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帕金森病进展模型中步态的时空缩放变化

Spatiotemporal scaling changes in gait in a progressive model of Parkinson's disease.

作者信息

Doyle Alex M, Bauer Devyn, Hendrix Claudia, Yu Ying, Nebeck Shane D, Fergus Sinta, Krieg Jordan, Wilmerding Lucius K, Blumenfeld Madeline, Lecy Emily, Spencer Chelsea, Luo Ziling, Sullivan Disa, Brackman Krista, Ross Dylan, Best Sendréa, Verma Ajay, Havel Tyler, Wang Jing, Johnson Luke, Vitek Jerrold L, Johnson Matthew D

机构信息

Department of Neuroscience, University of Minnesota, Minneapolis, MN, United States.

Department of Neurology, University of Minnesota, Minneapolis, MN, United States.

出版信息

Front Neurol. 2022 Dec 13;13:1041934. doi: 10.3389/fneur.2022.1041934. eCollection 2022.

Abstract

OBJECTIVE

Gait dysfunction is one of the most difficult motor signs to treat in patients with Parkinson's disease (PD). Understanding its pathophysiology and developing more effective therapies for parkinsonian gait dysfunction will require preclinical studies that can quantitatively and objectively assess the spatial and temporal features of gait.

DESIGN

We developed a novel system for measuring volitional, naturalistic gait patterns in non-human primates, and then applied the approach to characterize the progression of parkinsonian gait dysfunction across a sequence of 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) treatments that allowed for intrasubject comparisons across mild, moderate, and severe stages.

RESULTS

Parkinsonian gait dysfunction was characterized across treatment levels by a slower stride speed, increased time in both the stance and swing phase of the stride cycle, and decreased cadence that progressively worsened with overall parkinsonian severity. In contrast, decreased stride length occurred most notably in the moderate to severe parkinsonian state.

CONCLUSION

The results suggest that mild parkinsonism in the primate model of PD starts with temporal gait deficits, whereas spatial gait deficits manifest after reaching a more severe parkinsonian state overall. This study provides important context for preclinical studies in non-human primates studying the neurophysiology of and treatments for parkinsonian gait.

摘要

目的

步态功能障碍是帕金森病(PD)患者最难治疗的运动症状之一。要了解其病理生理学并开发出更有效的帕金森病步态功能障碍治疗方法,需要开展能够定量、客观评估步态时空特征的临床前研究。

设计

我们开发了一种用于测量非人类灵长类动物自主、自然步态模式的新型系统,然后应用该方法来表征帕金森病步态功能障碍在一系列1-甲基-4-苯基-1,2,3,6-四氢吡啶(MPTP)治疗过程中的进展情况,这些治疗允许在轻度、中度和重度阶段进行个体内比较。

结果

帕金森病步态功能障碍在各治疗水平上的特征为步速减慢、步幅周期的站立期和摆动期时间增加以及步频降低,且随着帕金森病总体严重程度的增加而逐渐恶化。相比之下,步幅减小最明显出现在中度至重度帕金森病状态。

结论

结果表明,灵长类帕金森病模型中的轻度帕金森病始于步态时间缺陷,而步态空间缺陷在总体达到更严重的帕金森病状态后才会出现。本研究为在非人类灵长类动物中开展的帕金森病步态神经生理学及治疗临床前研究提供了重要背景。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/583c/9792983/d68de7a567bc/fneur-13-1041934-g0001.jpg

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