Environmental enrichment enhances recovery of function but exacerbates ischemic cell death

被引:86
作者
Farrell, R [1 ]
Evans, S [1 ]
Corbett, D [1 ]
机构
[1] Mem Univ Newfoundland, Fac Med, St Johns, NF A1B 3V6, Canada
关键词
neuroplasticity; ischemic tolerance; rehabilitation; use-dependent injury;
D O I
10.1016/S0306-4522(01)00386-4
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Prior exposure to brief 'conditioning' episodes of ischemia protects hippocampal CAI neurons against a subsequent more severe ischemic insult. However, protected cells exhibit abnormal function and as survival times are extended this ischemic tolerance dissipates and cells begin to die. In this study, We Sought to determine Whether environmental enrichment could alter the above pattern of delayed cell death and functional impairment in a gerbil model of ischemic tolerance. Gerbils received either ischemic preconditioning, 5 min of ischemia without preconditioning or sham surgery. Three days after ischemia, gerbils were placed in either an enriched environment or standard laboratory housing. Open field habituation was assessed 3, 7. 10, 30 and 60 days after ischemia. Subsequently. animals were trained in two versions (win-shift and win-stay) of a T-maze task. Following behavioral testing, extracellular CAI field potential amplitudes and CAI cell counts were determined. Initial open field activity Was significantly higher in all experimental groups compared to sham animals (P < 0.001). By 60 days, enriched isciiernic preconditioned and enriched ischemic gerbils were not different than shams Whereas non-enriched. ischemic preconditioned and ischemic gerbils continued to have higher activity scores P <0.05). Preconditioned and enriched ischemic animals learned the win-shift T-maze problem as quickly as shams While non-enriched ischemic gerbils were severely impaired compared with all other groups (P < 0.001). Only the sham and enriched preconditioned groups readily acquired the win-stay paradigm. CAI field potential amplitudes were lower (P < 0.05) in ischemic than sham gerbils irrespective of treatment. Surprisingly, CAI cell counts Were significantly lower (P < 0.01) in enriched versus non-enriched ischemic preconditioned animals. These data demonstrate that early. intensive intervention after ischemia can improve functional outcome but that this is accompanied by increased brain damage, Careful consideration needs to be given to the timing of rehabilitation after stroke and related types of brain injury. (C) 2001 IBRO. Published by Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:585 / 592
页数:8
相关论文
共 55 条
[1]   Impairment of working memory in the T-maze after transient global cerebral ischemia in the Mongolian gerbil [J].
Andersen, MB ;
Sams-Dodd, F .
BEHAVIOURAL BRAIN RESEARCH, 1998, 91 (1-2) :15-22
[2]   DORSAL VENTRAL GRADIENT IN VULNERABILITY OF CA1 HIPPOCAMPUS TO ISCHEMIA - A COMBINED HISTOLOGICAL AND ELECTROPHYSIOLOGICAL STUDY [J].
ASHTON, D ;
VANREEMPTS, J ;
HASELDONCKX, M ;
WILLEMS, R .
BRAIN RESEARCH, 1989, 487 (02) :368-372
[3]  
AUER RN, 1989, J NEUROSCI, V9, P1641
[4]   LOCOMOTOR-ACTIVITY IN THE ISCHEMIC GERBIL [J].
BABCOCK, AM ;
BAKER, DA ;
LOVEC, R .
BRAIN RESEARCH, 1993, 625 (02) :351-354
[5]   Importance of preoperative training and maze difficulty in task performance following hippocampal damage in the gerbil [J].
Babcock, AM ;
GrahamGoodwin, H .
BRAIN RESEARCH BULLETIN, 1997, 42 (06) :415-419
[6]   Ischemic preconditioning and brain tolerance - Temporal histological and functional outcomes, protein synthesis requirement, and interleukin-1 receptor antagonist and early gene expression [J].
Barone, FC ;
White, RF ;
Spera, PA ;
Ellison, J ;
Currie, RW ;
Wang, XK ;
Feuerstein, GZ .
STROKE, 1998, 29 (09) :1937-1950
[7]  
BIERNASKIE J, 2001, IN PRESS J NEUROSCI
[8]   Early exclusive use of the affected forelimb after moderate transient focal ischemia in rats - Functional and anatomic outcome [J].
Bland, ST ;
Schallert, T ;
Strong, R ;
Aronowski, J ;
Grotta, JC .
STROKE, 2000, 31 (05) :1144-1151
[9]   Global ischemia and behavioural deficits [J].
Block, F .
PROGRESS IN NEUROBIOLOGY, 1999, 58 (03) :279-295