• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

用于神经肌肉疾病小鼠模型行为表型分析的低成本步态分析

Low-Cost Gait Analysis for Behavioral Phenotyping of Mouse Models of Neuromuscular Disease.

作者信息

Wertman Virginia, Gromova Anastasia, La Spada Albert R, Cortes Constanza J

机构信息

Department of Neurology, Duke University School of Medicine; Duke Center for Neurodegeneration & Neurotherapeutics, Duke University School of Medicine.

Department of Neurology, Duke University School of Medicine; Duke Center for Neurodegeneration & Neurotherapeutics, Duke University School of Medicine; Biomedical Sciences Graduate Program, University of California San Diego.

出版信息

J Vis Exp. 2019 Jul 18(149). doi: 10.3791/59878.

DOI:10.3791/59878
PMID:31380846
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7553151/
Abstract

Measurement of animal locomotion is a common behavioral tool used to describe the phenotype of a given disease, injury, or drug model. The low-cost method of gait analysis demonstrated here is a simple but effective measure of gait abnormalities in murine models. Footprints are analyzed by painting a mouse's feet with non-toxic washable paint and allowing the subject to walk through a tunnel on a sheet of paper. The design of the testing tunnel takes advantage of natural mouse behavior and their affinity for small dark places. The stride length, stride width, and toe spread of each mouse is easily measured using a ruler and a pencil. This is a well-established and reliable method, and it generates several metrics that are analogous to digital systems. This approach is sensitive enough to detect changes in stride early in phenotype presentation, and due to its non-invasive approach, it allows for testing of groups across life-span or phenotypic presentation.

摘要

测量动物运动是一种常用的行为工具,用于描述特定疾病、损伤或药物模型的表型。这里展示的低成本步态分析方法是一种简单但有效的测量小鼠模型步态异常的方法。通过用无毒可洗涂料涂抹小鼠的足部,然后让其在一张纸上的隧道中行走来分析足迹。测试隧道的设计利用了小鼠的自然行为及其对小而黑暗空间的偏好。使用尺子和铅笔可以轻松测量每只小鼠的步长、步宽和脚趾间距。这是一种成熟且可靠的方法,它生成的几个指标类似于数字系统。这种方法足够灵敏,能够在表型出现早期检测到步幅的变化,并且由于其非侵入性,它允许对不同寿命阶段或表型的群体进行测试。

相似文献

1
Low-Cost Gait Analysis for Behavioral Phenotyping of Mouse Models of Neuromuscular Disease.用于神经肌肉疾病小鼠模型行为表型分析的低成本步态分析
J Vis Exp. 2019 Jul 18(149). doi: 10.3791/59878.
2
Analysis of locomotor behavior in the German Mouse Clinic.德国鼠科临床中的运动行为分析。
J Neurosci Methods. 2018 Apr 15;300:77-91. doi: 10.1016/j.jneumeth.2017.05.005. Epub 2017 May 5.
3
Automated gait analysis in the open-field test for laboratory mice.实验室小鼠旷场试验中的自动步态分析
Behav Res Methods. 2009 Feb;41(1):148-153. doi: 10.3758/BRM.41.1.148.
4
Computer-aided identification of degenerative neuromuscular diseases based on gait dynamics and ensemble decision tree classifiers.基于步态动力学和集成决策树分类器的退行性神经肌肉疾病的计算机辅助识别。
PLoS One. 2021 Jun 4;16(6):e0252380. doi: 10.1371/journal.pone.0252380. eCollection 2021.
5
Validity and Reproducibility of Inertial Physilog Sensors for Spatiotemporal Gait Analysis in Patients With Stroke.惯性生理传感器在脑卒中患者时空步态分析中的有效性和可重复性。
IEEE Trans Neural Syst Rehabil Eng. 2019 Sep;27(9):1865-1874. doi: 10.1109/TNSRE.2019.2930751. Epub 2019 Jul 24.
6
What features of the built environment matter most for mobility? Using wearable sensors to capture real-time outdoor environment demand on gait performance.建成环境的哪些特征对出行最为重要?利用可穿戴传感器捕捉户外实时环境对步态表现的要求。
Gait Posture. 2019 Feb;68:437-442. doi: 10.1016/j.gaitpost.2018.12.028. Epub 2018 Dec 20.
7
Walking and weakness in children: a narrative review of gait and functional ambulation in paediatric neuromuscular disease.儿童行走和无力:儿科神经肌肉疾病步态和功能性步行的叙述性综述。
J Foot Ankle Res. 2020 Mar 2;13(1):10. doi: 10.1186/s13047-020-0378-2.
8
Are mice good models for human neuromuscular disease? Comparing muscle excursions in walking between mice and humans.老鼠是否适合作为人类神经肌肉疾病的模型?比较小鼠和人类行走时的肌肉运动。
Skelet Muscle. 2017 Nov 16;7(1):26. doi: 10.1186/s13395-017-0143-9.
9
Noninvasive and quantitative evaluation of movement disorder disability using an infrared depth sensor.利用红外深度传感器对运动障碍残疾进行无创和定量评估。
J Clin Neurosci. 2020 Jan;71:135-140. doi: 10.1016/j.jocn.2019.08.101. Epub 2019 Sep 26.
10
Concurrent validity and reliability of a low-cost gait analysis system for assessment of spatiotemporal gait parameters.低成本步态分析系统评估时空步态参数的同时效度和信度。
J Rehabil Med. 2019 Jun 18;51(6):456-463. doi: 10.2340/16501977-2559.

