Forced limb-use effects on the behavioral and neurochemical effects of 6-hydroxydopamine

被引:275
作者
Tillerson, JL
Cohen, AD
Philhower, J
Miller, GW
Zigmond, MJ
Schallert, T
机构
[1] Univ Texas, Inst Neurosci, Austin, TX 78712 USA
[2] Univ Texas, Div Pharmacol & Toxicol, Austin, TX 78712 USA
[3] Univ Pittsburgh, Dept Neurol, Pittsburgh, PA 15213 USA
[4] Univ Michigan, Ann Arbor, MI 48109 USA
关键词
motor therapy; Parkinson's disease; neurodegeneration; plasticity; movement; dopamine;
D O I
10.1523/JNEUROSCI.21-12-04427.2001
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Rats with unilateral depletion of striatal dopamine (DA) show marked preferential use of the ipsilateral forelimb. Previous studies have shown that implementation of motor therapy after stroke improves functional outcome (Taub et al., 1999). Thus, we have examined the impact of forced use of the impaired forelimb during or soon after unilateral exposure to the DA neurotoxin 6-hydroxydopamine (6-OHDA). In one group of animals, the nonimpaired forelimb was immobilized using a cast, which forced exclusive use of the impaired limb for the first 7 d after infusion. The animals that received a cast displayed no detectable impairment or asymmetry of limb use, could use the contralateral (impaired) forelimb independently for vertical and lateral weight shifting, and showed no contralateral turning to apomorphine. The behavioral effects were maintained throughout the 60 d of observation. In addition to the behavioral sparing, these animals showed remarkable sparing of striatal DA, its metabolites, and the expression of the vesicular monoamine transporter, suggesting a decrease in the extent of DA neuron degeneration. Behavioral and neurochemical sparing appeared to be complete when the 7 d period of immobilization was initiated immediately after 6-OHDA infusion, only partial sparing was evident when immobilization was initiated 3 d postoperatively, and no sparing was detected when immobilization was initiated 7 d after 6-OHDA treatment. These results suggest that physical therapy may be beneficial in Parkinson's disease.
引用
收藏
页码:4427 / 4435
页数:9
相关论文
共 96 条
[1]  
BILOWIT D S, 1956, Phys Ther Rev, V36, P176
[2]   RESPONSIBILITY OF EXTRASTRIATAL AREAS FOR APPEARANCE OF PSYCHOTIC SYMPTOMS (CLINICAL AND BIOCHEMICAL HUMAN POSTMORTEM FINDINGS [J].
BIRKMAYER, W ;
RIEDERER, P .
JOURNAL OF NEURAL TRANSMISSION, 1975, 37 (02) :175-182
[3]   Movement-related glutamate levels in rat hippocampus, striatum, and sensorimotor cortex [J].
Bland, ST ;
Gonzales, RA ;
Schallert, T .
NEUROSCIENCE LETTERS, 1999, 277 (02) :119-122
[4]   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
[5]  
BORTZ WM, 1981, NEW ENGL J MED, V305, P466
[6]   INJECTIONS OF 6-HYDROXYDOPAMINE IN THE SUBSTANTIA NIGRA OF THE RAT-BRAIN - MORPHOLOGICAL AND BIOCHEMICAL EFFECTS [J].
BUONAMICI, M ;
CERVINI, MA ;
ROSSI, AC ;
SEBASTIANI, L ;
RAFFAELLI, A ;
BAGNOLI, P .
BEHAVIOURAL BRAIN RESEARCH, 1990, 38 (01) :83-95
[7]   Reactive astrocytic responses to denervation in the motor cortex of adult rats are sensitive to manipulations of behavioral experience [J].
Bury, SD ;
Eichhorn, AC ;
Kotzer, CM ;
Jones, TA .
NEUROPHARMACOLOGY, 2000, 39 (05) :743-755
[8]   Effect of 7-nitroindazole on body temperature and methamphetamine-induced dopamine toxicity [J].
Callahan, BT ;
Ricaurte, GA .
NEUROREPORT, 1998, 9 (12) :2691-2695
[9]   Expression of brain-derived neurotrophic factor in cortical neurons is regulated by striatal target area [J].
Canals, JM ;
Checa, N ;
Marco, S ;
Åkerud, P ;
Michels, A ;
Pérez-Navarro, E ;
Tolosa, E ;
Arenas, E ;
Alberch, J .
JOURNAL OF NEUROSCIENCE, 2001, 21 (01) :117-124
[10]   Behavioral and cellular protection of rat dopaminergic neurons by an adenoviral vector encoding glial cell line-derived neurotrophic factor [J].
Choi-Lundberg, DL ;
Lin, Q ;
Schallert, T ;
Crippens, D ;
Davidson, BL ;
Chang, YN ;
Chiang, YWL ;
Qian, JA ;
Bardwaj, L ;
Bohn, MC .
EXPERIMENTAL NEUROLOGY, 1998, 154 (02) :261-275