Early exclusive use of the affected forelimb after moderate transient focal ischemia in rats - Functional and anatomic outcome

被引:151
作者
Bland, ST
Schallert, T
Strong, R
Aronowski, J
Grotta, JC
机构
[1] Univ Texas, Dept Psychol, Austin, TX 78712 USA
[2] Univ Texas, Sch Med, Dept Neurol, Houston, TX USA
关键词
middle cerebral artery occlusion; motor activity; stroke; experimental; rats;
D O I
10.1161/01.STR.31.5.1144
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background and Purpose-Previous work by researchers in our laboratory has shown that in the rat, the exclusive use of the affected forelimb during an early critical period exaggerates lesion volume and retards functional recovery after electrolytic lesions of the forelimb sensorimotor cortex. In the present study, we examined the effects of exclusive use of the affected forelimb after middle cerebral artery occlusion (MCAO). Methods-Ischemia of moderate severity was produced in male Long-Evans rats through 45 minutes of occlusion of the left middle cerebral and both common carotid arteries. Exclusive use of either the affected or unaffected forelimb was forced through immobilization of either the ipsilateral (MCAO+ipsi) or contralateral (MCAO+contra) forelimb, respectively, for 10 days in a plaster cast, or the animal was left uncasted (MCAO+nocast). Sham surgeries were performed, and animals were also casted for 10 days or left uncasted. Sensorimotor testing was performed during days 17 to 38. At the end of sensorimotor testing, cognitive performance was tested with use of the Morris water maze. In a separate experiment, temperatures and corticosterone levels were measured during the 10-day period after 45-minute ischemia and casting. Results-The MCAO+ipsi group performed worse on sensorimotor tasks than the MCAO+contra, MCAO+nocast, and sham groups. Infarct volume was significantly larger in the MCAO+ipsi group than in the sham and MCAO+contra groups but not in the MCAO+nocast group. No group differences were found with the Morris water maze, and no group differences were found in either temperature or plasma corticosterone level. Conclusion-The exclusive use of the affected forelimb immediately after focal ischemia has detrimental effects on sensorimotor function that cannot be attributed to hyperthermia or stress.
引用
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页码:1144 / 1151
页数:8
相关论文
共 51 条
  • [31] Neural substrates for the effects of rehabilitative training on motor recovery after ischemic infarct
    Nudo, RJ
    Wise, BM
    SiFuentes, F
    Milliken, GW
    [J]. SCIENCE, 1996, 272 (5269) : 1791 - 1794
  • [32] ENVIRONMENT INFLUENCES FUNCTIONAL OUTCOME OF CEREBRAL INFARCTION IN RATS
    OHLSSON, AL
    JOHANSSON, BB
    [J]. STROKE, 1995, 26 (04) : 644 - 649
  • [33] The neuropsychology of spatial cognition in the rat
    Poucet, B
    Benhamou, S
    [J]. CRITICAL REVIEWS IN NEUROBIOLOGY, 1997, 11 (2-3): : 101 - 120
  • [34] Long-term changes of ionotropic glutamate and GABA receptors after unilateral permanent focal cerebral ischemia in the mouse brain
    Qü, M
    Mittmann, T
    Luhmann, HJ
    Schleicher, A
    Zilles, K
    [J]. NEUROSCIENCE, 1998, 85 (01) : 29 - 43
  • [35] Early training may exacerbate brain damage after focal brain ischemia in the rat
    Risedal, A
    Zeng, JS
    Johansson, BB
    [J]. JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 1999, 19 (09) : 997 - 1003
  • [36] GLUCOCORTICOIDS POTENTIATE ISCHEMIC-INJURY TO NEURONS - THERAPEUTIC IMPLICATIONS
    SAPOLSKY, RM
    PULSINELLI, WA
    [J]. SCIENCE, 1985, 229 (4720) : 1397 - 1400
  • [37] SAPOLSKY RM, 1990, PROG BRAIN RES, V86, P13
  • [38] SCHALLERT T, 1998, CEREBROVASC DIS, P611
  • [39] Neuronal hyperexcitability and reduction of GABA(A)-receptor expression in the surround of cerebral photothrombosis
    Schiene, K
    Bruehl, C
    Zilles, K
    Qu, MS
    Hagemann, G
    Kraemer, M
    Witte, OW
    [J]. JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 1996, 16 (05) : 906 - 914
  • [40] Metyrapone, an inhibitor of glucocorticoid production, reduces brain injury induced by focal and global ischemia and seizures
    SmithSwintosky, VL
    Pettigrew, LC
    Sapolsky, RM
    Phares, C
    Craddock, SD
    Brooke, SM
    Mattson, MP
    [J]. JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 1996, 16 (04) : 585 - 598