Negrotti A, Secchi C, Gentilucci M
Dipartimento di Neuroscienze, Sezione di Neurologia, Università di Parma, Italy.
Neuropsychologia. 2005;43(3):450-9. doi: 10.1016/j.neuropsychologia.2004.06.009.
The present study aimed to determine whether the bradykinesia of Parkinson's disease (PD) patients during the execution of reaching-grasping movements (i) is related to an impaired implementation of movement parameters and (ii) selectively involves the control of reach and/or grasp movements. We compared the kinematics of reaching to grasp of differently sized objects placed at different positions, among PD patients in the early stage of disease (ESPD), in the advanced stage of disease (ASPD) without L-dopa medication (off-state), and in healthy controls. In addition, we analysed the effects of L-dopa replacement therapy by comparing the kinematics of the patients in the advanced stage of disease after L-dopa administration with those of the other groups. Bradykinesia increased with disease progression, but only in the initial phases of the reach and grasp components. However at both stages of the disease, the kinematics of reaching and grasping responded to extrinsic and intrinsic object properties just as in controls. L-dopa administration improved the performance of PD patients, though this was more evident for the reach than for the grasp. We suggest that the basal ganglia (BG) are involved in implementing kinematic parameters, but neither (or only marginally) in the initial movement parameterization itself, nor in the on-line control of movement. Specifically, the BG dysfunction in PD induces a slowed implementation of movement parameters. The lack of effect of L-dopa administration on grasp kinematics may be because the motor control of distal effectors is less represented in the motor circuitry formed by the supplementary motor area (SMA), thalamus and BG.
本研究旨在确定帕金森病(PD)患者在进行伸手抓握动作时的运动迟缓:(i)是否与运动参数的执行受损有关;(ii)是否选择性地涉及对伸手和/或抓握动作的控制。我们比较了疾病早期(ESPD)、未服用左旋多巴药物(关期)的疾病晚期(ASPD)的PD患者以及健康对照者在抓取放置于不同位置的不同大小物体时的伸手运动学。此外,我们通过比较疾病晚期患者服用左旋多巴后的运动学与其他组的运动学,分析了左旋多巴替代疗法的效果。运动迟缓随疾病进展而增加,但仅在伸手和抓握动作的初始阶段。然而,在疾病的两个阶段,伸手和抓握的运动学对物体的外在和内在属性的反应与对照组相同。服用左旋多巴改善了PD患者的表现,尽管对伸手动作的改善比对抓握动作更明显。我们认为基底神经节(BG)参与运动学参数的执行,但既不(或仅在边缘程度上)参与初始运动参数的设定本身,也不参与运动的在线控制。具体而言,PD中的BG功能障碍导致运动参数的执行减慢。服用左旋多巴对抓握运动学缺乏影响可能是因为在由辅助运动区(SMA)、丘脑和BG形成的运动回路中,远端效应器的运动控制占比更低。