首页> 美国卫生研究院文献>The Journal of Neuroscience >Modeling Fall Propensity in Parkinsons Disease: Deficits in the Attentional Control of Complex Movements in Rats with Cortical-Cholinergic and Striatal–Dopaminergic Deafferentation
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Modeling Fall Propensity in Parkinsons Disease: Deficits in the Attentional Control of Complex Movements in Rats with Cortical-Cholinergic and Striatal–Dopaminergic Deafferentation

机译:帕金森氏病的秋季倾向建模:皮质胆碱能和纹状体多巴胺能脱除咖啡因的大鼠复杂运动注意控制的缺陷

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摘要

Cognitive symptoms, complex movement deficits, and increased propensity for falls are interrelated and levodopa-unresponsive symptoms in patients with Parkinson's disease (PD). We developed a test system for the assessment of fall propensity in rats and tested the hypothesis that interactions between loss of cortical cholinergic and striatal dopaminergic afferents increase fall propensity. Rats were trained to traverse stationary and rotating rods, placed horizontally or at inclines, and while exposed to distractors. Rats also performed an operant Sustained Attention Task (SAT). Partial cortical cholinergic and/or caudate dopaminergic deafferentation were produced by bilateral infusions of 192 IgG-saporin (SAP) into the basal forebrain and/or 6-hydroxydopamine (6-OHDA) into the caudate nucleus, respectively, modeling the lesions seen in early PD. Rats with dual cholinergic–dopaminergic lesions (DL) fell more frequently than SAP or 6-OHDA rats. Falls in DL rats were associated with incomplete rebalancing after slips and low traversal speed. Ladder rung walking and pasta handling performance did not indicate sensorimotor deficits. SAT performance was impaired in DL and SAP rats; however, SAT performance and falls were correlated only in DL rats. Furthermore, in DL rats, but not in rats with only dopaminergic lesions, the placement and size of dopaminergic lesion correlated significantly with fall rates. The results support the hypothesis that after dual cholinergic–dopaminergic lesions, attentional resources can no longer be recruited to compensate for diminished striatal control of complex movement, thereby “unmasking” impaired striatal control of complex movements and yielding falls.
机译:帕金森病(PD)患者的认知症状,复杂的运动缺陷和跌倒倾向增加是相互关联的,左旋多巴无反应的症状。我们开发了一种用于评估大鼠跌倒倾向的测试系统,并测试了以下假设的假设:皮层胆碱能和纹状体多巴胺能传入缺失之间的相互作用会增加跌倒倾向。训练大鼠横穿固定棒和旋转棒,使其水平或倾斜放置,并使其暴露于牵张器。大鼠还执行了操作性持续注意任务(SAT)。部分皮质胆碱能和/或尾巴多巴胺能脱除咖啡因是通过分别向基底前脑双边注入192个IgG-saporin(SAP)和/或将6-羟基多巴胺(6-OHDA)注入尾状核而产生的,模拟了早期发现的病变PD。胆碱能-多巴胺能双重损伤(DL)的大鼠比SAP或6-OHDA的大鼠跌倒的频率更高。 DL大鼠的跌倒与滑倒后的不完全平衡和低穿越速度有关。梯级行走和面食处理性能未表明感觉运动缺陷。 DL和SAP大鼠的SAT表现受损;然而,仅DL大鼠的SAT表现和跌倒相关。此外,在DL大鼠中,而不在仅具有多巴胺能性病变的大鼠中,多巴胺能性病变的位置和大小与跌倒率显着相关。结果支持这样的假说:在胆碱能-多巴胺能双重病变后,不能再募集注意力资源来补偿复杂运动的纹状体控制的减弱,从而“掩盖”复杂运动的纹状体控制的削弱和屈服性下降。

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