The effect of voluntary exercise exposure on histological and neurobehavioral outcomes after ischemic brain injury in the rat

被引:57
作者
Marin, R
Williams, A
Hale, S
Burge, B
Mense, M
Bauman, R
Tortella, F
机构
[1] Walter Reed Army Inst Res, Dept Army, Silver Spring, MD 20910 USA
[2] Walter Reed Army Med Ctr, Dept Army, Washington, DC 20307 USA
关键词
exercise; recovery; cerebral infarction; forelimb placing; synaptophysin; behavioral deficits; outcome; rat; MCAo;
D O I
10.1016/j.physbeh.2003.06.001
中图分类号
B84 [心理学];
学科分类号
04 ; 0402 ;
摘要
Physical activity can induce neuroplastic adaptations and improve outcomes after cerebral injury. To determine if these outcomes are dependent on the type and timing of physical rehabilitation and the particular outcome/endpoint being tested, we evaluated the effect of voluntary exercise exposure beginning 24 h after cerebral ischemic injury on behavioral, physiological, and histological outcomes. In an observer-blinded fashion, Sprague-Dawley (300 g) male rats were allocated to three groups [sham-exercise (SHAM), stroke-exercise (SE), stroke-no exercise (SNE)] before a 1-h right middle cerebral artery occlusion (MCAo). Running wheels were used for voluntary exercise. A significant difference was found at I week post-infarction between the SNE and SE, with SNE showing worst neurological scores and higher number of foot faults. In addition, nearly 20% more of the SE animals regained their pre-MCAo weight by 7 days. These differences were not as evident at 2 weeks. No differences were found between the three groups in the paw preference test, wheel activity, and body temperature, as well as between SNE and SE with regards to infarct or hemispheric volumes, body weight, synaptophysin staining, and electroencephalography (EEG) testing. Within-group comparisons showed no relationships between infarct volume and foot faults, neurological scores, or exercise level. We conclude that (1) unlike behavioral outcomes, physiological and histological outcomes may not be influenced by the introduction of voluntary exercise once lesion maturation has occurred at 24 h, and (2) repetitive outcomes testing can obscure findings in rat models of cerebral ischemic injury. Published by Elsevier Inc.
引用
收藏
页码:167 / 175
页数:9
相关论文
共 66 条
[21]   A COMPARISON OF THE EARLY DEVELOPMENT OF ISCHEMIC DAMAGE FOLLOWING PERMANENT MIDDLE CEREBRAL-ARTERY OCCLUSION IN RATS AS ASSESSED USING MAGNETIC-RESONANCE-IMAGING AND HISTOLOGY [J].
GILL, R ;
SIBSON, NR ;
HATFIELD, RH ;
BURDETT, NG ;
CARPENTER, TA ;
HALL, LD ;
PICKARD, JD .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 1995, 15 (01) :1-11
[22]   INFLUENCE OF AN ENRICHED ENVIRONMENT AND CORTICAL GRAFTING ON FUNCTIONAL OUTCOME IN BRAIN INFARCTS OF ADULT-RATS [J].
GRABOWSKI, M ;
SORENSEN, JC ;
MATTSSON, B ;
ZIMMER, J ;
JOHANSSON, BB .
EXPERIMENTAL NEUROLOGY, 1995, 133 (01) :96-102
[23]   High-resolution EEG in poststroke hemiparesis can identify ipsilateral generators during motor tasks [J].
Green, JB ;
Bialy, Y ;
Sora, E ;
Ricamato, A .
STROKE, 1999, 30 (12) :2659-2665
[24]   Use-dependent exacerbation of brain damage occurs during an early post-lesion vulnerable period [J].
Humm, JL ;
Kozlowski, DA ;
James, DC ;
Gotts, JE ;
Schallert, T .
BRAIN RESEARCH, 1998, 783 (02) :286-292
[25]   Adenosine kinase inhibition protects brain against transient focal ischemia in rats [J].
Jiang, N ;
Kowaluk, EA ;
Lee, CH ;
Mazdiyasni, H ;
Chopp, M .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1997, 320 (2-3) :131-137
[26]   Environment, social interaction, and physical activity as determinants of functional outcome after cerebral infarction in the rat [J].
Johansson, BB ;
Ohlsson, AL .
EXPERIMENTAL NEUROLOGY, 1996, 139 (02) :322-327
[27]   Brain plasticity and stroke rehabilitation - The Willis Lecture [J].
Johansson, BB .
STROKE, 2000, 31 (01) :223-230
[28]  
Jones TA, 1999, J NEUROSCI, V19, P10153
[29]   PHYSICAL-ACTIVITY AND STROKE RISK - THE FRAMINGHAM-STUDY [J].
KIELY, DK ;
WOLF, PA ;
CUPPLES, LA ;
BEISER, AS ;
KANNEL, WB .
AMERICAN JOURNAL OF EPIDEMIOLOGY, 1994, 140 (07) :608-620
[30]  
Kozlowski DA, 1996, J NEUROSCI, V16, P4776