Behavioral Phenotype in the TgF344-AD Rat Model of Alzheimer's Disease

被引:34
|
作者
Sare, Rachel Michelle [1 ]
Cooke, Spencer K. [1 ]
Krych, Leland [1 ]
Zerfas, Patricia M. [2 ]
Cohen, Robert M. [3 ]
Smith, Carolyn Beebe [1 ]
机构
[1] NIMH, Sect Neuroadaptat & Prot Metab, NIH, Dept Hlth & Human Serv, Bethesda, MD 20892 USA
[2] NIH, Diagnost & Res Serv, Off Res Serv, Dept Hlth & Human Serv, Bethesda, MD USA
[3] Emory Univ, Sch Med, Dept Psychiat & Behav Sci, Atlanta, GA USA
关键词
Alzheimer's disease; amybid-beta; actigraphy; hyposmia; learning; BETA;
D O I
10.3389/fnins.2020.00601
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Alzheimer's disease (AD) is a progressive neurodegenerative disease resulting in cognitive decline. A unique rat model, TgF344-AD, recapitulates pathological hallmarks of AD. We used a longitudinal design to address the timing of expression of behavioral phenotypes in male and female TgF344-AD rats. In both sexes, we confirmed an age-dependent buildup of amyloid-beta. In the open field, female, but not male, TgF344-AD rats were hypoactive at 6 and 12 months of age but at 18 months the two genotypes were similar in levels of activity response. Both male and female TgF344-AD rats had a deficit in performance on a learning and memory task. Male TgF344-AD, but not female, rats had evidence of hyposmia regardless of age. Rest-activity rhythms followed the typical active/inactive phase in all rats regardless of genotype or age. In males, home cage activity was similar across age and genotype; in females, regardless of genotype animals were less active as they aged. These changes highlight some behavioral markers of disease in the rat model. Early markers of disease may be important in early diagnosis and assessment of efficacy when treatment becomes available.
引用
收藏
页数:10
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