Feigin A, Ghilardi M F, Fukuda M, Mentis M J, Dhawan V, Barnes A, Ghez C P, Eidelberg D
Center for Neurosciences, North Shore-LIJ Research Institute, Manhasset, NY 11030, USA.
Neurology. 2002 Jul 23;59(2):220-6. doi: 10.1212/wnl.59.2.220.
Clinical improvement with levodopa therapy for PD is associated with specific regional changes in cerebral glucose metabolism. However, it is unknown how these effects of treatment in the resting state relate to alterations in brain function that occur during movement. In this study, the authors used PET to assess the effects of levodopa on motor activation responses and determined how these changes related to on-line recordings of movement speed and accuracy.
Seven right-handed PD patients were scanned with H(2)15O/PET while performing a predictable paced sequence of reaching movements and while observing the same screen displays and tones. PET studies were performed during "on" and "off" states with an individually titrated constant rate levodopa infusion; movements were kinematically controlled across treatment conditions.
Levodopa improved "off" state UPDRS motor ratings (34%; p < 0.006) and movement time (18%; p = 0.001). Spatial errors worsened during levodopa infusion (24%; p = 0.02). Concurrent regional cerebral blood flow (rCBF) recordings revealed significant enhancement of motor activation responses in the posterior putamen bilaterally (p < 0.001), left ventral thalamus (p < 0.002), and pons (p < 0.005). Movement time improvement with treatment correlated with rCBF increases in the left globus pallidus and left ventral thalamus (p < 0.01). By contrast, the increase in spatial errors correlated with rCBF increases in the cerebellar vermis (p < 0.01).
These results suggest that levodopa infusion may improve aspects of motor performance while worsening others. Different components of the motor cortico-striato-pallido-thalamo-cortical loop and related pathways may underlie motor improvement and adverse motoric effects of levodopa therapy for PD.
帕金森病(PD)患者接受左旋多巴治疗后的临床改善与脑葡萄糖代谢的特定区域变化相关。然而,静息状态下治疗的这些效果与运动期间发生的脑功能改变之间的关系尚不清楚。在本研究中,作者使用正电子发射断层扫描(PET)评估左旋多巴对运动激活反应的影响,并确定这些变化与运动速度和准确性的在线记录之间的关系。
7名右利手PD患者在进行可预测节奏的伸手动作序列以及观察相同的屏幕显示和音调时,接受H(2)15O/PET扫描。PET研究在“开”和“关”状态下进行,采用个体化滴定的恒速左旋多巴输注;在不同治疗条件下对运动进行运动学控制。
左旋多巴改善了“关”状态下的统一帕金森病评定量表(UPDRS)运动评分(提高34%;p < 0.006)和运动时间(缩短18%;p = 0.001)。在左旋多巴输注期间,空间误差恶化(增加24%;p = 0.02)。同时进行的局部脑血流量(rCBF)记录显示,双侧壳核后部(p < 0.001)、左侧腹侧丘脑(p < 0.002)和脑桥(p < 0.005)的运动激活反应显著增强。治疗后运动时间的改善与左侧苍白球和左侧腹侧丘脑的rCBF增加相关(p < 0.01)。相比之下,空间误差的增加与小脑蚓部的rCBF增加相关(p < 0.01)。
这些结果表明,左旋多巴输注可能改善运动表现的某些方面,同时使其他方面恶化。运动皮质-纹状体-苍白球-丘脑-皮质环路及相关通路的不同组成部分可能是左旋多巴治疗PD的运动改善和不良运动效应的基础。