Navya Nair, Grace Hey, Alexander Becsey, Tara Kari, Xavier Becsey, Julia Root, Vinata Vedam-Mai
{"title":"Temporal and Spatial Dynamics of Motor Dysfunction in Preclinical Parkinson's Disease and Aging.","authors":"Navya Nair, Grace Hey, Alexander Becsey, Tara Kari, Xavier Becsey, Julia Root, Vinata Vedam-Mai","doi":"10.20900/jpbs.20250009","DOIUrl":null,"url":null,"abstract":"<p><p>Gait assessments have been performed in several murine models of Parkinson's Disease (PD), but the M83<sup>+/-</sup> mouse model of PD has been relatively understudied in this context. Metrics of gait swing, stride length and frequency, and ataxia were collected in M83<sup>+/-</sup> mice with peripheral injections of α-syn preformed fibrils (PFF) and in aged M83<sup>+/-</sup> mice without fibrils using the DigiGait<sup>™</sup> system. PFF-mice showed significantly decreased swing in all limbs (0.11 ± 0.02 vs. 0.13 ± 0.03, <i>p</i> = 0.007) compared to age-matched controls. Stride frequency was significantly increased in all limbs (3.9 ± 0.4 vs. 3.0 ± 0.5, <i>p</i> = 0.010) of PFF-treated mice. Swing was significantly greater in the hindlimbs of young M83<sup>+/-</sup>+PFF mice compared to aged M83<sup>+/-</sup> mice (0.11(0.5) vs. 0.08 (0.3), <i>p</i> = 0.015). Ataxia was significantly higher in young M83<sup>+/-</sup>+PFF mice compared to control for forelimbs (1.1 ± 1.0 vs. 0.6 ± 0.5, <i>p</i> = 0.027), hindlimbs (0.9 ± 1.0 vs. 0.3 ± 0.2, <i>p</i> = 0.016), and all limbs (1.0 ± 1.0 vs. 0.3 ± 0.5, <i>p</i> = 0.015). M83<sup>+/-</sup> mice demonstrate significant gait abnormalities consistent with features of PD. This study supports the utility of the M83<sup>+/-</sup> murine model for preclinical gait analyses in PD.</p>","PeriodicalId":73912,"journal":{"name":"Journal of psychiatry and brain science","volume":"10 4","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12419535/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of psychiatry and brain science","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.20900/jpbs.20250009","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/8/6 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Gait assessments have been performed in several murine models of Parkinson's Disease (PD), but the M83+/- mouse model of PD has been relatively understudied in this context. Metrics of gait swing, stride length and frequency, and ataxia were collected in M83+/- mice with peripheral injections of α-syn preformed fibrils (PFF) and in aged M83+/- mice without fibrils using the DigiGait™ system. PFF-mice showed significantly decreased swing in all limbs (0.11 ± 0.02 vs. 0.13 ± 0.03, p = 0.007) compared to age-matched controls. Stride frequency was significantly increased in all limbs (3.9 ± 0.4 vs. 3.0 ± 0.5, p = 0.010) of PFF-treated mice. Swing was significantly greater in the hindlimbs of young M83+/-+PFF mice compared to aged M83+/- mice (0.11(0.5) vs. 0.08 (0.3), p = 0.015). Ataxia was significantly higher in young M83+/-+PFF mice compared to control for forelimbs (1.1 ± 1.0 vs. 0.6 ± 0.5, p = 0.027), hindlimbs (0.9 ± 1.0 vs. 0.3 ± 0.2, p = 0.016), and all limbs (1.0 ± 1.0 vs. 0.3 ± 0.5, p = 0.015). M83+/- mice demonstrate significant gait abnormalities consistent with features of PD. This study supports the utility of the M83+/- murine model for preclinical gait analyses in PD.