Sustained deficits in behavioral function and white matter atrophy
persist up to 6 months postinjury. (a) Mice with rmCHI spent more time
in open arms of the elevated plus maze at both 1 (one-way ANOVA),
F(2, 25) = 18.31, p < .0001,
and 6 MPI (one-way ANOVA), F(2, 19) = 9.960,
p = .0011. (b) Mice with rmCHI were more active in
the elevated plus maze at 6 MPI, but not at 1 MPI (6 MPI; one-way
ANOVA), F(2, 19) = 10.26, p = .0010.
(c) At 6 MPI, but not at 2 MPI, rmCHI mice spent less time not moving in
the forced swim test compared with both 0- and 1-hit groups (one-way
ANOVA), F(2, 19) = 15.62,
p < .0001. (d) At both 2 MPI and 6 MPI, mice with
rmCHI spent more time classified as “high mobility”: 2 MPI, one-way
ANOVA, F(2, 25) = 3.542, p < .0442;
6 MPI, one-way ANOVA, F(2, 17) = 15.21,
p = .0002. (e) Mice with 10 hits were unable to
learn the location of the hidden platform in the Morris water maze at 6
MPI (two-way ANOVA), F(8, 76) = 2.858,
p < .0078. (f) Mice with 10 hits had significant
white matter atrophy compared with both sham and 1-hit mice (one-way
ANOVA), F(2, 15) = 2.532, p < .01,
and (g) corpus callosum volume measured at 6 MPI negatively correlated
with latency to time in open arms during the elevated plus maze at 2 MPI
(r= −.78, p = .0001). (h) Corpus
callosum volume also negatively correlated with MWM Day 5 latency to
find the platform at 6 MPI (r= −.674,
p = .0011).
rmCHI = repeated mild closed head injury; MPI = months postinjury;
ANOVA = analysis of variance; MWM = Morris water maze.