Enriched environment (EE) has no effect on acute brain injury after
ICH. (a) Experimental design. The timeline shows the sequence of
all behavioral tests and experimental procedures, beginning on
the day of surgery (day 0). LFB: Luxol fast blue; CV: Cresyl
violet; BWC: Brain water content; OFT: open field test; EPM:
elevated plus-maze; MWM: Morris Water Maze; NOR: novel object
recognition; FST: forced swim test; TST: tail suspension test;
SPT: sucrose preference test; LDT: light/dark transition test;
WB: western blot; IF: immunofluorescence; HPLC: high-performance
liquid chromatography; GA: glutaminase activity. (b) On day 3
after ICH, mice exposed to EE did not reduce brain water content
in the ipsilateral hemisphere compared to mice that received ICH
and standard conditions (ICH + SE). n = 5 mice/group.
p > 0.05 vs. the sham group (one-way
ANOVA followed by Bonferroni’s post hoc test). Cont-Stri,
contralateral striatum; Ipsi-Stri, ipsilateral striatum;
Cerebel, cerebellum. (c) Top: Representative Luxol fast
blue/crystal violet-stained brain sections of the ICH + SE and
ICH + EE groups (scale bar = 1 mm). Bottom: High magnifications
of the dashed areas in the top photograph on the ipsilateral and
contralateral side (Scale bar= 50 μm) (d) The plot graph shows
EE did not increase the percentage of areas with normal myelin
after ICH on day 3. n = 3 mice/group (t-test).
(e) Quantification analysis did not show differences in brain
injury volume between the ICH + SE and ICH + EE groups. n = 8
mice/group (t-test). (f) Left: Schematic
illustration of the spatial extent of the hemorrhagic lesion
72 h after microinjection of collagenase VII into the left
striatum. Right: Representative fresh brain sections show
hematomas (red areas) in mice exposed to standard conditions or
EE and (g) Quantification analysis did not show differences in
hematoma volume between the ICH + SE and ICH + EE groups. n = 6
mice/group (t-test). Data are
expressed as mean ± SD.