引用本文的文献

1
Jun N-Terminal Kinase Inhibitor Suppresses CASK Deficiency-Induced Cerebellar Granular Cell Death in MICPCH Syndrome Model Mice.Jun N端激酶抑制剂可抑制MICPCH综合征模型小鼠中CASK缺乏诱导的小脑颗粒细胞死亡。
Cells. 2025 May 20;14(10):750. doi: 10.3390/cells14100750.
2
Injectable sustainable andrographolide-releasing hydrogel for long-lasting alleviation of osteoarthritis and regulation of chondrocyte autophagy via PRKCA/EGFR.可注射的可持续释放穿心莲内酯水凝胶,用于通过蛋白激酶Cα/表皮生长因子受体实现骨关节炎的长期缓解和软骨细胞自噬的调控。
Mater Today Bio. 2025 Feb 25;31:101610. doi: 10.1016/j.mtbio.2025.101610. eCollection 2025 Apr.
3
Robust behavioral assessment of the inducible Friedreich's ataxia mouse does not show improvement with NRF2 induction.对诱导型弗里德赖希共济失调小鼠进行的强有力行为评估未显示出NRF2诱导后有改善。
Dis Model Mech. 2025 Mar 1;18(3). doi: 10.1242/dmm.052128. Epub 2025 Apr 2.
4
aux orchestrates the phosphorylation-dependent assembly of the lysosomal V-ATPase in glia and contributes to SNCA/α-synuclein degradation.辅助蛋白协调胶质细胞中溶酶体V-ATP酶的磷酸化依赖性组装,并促进α-突触核蛋白(SNCA/α-synuclein)的降解。
Autophagy. 2025 May;21(5):1039-1058. doi: 10.1080/15548627.2024.2442858. Epub 2025 Jan 29.
5
Discovery of Glucose Metabolism-Associated Genes in Neuropathic Pain: Insights from Bioinformatics.神经性疼痛中葡萄糖代谢相关基因的发现:来自生物信息学的见解
Int J Mol Sci. 2024 Dec 17;25(24):13503. doi: 10.3390/ijms252413503.
6
Compound Probiotics Improve Neuropathic Pain Prognosis in a Murine Model of Chronic Constriction Injury.复合益生菌改善慢性缩窄性损伤小鼠模型中的神经性疼痛预后。
J Pain Res. 2024 Dec 11;17:4213-4221. doi: 10.2147/JPR.S486259. eCollection 2024.
7
1,4-dihydroxy-2-naphthoic acid prevents 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine-induced motor function deficits.1,4 - 二羟基 - 2 - 萘甲酸可预防1 - 甲基 - 4 - 苯基 - 1,2,3,6 - 四氢吡啶诱导的运动功能缺陷。
Behav Pharmacol. 2025 Feb 1;36(1):40-46. doi: 10.1097/FBP.0000000000000806. Epub 2024 Dec 12.
8
Behavioral decline in Shank3 mice during early adulthood parallels cerebellar granule cell glutamatergic synaptic changes.成年早期Shank3基因敲除小鼠的行为衰退与小脑颗粒细胞谷氨酸能突触变化平行。
Mol Autism. 2024 Dec 4;15(1):52. doi: 10.1186/s13229-024-00628-y.
9
CatWalk XT Gait Parameters Associated with Mouse Achilles Tendon Injury and Healing.与小鼠跟腱损伤和愈合相关的CatWalk XT步态参数
Muscles Ligaments Tendons J. 2024 Apr-Jun;14(2):376-385. doi: 10.32098/mltj.02.2024.19.
10
Sucla2 Knock-Out in Skeletal Muscle Yields Mouse Model of Mitochondrial Myopathy With Muscle Type-Specific Phenotypes.骨骼肌中Sucla2基因敲除产生具有肌肉类型特异性表型的线粒体肌病小鼠模型。
J Cachexia Sarcopenia Muscle. 2024 Dec;15(6):2729-2742. doi: 10.1002/jcsm.13617. Epub 2024 Oct 31.

