Roemmich Ryan T, Hack Nawaz, Akbar Umer, Hass Chris J
Kennedy Krieger Institute, Baltimore, MD, United States; Department of Neuroscience, The Johns Hopkins University School of Medicine, United States.
Center for Movement Disorders and Neurorestoration, University of Florida, United States; Department of Neurology, University of Florida, United States.
Behav Brain Res. 2014 Jul 15;268:31-9. doi: 10.1016/j.bbr.2014.03.041. Epub 2014 Mar 31.
Persons with Parkinson's disease (PD) are characterized by multifactorial gait deficits, though the factors which influence the abilities of persons with PD to adapt and store new gait patterns are unclear. The purpose of this study was to investigate the effects of dopaminergic therapy on the abilities of persons with PD to adapt and store gait parameters during split-belt treadmill (SBT) walking. Ten participants with idiopathic PD who were being treated with stable doses of orally-administered dopaminergic therapy participated. All participants performed two randomized testing sessions on separate days: once while optimally-medicated (ON meds) and once after 12-h withdrawal from dopaminergic medication (OFF meds). During each session, locomotor adaptation was investigated as the participants walked on a SBT for 10 min while the belts moved at a 2:1 speed ratio. We assessed locomotor adaptive learning by quantifying: (1) aftereffects during de-adaptation (once the belts returned to tied speeds immediately following SBT walking) and (2) savings during re-adaptation (as the participants repeated the same SBT walking task after washout of aftereffects following the initial SBT task). The withholding of dopaminergic medication diminished step length aftereffects significantly during de-adaptation. However, both locomotor adaptation and savings were unaffected by levodopa. These findings suggest that dopaminergic pathways influence aftereffect storage but do not influence locomotor adaptation or savings within a single session of SBT walking. It appears important that persons with PD should be optimally-medicated if walking on the SBT as gait rehabilitation.
帕金森病(PD)患者具有多因素步态缺陷,然而影响PD患者适应和储存新步态模式能力的因素尚不清楚。本研究的目的是调查多巴胺能治疗对PD患者在分带跑步机(SBT)行走过程中适应和储存步态参数能力的影响。十名正在接受稳定剂量口服多巴胺能治疗的特发性PD患者参与了研究。所有参与者在不同日期进行了两次随机测试:一次是在最佳药物治疗状态下(服药时),一次是在停用多巴胺能药物12小时后(停药时)。在每次测试中,当参与者在SBT上以2:1的速度比行走10分钟时,研究运动适应性。我们通过量化以下指标来评估运动适应性学习:(1)去适应过程中的后效应(SBT行走后皮带立即恢复到绑定时的速度时)和(2)重新适应过程中的节省效应(参与者在初始SBT任务的后效应消除后重复相同的SBT行走任务时)。停用多巴胺能药物在去适应过程中显著减少了步长后效应。然而,左旋多巴对运动适应性和节省效应均无影响。这些发现表明,多巴胺能通路影响后效应的储存,但在单次SBT行走过程中不影响运动适应性或节省效应。如果将SBT行走作为步态康复手段,PD患者进行最佳药物治疗似乎很重要。