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年轻 Ts65Dn 小鼠跑步机跑步能力的出现及步态动力学的定量评估:一种唐氏综合征小鼠模型

Emergence of Treadmill Running Ability and Quantitative Assessment of Gait Dynamics in Young Ts65Dn Mice: A Mouse Model for Down Syndrome.

作者信息

Scott-McKean Jonah J, Jones Ryan, Johnson Mark W, Mier Joyce, Basten Ines A, Stasko Melissa R, Costa Alberto C S

机构信息

Department of Macromolecular Science and Engineering, Case Western Reserve University, Cleveland, OH 44106-6090, USA.

College of Medicine and Life Sciences, The University of Toledo, Toledo, OH 43606-3390, USA.

出版信息

Brain Sci. 2023 Apr 29;13(5):743. doi: 10.3390/brainsci13050743.

Abstract

Down syndrome (DS), which results from the complete or partial trisomy of chromosome 21 (trisomy-21), is the most common genetically defined cause of intellectual disability. Trisomy-21 also produces, or is associated with, many neurodevelopmental phenotypes and neurological comorbidities, including delays and deficits in fine and gross motor development. The Ts65Dn mouse is the most studied animal model for DS and displays the largest known subset of DS-like phenotypes. To date, however, only a small number of developmental phenotypes have been quantitatively defined in these animals. Here, we used a commercially available high-speed, video-based system to record and analyze the gait of Ts65Dn and euploid control mice. Longitudinal treadmill recordings were performed from p17 to p35. One of the main findings was the detection of genotype- and sex-dependent developmental delays in the emergence of consistent, progressive-intensity gait in Ts65Dn mice when compared to control mice. Gait dynamic analysis showed wider normalized front and hind stances in Ts65Dn mice compared to control mice, which may reflect deficits in dynamic postural balance. Ts65Dn mice also displayed statistically significant differences in the variability in several normalized gait measures, which were indicative of deficits in precise motor control in generating gait.

摘要

唐氏综合征(DS)由21号染色体完全或部分三体性(三体-21)导致,是智力残疾最常见的遗传学明确病因。三体-21还会产生或与许多神经发育表型及神经共病相关,包括精细和粗大运动发育的延迟及缺陷。Ts65Dn小鼠是针对DS研究最多的动物模型,展现出已知最大的一组类似DS的表型。然而,迄今为止,这些动物中只有少数发育表型得到了定量界定。在此,我们使用一种商用的基于视频的高速系统来记录和分析Ts65Dn小鼠及正常对照小鼠的步态。从出生后第17天(p17)到第35天(p35)进行纵向跑步机记录。主要发现之一是,与对照小鼠相比,检测到Ts65Dn小鼠在出现一致的、强度逐渐增加的步态时存在基因型和性别依赖性发育延迟。步态动力学分析显示,与对照小鼠相比,Ts65Dn小鼠的归一化前肢和后肢步幅更宽,这可能反映了动态姿势平衡方面的缺陷。Ts65Dn小鼠在几种归一化步态指标的变异性方面也表现出统计学上的显著差异,这表明在产生步态时精确运动控制存在缺陷。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0c5/10216633/059be8c5efb0/brainsci-13-00743-g0A1.jpg

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