Traumatic brain injury (TBI) continues to be a serious societal problem affecting at least 1.4 million Americans each year. Despite the significance of this public health problem and long term efforts of brain trauma research, the precise mechanisms and tolerances of brain injury have not yet been fully established. Currently, animal TBI experimental models are extensively used to study neurological responses which could not be investigated with cadavers. However, the intracranial mechanical responses, which have been hypothesized to govern brain injuries, are hard to observe directly, especially in vivo.
The ultimate goal of this study is to further investigate brain injury mechanism and tolerance at tissue level. To achieve this goal, first, a 3-D anatomically detailed high resolution finite element (FE) model of the rat brain was developed and validated against in vivo measured brain displacement data induced by dynamic cortical impact.
The FE rat brain model was then used to investigate rat brain contusion mechanism and associated FE model-specific injury threshold in the controlled cortical impact (CCI) model. The intracranial pressure was found to be uncorrelated with contusion induced by CCI. A threshold of 26.5% maximum principal strain (MPS) correlates with experimentally measured contusion volume at 24 hours post injury while a higher MPS threshold (30%) was required to predict contusion volume measured at 7- to 14-day post-injury.
The regional intracranial MPS’s predicted by the FE model were found to correlate well with in vivo observed percentage of cell loss as a result of CCI. Therefore, a new measure entitled cumulative strain damage percentage measurement (CSDPM), which accounts for the strain magnitude, the corresponding percentage of cell loss, and the volume ratio, is proposed.
The intracranial responses in an experimental model designed to induce axonal injury characterized as neurofilament compaction (NFC) was computationally analyzed. Results showed that a peak MPS of above 0.121 or compressive strain of above 0.222 correlate with NFC injury. However, the shear strain and intracranial pressure did not correlate with of NFC injury.
Finally, systematic analyses based on computational design of experiments for CCI were performed. The effect of external impact parameters on internal responses, including the contusion volume and CSDPM score, were described. The numerical rat brain model could be used to computationally design more refined experimental models of neurotrauma in the future