Age effect on motor recovery in a post-acute animal stroke model

被引:47
作者
Brown, AW [1 ]
Marlowe, KJ
Bjelke, B
机构
[1] Mayo Clin, Dept Phys Med & Rehabil, Rochester, MN 55905 USA
[2] Karolinska Inst, Dept Clin Neurosci, Stockholm, Sweden
关键词
aging; ischemia; motor activity; rehabilitation; photothrombosis;
D O I
10.1016/S0197-4580(02)00129-X
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Male Fischer 344 rats aged 3, 6, 12, 18 and 24 months were trained to walk on a narrow beam, then lesioned in the right hindlimb sensorimotor cortex by photothrombosis. Motor performance was measured daily for 60 days using a 7-point rating scale from which deficit scores were calculated. Tissue analysis included lesion volume measurement after Nissl staining. Animals aged 3 and 6 months fully recovered by day 10 and 31, respectively. Animals aged 18 months acquired significant neurological impairment that persisted greater than 60 days. Deficit scores were significantly greater than in groups aged 12, 6 and 3 months. Degenerative morbidity and mortality confounded behavioral study of animals aged 24 months. The duration of neurological impairment after photochemical sensorimotor cortex lesion increased with age. Animals aged 18 months at lesion acquired the greatest chronic impairment. This aged post-acute animal model is clinically relevant to stroke rehabilitation. (C) 2002 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:607 / 614
页数:8
相关论文
共 92 条
[1]   Age and hemisphere effects on dendritic structure [J].
Anderson, B ;
Rutledge, V .
BRAIN, 1996, 119 :1983-1990
[2]   Neurochemical changes in the hippocampus of the Brown Norway rat during aging [J].
Bhatnagar, M ;
Cintra, A ;
Chadi, G ;
Lindberg, J ;
Oitzl, M ;
DeKloet, ER ;
Moller, A ;
Agnati, LF ;
Fuxe, K .
NEUROBIOLOGY OF AGING, 1997, 18 (03) :319-327
[3]  
BJELKE B, 1993, ABSTR SOC NEUROSCI, V19, P1653
[5]  
BRODY H, 1978, ALZHEIMERS DISEASE S, V7, P345
[6]   Neocortical synapse density and braak stage in the lewy body variant of Alzheimer disease: A comparison with classic Alzheimer disease and normal aging [J].
Brown, DF ;
Risser, RC ;
Bigio, EH ;
Tripp, P ;
Stiegler, A ;
Welch, E ;
Eagan, KP ;
Hladik, CL ;
White, CL .
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 1998, 57 (10) :955-960
[7]   Age-related synaptic changes in sensorimotor cortex of the Brown Norway X Fischer 344 rat [J].
Brunso-Bechtold, JK ;
Linville, MC ;
Sonntag, WE .
BRAIN RESEARCH, 2000, 872 (1-2) :125-133
[8]   Hippocampal neuron and synaptophysin-positive bouton number in aging C57BL/6 mice [J].
Calhoun, ME ;
Kurth, D ;
Phinney, AL ;
Long, JM ;
Hengemihle, J ;
Mouton, PR ;
Ingram, DK ;
Jucker, M .
NEUROBIOLOGY OF AGING, 1998, 19 (06) :599-606
[9]   SYNAPTIC LOSS IN COGNITIVELY IMPAIRED AGED RATS IS AMELIORATED BY CHRONIC HUMAN NERVE GROWTH-FACTOR INFUSION [J].
CHEN, KS ;
MASLIAH, E ;
MALLORY, M ;
GAGE, FH .
NEUROSCIENCE, 1995, 68 (01) :19-27
[10]   Dying-back of Purkinje cell dendrites with synapse loss in aging rats [J].
Chen, S ;
Hillman, DE .
JOURNAL OF NEUROCYTOLOGY, 1999, 28 (03) :187-196