Spinal cord injury and its devastating consequences are the subject of inte
nsive research aimed at reversing or at least minimizing functional loss, R
esearch efforts focus on either attenuating the post-injury spread of damag
e (secondary degeneration) or inducing some regeneration. In most of these
studies, as well as in clinical situations, evaluation of the state of the
injured spinal cord poses a serious difficulty. To address this problem, we
carried out a diffusion-weighted MRI experiment and developed an objective
routine for quantifying anisotropy in injured rat spinal cords. Rats were
subjected to a contusive injury of the spinal cord caused by a controlled w
eight drop. Untreated control rats were compared with rats treated with T c
ells specific to the central nervous system self-antigen myelin basic prote
in, a form of therapy recently shown to be neuroprotective, After the rats
were killed their excised spinal cords were fixed in formalin and imaged by
multislice spin echo MRI, using two orthogonal diffusion gradients. Appare
nt diffusion coefficient (ADC) values and anisotropy ratio (Al) maps were e
xtracted on a pixel-by-pixel basis. The calculated sum of Al values (SAl) f
or each slice was defined as a parameter representing the total amount of a
nisotropy. The mean-Al and SAI values increased gradually with the distance
from the site of the lesion. At the site itself, the mean-Al and SAI value
s were significantly higher in the spinal cords of the treated animals than
in the controls (P = 0.047, P = 0.028, respectively). These values were co
nsistent with the score of functional locomotion. The difference was also m
anifested in the Al maps, which revealed well-organized neural structure in
the treated rats but not in the controls. The SAI values, Al histograms, a
nd Al maps proved to be useful parameters for quantifying injury and recove
ry in an injured spinal cord. These results encourage the development of di
ffusion anisotropy MRI as a helpful approach for quantifying the extent of
secondary degeneration and measuring recovery after spinal cord injury. Mag
n Reson Med 45:1-9, 2001. (C) 2001 Wiley-Liss, Inc.