Functional Neuroimaging, Cognitive, and Mobility Laboratory, Department of Radiology, Division of Nuclear Medicine, University of Michigan, 24 Frank Lloyd Wright Dr, Box #362, Ann Arbor, MI 48105, USA.
Curr Neurol Neurosci Rep. 2013 Sep;13(9):377. doi: 10.1007/s11910-013-0377-9.
There is increasing interest in the clinical effects of cholinergic basal forebrain and tegmental pedunculopontine complex (PPN) projection degeneration in Parkinson's disease (PD). Recent evidence supports an expanded role beyond cognitive impairment, including effects on olfaction, mood, REM sleep behavior disorder, and motor functions. Cholinergic denervation is variable in PD without dementia and may contribute to clinical symptom heterogeneity. Early in vivo imaging evidence that impaired cholinergic integrity of the PPN associates with frequent falling in PD is now confirmed by human post-mortem evidence. Brainstem cholinergic lesioning studies in primates confirm the role of the PPN in mobility impairment. Degeneration of basal forebrain cholinergic projections correlates with decreased walking speed. Cumulatively, these findings provide evidence for a new paradigm to explain dopamine-resistant features of mobility impairments in PD. Recognition of the increased clinical role of cholinergic system degeneration may motivate new research to expand indications for cholinergic therapy in PD.
人们对帕金森病(PD)中胆碱能基底前脑和被盖脚桥核(PPN)投射退化的临床影响越来越感兴趣。最近的证据支持其作用不仅限于认知障碍,还包括对嗅觉、情绪、快速眼动睡眠行为障碍和运动功能的影响。PD 不伴痴呆患者的胆碱能神经支配具有变异性,可能导致临床症状异质性。早期的活体成像证据表明,PPN 胆碱能完整性受损与 PD 患者经常跌倒有关,现在已经被人体死后证据所证实。灵长类动物的脑干胆碱能损伤研究证实了 PPN 在运动障碍中的作用。基底前脑胆碱能投射的退化与行走速度下降有关。综上所述,这些发现为解释 PD 中运动障碍对多巴胺抵抗的新范式提供了证据。认识到胆碱能系统退化的临床作用增加可能会促使新的研究扩大 PD 中胆碱能治疗的适应症。