Department of Physiology and Biophysics, University of Colorado School of Medicine, Aurora, Colorado.
Department of Neurosurgery, University of Colorado School of Medicine, Aurora, Colorado.
J Neurophysiol. 2021 Oct 1;126(4):1248-1264. doi: 10.1152/jn.00001.2021. Epub 2021 Aug 18.
Parkinsonian motor deficits are associated with elevated inhibitory output from the basal ganglia (BG). However, several features of Parkinson's disease (PD) have not been accounted for by this simple "classical rate model" framework, including the observation in patients with PD that movements guided by external stimuli are less impaired than otherwise identical movements generated based on internal goals. Is this difference due to divergent processing within the BG itself or due to the recruitment of extra-BG pathways by sensory processing? In addition, surprisingly little is known about precisely when, in the sequence from selecting to executing movements, BG output is altered by PD. Here, we address these questions by recording activity in the substantia nigra pars reticulata (SNr), a key BG output nucleus, in hemiparkinsonian mice performing a well-controlled behavioral task requiring stimulus-guided and internally specified directional movements. We found that hemiparkinsonian mice exhibited a bias ipsilateral to the side of dopaminergic cell loss that was stronger when movements were internally specified rather than stimulus guided, consistent with clinical observations in patients with Parkinson's disease. We further found that changes in parkinsonian SNr activity during movement preparation were consistent with the ipsilateral behavioral bias, as well as its greater magnitude for internally specified movements. Although these findings are inconsistent with some aspects of the classical rate model, they are accounted for by a related "directional rate model" positing that SNr output phasically overinhibits motor output in a direction-specific manner. These results suggest that parkinsonian changes in BG output underlying movement preparation contribute to the greater deficit in internally specified than stimulus-guided movements. Movements of patients with Parkinson's disease are often less impaired when guided by external stimuli than when generated based on internal goals. Whether this effect is due to distinct processing in the basal ganglia (BG) or due to compensation from other motor pathways is an open question with therapeutic implications. We recorded BG output in behaving parkinsonian mice and found that BG activity during movement preparation was consistent with the differences between these forms of movement.
帕金森病的运动缺陷与基底神经节(BG)抑制性输出增加有关。然而,这个简单的“经典速率模型”框架并不能解释帕金森病的几个特征,包括观察到帕金森病患者在受外部刺激引导的运动中受损程度小于其他基于内部目标生成的运动。这种差异是由于 BG 本身的处理方式不同,还是由于感觉处理过程中额外的 BG 通路的募集?此外,人们对帕金森病患者在从选择到执行运动的序列中,BG 输出何时发生改变知之甚少。在这里,我们通过记录半帕金森病小鼠在执行一项需要刺激引导和内部指定方向运动的受控行为任务时,脑黑质网状部(SNr)中的活动来解决这些问题。我们发现,半帕金森病小鼠表现出一种向多巴胺能细胞缺失侧的偏向,这种偏向在内部指定运动而不是刺激引导运动时更强,这与帕金森病患者的临床观察一致。我们进一步发现,帕金森病 SNr 活动在运动准备期间的变化与同侧行为偏向一致,并且对于内部指定运动,其变化幅度更大。尽管这些发现与经典速率模型的某些方面不一致,但它们与相关的“方向速率模型”一致,该模型假设 SNr 输出以方向特异性的方式阶段性地过度抑制运动输出。这些结果表明,运动准备过程中 BG 输出的帕金森病变化导致内部指定运动比刺激引导运动的缺陷更大。帕金森病患者的运动通常在受外部刺激引导时比基于内部目标生成时受损程度更小。这种效应是由于基底神经节(BG)中的不同处理方式还是由于其他运动通路的补偿,这是一个具有治疗意义的悬而未决的问题。我们在行为性帕金森病小鼠中记录了 BG 输出,发现运动准备期间的 BG 活动与这两种运动形式之间的差异一致。