Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2013 Dec 9:1:19.
doi: 10.3389/fbioe.2013.00019. eCollection 2013.

Finite Element Modeling of CNS White Matter Kinematics: Use of a 3D RVE to Determine Material Properties

Affiliations

Finite Element Modeling of CNS White Matter Kinematics: Use of a 3D RVE to Determine Material Properties

Yi Pan et al. Front Bioeng Biotechnol. .

Abstract

Axonal injury represents a critical target area for the prevention and treatment of traumatic brain and spinal cord injuries. Finite element (FE) models of the head and/or brain are often used to predict brain injury caused by external mechanical loadings, such as explosive waves and direct impact. The accuracy of these numerical models depends on correctly determining the material properties and on the precise depiction of the tissues' microstructure (microscopic level). Moreover, since the axonal microstructure for specific regions of the brain white matter is locally oriented, the stress, and strain fields are highly anisotropic and axon orientation dependent. Additionally, mechanical strain has been identified as the proximal cause of axonal injury, which further demonstrates the importance of this multi-scale relationship. In this study, our previously developed FE and kinematic axonal models are coupled and applied to a pseudo 3-dimensional representative volume element of central nervous system white matter to investigate the multi-scale mechanical behavior. An inverse FE procedure was developed to identify material parameters of spinal cord white matter by combining the results of uniaxial testing with FE modeling. A satisfactory balance between simulation and experiment was achieved via optimization by minimizing the squared error between the simulated and experimental force-stretch curve. The combination of experimental testing and FE analysis provides a useful analysis tool for soft biological tissues in general, and specifically enables evaluations of the axonal response to tissue-level loading and subsequent predictions of axonal damage.

Keywords: axonal injury; microstructural properties; multi-scale modeling; spinal cord injury; traumatic brain injury.

PubMed Disclaimer

Figures

Figure 1
Figure 1
Finite element model of the undulated axons (A) and the extracellular matrix (B).
Figure 2
Figure 2
Numerical uniaxial tensile experiment at the stretch level of 1.06. (A) von Mises stress contour of the matrix of the RVE in which the undulated axons are embedded. (B) von Mises stress contour of the axons. Highly localized stress implies the effect of the axon geometry on local stress and strain field.
Figure 3
Figure 3
Flow chart of the optimization process.
Figure 4
Figure 4
Stress-stretch curves of E18 chick embryo spinal cord: the converged simulation vs. experimental in Shreiber et al. (2009).
Figure 5
Figure 5
Predicted evolution of undulation with stretch. Simulation results are compared to experimental results from Bain et al. (2003) and to simulation results from Karami et al. (2009) and Pan et al. (2011).
Figure 6
Figure 6
Plot of function value at various shear modulus. It shows that the squared error of the experimental curve and the simulated curve is minimized at μ = 36.63, 33.28, and 29.64 kPa for α = 6.95, 8.22, and 9.49, respectively.
Figure 7
Figure 7
Inverse simulation example: stress-stretch curves of chick embryo spinal cord with α = 8.22. The arrow points to the stress-stretch curve corresponding to the optimized parameter μ = 33.28 kPa.

References

    1. Assaf Y., Blumenfeld-Katzir T., Yovel Y., Basser P. J. (2008). AxCaliber: a method for measuring axon diameter distribution from diffusion MRI. Magn. Res. Medic. 59, 1347–135410.1002/mrm.21577 - DOI - PMC - PubMed
    1. Bain A. C., Billiar K. L., Shreiber D. I., McIntosh T. K., Meaney D. F. (1997). In vivo mechanical thresholds for traumatic axonal damage. Advisory Group for Aerospace Research and Development (AGARD) Meeting 199 (Mescalero, NM: ), 13 p.
    1. Bain A. C., Meaney D. F. (2000). Tissue-level thresholds for axonal damage in an experimental model of central nervous system white matter injury. J. Biomech. Eng. 122, 615–62210.1115/1.1324667 - DOI - PubMed
    1. Bain A. C., Shreiber D. I., Meaney D. F. (2003). Modeling of microstructural kinematics during simple elongation of central nervous system tissue. J. Biomech. Eng. 125, 798–80410.1115/1.1632627 - DOI - PubMed
    1. Cloots R. J. H., Gervaise H. M. T., van Dommelen J. A. W., Geers M. G. D. (2008). Biomechanics of traumatic brain injury: influences of the morphologic heterogeneities of the cerebral cortex. Ann. Biomed. Eng. 36, 1203–121510.1007/s10439-008-9510-3 - DOI - PMC - PubMed

LinkOut - more resources