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帕金森病跌倒大鼠模型中的复杂运动控制:纹状体胆碱能中间神经元的双向控制。

Complex Movement Control in a Rat Model of Parkinsonian Falls: Bidirectional Control by Striatal Cholinergic Interneurons.

机构信息

Department of Psychology, University of Michigan, Ann Arbor, Michigan 48103.

Department of Psychology, University of Michigan, Ann Arbor, Michigan 48103

出版信息

J Neurosci. 2020 Jul 29;40(31):6049-6067. doi: 10.1523/JNEUROSCI.0220-20.2020. Epub 2020 Jun 18.

Abstract

Older persons and, more severely, persons with Parkinson's disease (PD) exhibit gait dysfunction, postural instability and a propensity for falls. These dopamine (DA) replacement-resistant symptoms are associated with losses of basal forebrain and striatal cholinergic neurons, suggesting that falls reflect disruption of the corticostriatal transfer of movement-related cues and their striatal integration with movement sequencing. To advance a rodent model of the complex movement deficits of Parkinsonian fallers, here we first demonstrated that male and female rats with dual cortical cholinergic and striatal DA losses (DL rats) exhibit cued turning deficits, modeling the turning deficits seen in these patients. As striatal cholinergic interneurons (ChIs) are positioned to integrate movement cues with gait, and as ChI loss has been associated with falls in PD, we next used this task, as well as a previously established task used to reveal heightened fall rates in DL rats, to broadly test the role of ChIs. Chemogenetic inhibition of ChIs in otherwise intact male and female rats caused cued turning deficits and elevated fall rates. Spontaneous turning was unaffected. Furthermore, chemogenetic stimulation of ChIs in DL rats reduced fall rates and restored cued turning performance. Stimulation of ChIs was relatively more effective in rats with viral transfection spaces situated lateral to the DA depletion areas in the dorsomedial striatum. These results indicate that striatal ChIs are essential for the control of complex movements, and they suggest a therapeutic potential of stimulation of ChIs to restore gait and balance, and to prevent falls in PD. In persons with Parkinson's disease, gait dysfunction and the associated risk for falls do not benefit from dopamine replacement therapy and often result in long-term hospitalization and nursing home placement. Here, we first validated a new task to demonstrate impairments in cued turning behavior in rodents modeling the cholinergic-dopaminergic losses observed in Parkinsonian fallers. We then demonstrated the essential role of striatal cholinergic interneurons for turning behavior as well as for traversing dynamic surfaces and avoiding falls. Stimulation of these interneurons in the rat model rescued turning performance and reduced fall rates. Our findings indicate the feasibility of investigating the neuronal circuitry underling complex movement control in rodents, and that striatal cholinergic interneurons are an essential node of such circuitry.

摘要

老年人,更严重的是帕金森病(PD)患者表现出行走功能障碍、姿势不稳和易跌倒。这些多巴胺(DA)替代治疗抵抗症状与基底前脑和纹状体胆碱能神经元的丧失有关,表明跌倒反映了与运动相关线索的皮质纹状体转移和它们在纹状体与运动序列整合的中断。为了推进帕金森病跌倒者复杂运动缺陷的啮齿动物模型,我们首先证明了皮质胆碱能和纹状体 DA 双重丧失(DL 大鼠)的雄性和雌性大鼠表现出提示转弯缺陷,模拟了这些患者的转弯缺陷。由于纹状体胆碱能中间神经元(ChIs)位于整合运动线索与步态的位置,并且 ChI 丧失与 PD 中的跌倒有关,因此我们接下来使用了该任务以及先前建立的用于揭示 DL 大鼠中跌倒率升高的任务,广泛测试 ChIs 的作用。在其他方面完整的雄性和雌性大鼠中,化学遗传抑制 ChIs 导致提示转弯缺陷和跌倒率升高。自发转弯不受影响。此外,在 DL 大鼠中,化学遗传刺激 ChIs 降低了跌倒率并恢复了提示转弯性能。在病毒转染空间位于背侧纹状体 DA 耗竭区域外侧的大鼠中,刺激 ChIs 的效果相对更有效。这些结果表明纹状体 ChIs 是控制复杂运动的必要条件,并且它们提示刺激 ChIs 以恢复步态和平衡并预防 PD 中的跌倒具有治疗潜力。在帕金森病患者中,步态功能障碍和相关的跌倒风险不能从多巴胺替代治疗中获益,并且经常导致长期住院和疗养院安置。在这里,我们首先验证了一项新任务,以证明在模拟帕金森病跌倒者中观察到的胆碱能-多巴胺丧失的啮齿动物中提示转弯行为的损伤。然后,我们证明了纹状体胆碱能中间神经元对转弯行为以及穿越动态表面和避免跌倒的重要作用。在大鼠模型中刺激这些中间神经元可挽救转弯性能并降低跌倒率。我们的发现表明在啮齿动物中研究复杂运动控制的神经回路的可行性,并且纹状体胆碱能中间神经元是该回路的重要节点。

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