Abnormal whisker movements in the 3xTg-AD mouse model of Alzheimer's disease

IF 2.4 4区 心理学 Q2 BEHAVIORAL SCIENCES
Ugne Simanaviciute, Richard E. Brown, Aimee Wong, Emre Fertan, Robyn A. Grant
{"title":"Abnormal whisker movements in the 3xTg-AD mouse model of Alzheimer's disease","authors":"Ugne Simanaviciute,&nbsp;Richard E. Brown,&nbsp;Aimee Wong,&nbsp;Emre Fertan,&nbsp;Robyn A. Grant","doi":"10.1111/gbb.12813","DOIUrl":null,"url":null,"abstract":"<p>Alzheimer's disease is the most frequent form of dementia in elderly people. The triple transgenic (3xTg-AD) mouse model of Alzheimer's Disease is important in biomedical research as these mice develop both neuropathological and behavioural phenotypes. However, their behavioural phenotype is variable, with findings depending on the specific task, as well as the age and sex of the mice. Whisker movements show motor, sensory and cognitive deficits in mouse models of neurodegenerative disease. Therefore, we examined whisker movements in 3, 12.5 and 17-month-old female 3xTg-AD mice and their B6129S/F2 wildtype controls. Mice were filmed using a high-speed video camera (500 fps) in an open arena during a novel object exploration task. Genotype and age differences were found in mice exploring the arena prior to object contact. Prior to whisker contact, the 3-month-old 3xTg-AD mice had smaller whisker angles compared with the wildtype controls, suggesting an early motor phenotype in these mice. Pre-contact mean angular position at 3 months and whisking amplitude at 17 months of age differed between the 3xTg-AD and wildtype mice. During object contact 3xTg-AD mice did not reduce whisker spread as frequently as the wildtype mice at 12.5 and 17 months, which may suggest sensory or attentional deficits. We show that whisker movements are a powerful behavioural measurement tool for capturing behavioural deficits in mouse models that show complex phenotypes, such as the 3xTg-AD mouse model.</p>","PeriodicalId":50426,"journal":{"name":"Genes Brain and Behavior","volume":"21 8","pages":""},"PeriodicalIF":2.4000,"publicationDate":"2022-06-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/48/a4/GBB-21-e12813.PMC9744487.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Genes Brain and Behavior","FirstCategoryId":"102","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1111/gbb.12813","RegionNum":4,"RegionCategory":"心理学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BEHAVIORAL SCIENCES","Score":null,"Total":0}
引用次数: 0

Abstract

Alzheimer's disease is the most frequent form of dementia in elderly people. The triple transgenic (3xTg-AD) mouse model of Alzheimer's Disease is important in biomedical research as these mice develop both neuropathological and behavioural phenotypes. However, their behavioural phenotype is variable, with findings depending on the specific task, as well as the age and sex of the mice. Whisker movements show motor, sensory and cognitive deficits in mouse models of neurodegenerative disease. Therefore, we examined whisker movements in 3, 12.5 and 17-month-old female 3xTg-AD mice and their B6129S/F2 wildtype controls. Mice were filmed using a high-speed video camera (500 fps) in an open arena during a novel object exploration task. Genotype and age differences were found in mice exploring the arena prior to object contact. Prior to whisker contact, the 3-month-old 3xTg-AD mice had smaller whisker angles compared with the wildtype controls, suggesting an early motor phenotype in these mice. Pre-contact mean angular position at 3 months and whisking amplitude at 17 months of age differed between the 3xTg-AD and wildtype mice. During object contact 3xTg-AD mice did not reduce whisker spread as frequently as the wildtype mice at 12.5 and 17 months, which may suggest sensory or attentional deficits. We show that whisker movements are a powerful behavioural measurement tool for capturing behavioural deficits in mouse models that show complex phenotypes, such as the 3xTg-AD mouse model.

Abstract Image

Abstract Image

Abstract Image

Abstract Image

阿尔茨海默病3xTg-AD小鼠模型的异常须运动
阿尔茨海默病是老年人中最常见的痴呆症。三重转基因(3xTg-AD)阿尔茨海默病小鼠模型在生物医学研究中具有重要意义,因为这些小鼠具有神经病理和行为表型。然而,它们的行为表型是可变的,其结果取决于特定的任务,以及小鼠的年龄和性别。在神经退行性疾病的小鼠模型中,须运动显示出运动、感觉和认知缺陷。因此,我们检测了3、12.5和17月龄雌性3xTg-AD小鼠及其B6129S/F2野生型对照的须运动。研究人员用高速摄像机(500帧/秒)拍摄了老鼠在一个开放的舞台上进行新物体探索任务的过程。在接触物体之前探索竞技场的小鼠中发现了基因型和年龄差异。在触须接触之前,与野生型对照相比,3个月大的3xTg-AD小鼠的触须角度更小,这表明这些小鼠存在早期运动表型。3xTg-AD小鼠与野生型小鼠在接触前3月龄的平均角位置和17月龄的摆动幅度存在差异。在12.5个月和17个月时,3xTg-AD小鼠在接触物体时,胡须扩散的频率不如野生型小鼠,这可能表明感觉或注意力缺陷。我们发现,在表现出复杂表型的小鼠模型(如3xTg-AD小鼠模型)中,须运动是捕获行为缺陷的强大行为测量工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Genes Brain and Behavior
Genes Brain and Behavior 医学-行为科学
CiteScore
6.80
自引率
4.00%
发文量
62
审稿时长
4-8 weeks
期刊介绍: Genes, Brain and Behavior was launched in 2002 with the aim of publishing top quality research in behavioral and neural genetics in their broadest sense. The emphasis is on the analysis of the behavioral and neural phenotypes under consideration, the unifying theme being the genetic approach as a tool to increase our understanding of these phenotypes. Genes Brain and Behavior is pleased to offer the following features: 8 issues per year online submissions with first editorial decisions within 3-4 weeks and fast publication at Wiley-Blackwells High visibility through its coverage by PubMed/Medline, Current Contents and other major abstracting and indexing services Inclusion in the Wiley-Blackwell consortial license, extending readership to thousands of international libraries and institutions A large and varied editorial board comprising of international specialists.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信