Dh. Smith et al., CHARACTERIZATION OF DIFFUSE AXONAL PATHOLOGY AND SELECTIVE HIPPOCAMPAL DAMAGE FOLLOWING INERTIAL BRAIN TRAUMA IN THE PIG, Journal of neuropathology and experimental neurology, 56(7), 1997, pp. 822-834
Dynamic deformation applied to white matter tracts is a common feature
of human brain trauma, and may result in diffuse axonal injury (DAI).
To produce DAI in an experimental model, we have utilized nonimpact i
nertial loading to induce brain trauma in miniature swine. This specie
s was chosen due to its large gyrencephalic brain with substantial whi
te matter domains. Twenty anesthetized (2% isoflurane) miniature swine
were subjected to pure impulsive centroidal rotation 110 degrees in t
he coronal plane in 4 to 6 ms; peak accelerations ranged from 0.6 to 1
.7 x 10(5) rad/s(2). Seven days following injury, the brains were fixe
d (4% paraformaldehyde). Histopathologic examination was performed on
40 mu m sections stained with cresyl violet (Nissl), antibodies target
ing neurofilament (axonal damage). GFAP (astrocytes), and pig IgG (pro
tein extravasation). Widespread multifocal axonal injury was observed
in combination with gliosis throughout the brain, most commonly in the
root of gyri and at the interface of the gray and white matter. Very
little vascular disruption was noted in regions of axonal injury. Neur
onal damage was primarily found in the CA1 and CA3 subfields of the hi
ppocampus. These results suggest that this model is clinically relevan
t and useful for evaluating mechanisms of inertial brain trauma.