity and volume changes. Subtissue-specific mechanical<br />

properties and cell concentrations were modelled. Daily compressive phases (standing<br />

and resting) were applied. Metabolite boundary concentrations were reduced at the<br />

endplates to induce critical conditions within the IVD. Solutions with and without<br />

mechanical coupling were compared.<br />

Critical glucose rather than pH levels were relevant to cell viability far away from the<br />

solute supply. Deformation couplings increased glucose in the disc centre so that cells<br />

stopped dying up to 10 hours earlier over two days simulated when mechanical<br />

deformations were considered. These results can help in the understanding of coupled<br />

mechanical and biological factors. If metabolite supply is disturbed, as it could happen<br />

during endplate calcification or circulatory diseases, a local accelerated cell death in the<br />

disc centre may occur in absence of tissue compliance. This study highlights the need to<br />

restore both nutritional and mechanical factors in order to favour cell viability along<br />

regenerative treatments.<br />

2. INTRODUCTION<br />

The study of cell death within the intervertebral disc (IVD) enables to understand better<br />

the process of disc degeneration. Recently, a model simulating the coupling between<br />

mechanical loading and the transport of metabolites has shown the effect of mechanics<br />

on transport (Malandrino et al., 2011). However, modelling the link between<br />

solute/metabolism concentrations and cell activity is still an open issue. In the literature<br />

1<br />

PhD candidate, Biomechanics and Mechanobiology Group, Institute for Bioengineering of Catalonia,<br />

Baldiri Reixac 4, 08028 Barcelona, Spain<br />

2<br />

Senior Researcher, Biomechanics and Mechanobiology Group, Institute for Bioengineering of Catalonia,<br />

Baldiri Reixac 4, 08028 Barcelona, Spain<br />

3<br />

Professor, Department of Mechanical Engineering, <strong>University</strong> of Sheffield, Mappin Street, Sheffield, S1<br />

3JD, UK

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