Toronto Western Research Institute (Division of Brain, Imaging and Behaviour-Systems Neuroscience), UHN, University of Toronto, Toronto, Ontario, Canada.
Hum Brain Mapp. 2009 Dec;30(12):3901-9. doi: 10.1002/hbm.20815.
Patients with advanced Parkinson's disease (PD) develop disabling axial symptoms, including gait disturbances, freezing and postural instability poorly responsive to levodopa replacement therapy. The pedunculopontine nucleus (PPN) is involved in locomotion, control of posture, and behavioral states [i.e. wakefulness, rapid eye movement sleep]. Recent reports suggested that PPN modulation with deep brain stimulation (DBS) may be beneficial in the treatment of axial symptoms. However, the mechanisms underlying these effects are still unknown. We used [(15)O] H(2)O PET to investigate regional cerebral blood flow in three patients with advanced PD who underwent a new experimental surgical procedure with implantation of unilateral PPN-DBS. Patients were studied Off-medication with stimulator Off and On, both at rest and during a self-paced alternating motor task of the lower limbs. We used SPM2 for imaging data analysis, threshold P < 0.05 corrected at the cluster level. Stimulation induced significant regional cerebral blood flow increment in subcortical regions such as the thalamus (P < 0.006), cerebellum (P < 0.001), and midbrain region (P < 0.001) as well as different cortical areas involving medial sensorimotor cortex extending into caudal supplementary motor area (BA 4/6; P < 0.001). PPN-DBS in advanced PD resulted in blood flow and presumably neuronal activity changes in subcortical and cortical areas involved in balance and motor control, including the mesencephalic locomotor region (e.g. PPN) and closely interconnected structures within the cerebello-(rubro)-thalamo-cortical circuit. Whether these findings are associated with the DBS-PPN clinical effect remains to be proven. However, they suggest that PPN modulation may induce functional changes in neural networks associated with the control of lower limb movements.
患有晚期帕金森病(PD)的患者会出现运动障碍等致残性的轴性症状,包括步态障碍、冻结和姿势不稳,这些症状对左旋多巴替代疗法反应不佳。脑桥被盖核(PPN)参与运动、姿势控制和行为状态[即觉醒、快速眼动睡眠]。最近的报告表明,PPN 调制的深部脑刺激(DBS)可能有益于治疗轴性症状。然而,这些效果的机制仍不清楚。我们使用 [(15)O] H(2)O PET 研究了三名接受单侧 PPN-DBS 新实验性手术的晚期 PD 患者的局部脑血流。患者在停药、刺激器关闭和开启的情况下进行研究,在休息时和进行自我调节的下肢交替运动任务时进行研究。我们使用 SPM2 进行成像数据分析,在簇水平上以 P < 0.05 进行校正。刺激诱导了丘脑(P < 0.006)、小脑(P < 0.001)和中脑区域(P < 0.001)等皮质下区域以及涉及内侧感觉运动皮层并延伸到尾侧补充运动区(BA 4/6;P < 0.001)的不同皮质区域的显著局部脑血流增加。在晚期 PD 中,PPN-DBS 导致与平衡和运动控制相关的皮质下和皮质区域的血流和神经元活动变化,包括中脑运动区(如 PPN)和小脑-红核-丘脑皮质回路中的密切相互连接的结构。这些发现是否与 DBS-PPN 的临床效果相关仍有待证明。然而,它们表明 PPN 调制可能会引起与下肢运动控制相关的神经网络的功能变化。