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. 2012 Jan 20;29(2):218–234. doi: 10.1089/neu.2011.1762

FIG. 5.

FIG. 5.

Lateral traumatic brain injury (TBI) generally caused transient increases in total cofilin immunoreactivity. Western blot analyses were repeated using an antibody recognizing cofilin regardless of serine 3 (Ser3) phosphorylation status (total cofilin). Analyses revealed time- and region-dependent changes in total cofilin immunoreactivity, relative to controls. In the ipsilateral hippocampus, for example, total cofilin immunoreactivity was increased at 1 h, 12 h, and 2 weeks post-TBI, relative to controls (A). In the contralateral hippocampus, total cofilin immunoreactivity also increased above control levels, but only weeks later, at 2 weeks post-TBI (B). Unlike all other brain regions tested, the ipsilateral neocortex showed a decrease in total cofilin immunoreactivity at 1 h post-TBI, relative to controls. However, total cofilin immunoreactivity returned to control levels by 12 h post-TBI, and then increased above control levels weeks later, at 2 weeks post-TBI (C). The contralateral neocortex underwent a delayed increase in total cofilin immunoreactivity at 24 h post-TBI, relative to controls (D). All comparisons were made by one-way analysis of variance with Dunnett's post-hoc test (*p<0.05, **p<0.01).