本文引用的文献

1
Low-cost Protocol of Footprint Analysis and Hanging Box Test for Mice Applied the Chronic Restraint Stress.应用慢性束缚应激的小鼠足迹分析与悬挂箱试验低成本方案
J Vis Exp. 2019 Jan 23(143). doi: 10.3791/59027.
2
Trendelenburg-Like Gait, Instability and Altered Step Patterns in a Mouse Model for Limb Girdle Muscular Dystrophy 2i.肢带型肌营养不良2i小鼠模型中的类Trendelenburg步态、不稳定性及步幅模式改变
PLoS One. 2016 Sep 14;11(9):e0161984. doi: 10.1371/journal.pone.0161984. eCollection 2016.
3
Gait analysis methods for rodent models of arthritic disorders: reviews and recommendations.关节炎疾病啮齿动物模型的步态分析方法:综述与建议。
Osteoarthritis Cartilage. 2016 Nov;24(11):1837-1849. doi: 10.1016/j.joca.2016.03.008. Epub 2016 Mar 17.
4
Quantification of gait parameters in freely walking rodents.自由行走啮齿动物步态参数的量化
BMC Biol. 2015 Jul 22;13:50. doi: 10.1186/s12915-015-0154-0.
5
Policy: NIH to balance sex in cell and animal studies.政策:NIH 将在细胞和动物研究中平衡性别。
Nature. 2014 May 15;509(7500):282-3. doi: 10.1038/509282a.
6
Muscle expression of mutant androgen receptor accounts for systemic and motor neuron disease phenotypes in spinal and bulbar muscular atrophy.肌萎缩性脊髓侧索硬化症和延髓性肌肉萎缩症中,突变雄激素受体的肌肉表达导致全身性和运动神经元疾病表型。
Neuron. 2014 Apr 16;82(2):295-307. doi: 10.1016/j.neuron.2014.03.001.
7
Identification methods in newborn C57BL/6 mice: a developmental and behavioural evaluation.新生 C57BL/6 小鼠的鉴定方法:发育和行为评估。
Lab Anim. 2010 Apr;44(2):88-103. doi: 10.1258/la.2009.009044. Epub 2009 Oct 23.
8
The detection and measurement of locomotor deficits in a transgenic mouse model of Huntington's disease are task- and protocol-dependent: influence of non-motor factors on locomotor function.在亨廷顿舞蹈症转基因小鼠模型中,运动功能缺陷的检测与测量取决于任务和实验方案:非运动因素对运动功能的影响。
Brain Res Bull. 2009 Mar 30;78(6):347-55. doi: 10.1016/j.brainresbull.2008.10.007. Epub 2008 Nov 14.
9
Treadmill gait analysis does not detect motor deficits in animal models of Parkinson's disease or amyotrophic lateral sclerosis.跑步机步态分析无法检测帕金森病或肌萎缩侧索硬化症动物模型中的运动缺陷。
J Mot Behav. 2008 Nov;40(6):568-77. doi: 10.3200/JMBR.40.6.568-577.
10
Motor coordination and balance in rodents.啮齿动物的运动协调与平衡
Curr Protoc Neurosci. 2001 Aug;Chapter 8:Unit 8.12. doi: 10.1002/0471142301.ns0812s15.