Konrad C, Jansen A, Henningsen H, Sommer J, Turski P A, Brooks B R, Knecht S
Department of Psychiatry and Psychotherapy, IZKF, University of Muenster, Albert-Schweitzer-Str. 11, 48149 Muenster, Germany.
Exp Brain Res. 2006 Jul;172(3):361-9. doi: 10.1007/s00221-006-0352-7. Epub 2006 Mar 25.
The cerebral cortex reorganizes in response to central or peripheral lesions. Although basal ganglia and cerebellum are key components of the network dedicated to movement control, their role in motor reorganization remains elusive. We therefore tested if slowly progressive neurodegenerative motor disease alters the subcortical functional anatomy of the basal ganglia-thalamo-cerebellar circuitry. Ten patients with amyotrophic lateral sclerosis (ALS) and ten healthy controls underwent functional magnetic resonance imaging (fMRI), while executing a simple finger flexion task. Cued by an acoustic trigger, they squeezed a handgrip force transducer with their right hand at 10% of their maximum voluntary contraction force. Movement frequency, amplitude, and force were controlled. Statistical parametric mapping of task-related BOLD-response revealed increased activation in ALS patients as compared to healthy controls. The main activation increases were found in the supplementary motor area, basal ganglia, brainstem, and cerebellum. These findings suggest that degeneration of cortical and spinal motor neurons in ALS leads to a recruitment of subcortical motor structures. These subcortical activation patterns strongly resemble functional activation in motor learning and might therefore represent adaptations of cortico-subcortical motor loops as a - albeit finally ineffective - mechanism to compensate for the ongoing loss of motor neurons in ALS.
大脑皮层会因中枢或外周损伤而发生重组。尽管基底神经节和小脑是运动控制网络的关键组成部分,但其在运动重组中的作用仍不明确。因此,我们测试了缓慢进展性神经退行性运动疾病是否会改变基底神经节 - 丘脑 - 小脑回路的皮质下功能解剖结构。10例肌萎缩侧索硬化症(ALS)患者和10名健康对照者在执行简单的手指屈曲任务时接受了功能磁共振成像(fMRI)检查。在声音触发提示下,他们用右手以最大自主收缩力的10%挤压手握力传感器。运动频率、幅度和力量均受到控制。与任务相关的血氧水平依赖(BOLD)反应的统计参数映射显示,与健康对照者相比,ALS患者的激活增加。主要激活增加区域见于辅助运动区、基底神经节、脑干和小脑。这些发现表明,ALS患者皮质和脊髓运动神经元的退化导致皮质下运动结构的募集。这些皮质下激活模式与运动学习中的功能激活非常相似,因此可能代表了皮质 - 皮质下运动环路的适应性变化,作为一种尽管最终无效但仍试图补偿ALS中持续的运动神经元损失的机制。