The TgF344-AD rat: behavioral and proteomic changes associated with aging and protein expression in a transgenic rat model of Alzheimer's disease

被引:11
|
作者
Bac, Birsu [1 ]
Hicheri, Cheima [1 ]
Weiss, Craig [1 ]
Buell, Amelia [1 ]
Vilcek, Natalia [1 ]
Spaeni, Claudia [1 ]
Geula, Changiz [2 ]
Savas, Jeffrey N. [3 ]
Disterhoft, John F. [1 ]
机构
[1] Northwestern Univ, Feinberg Sch Med, Dept Neurosci, Chicago, IL 60611 USA
[2] Northwestern Univ, Mesulam Ctr Cognit Neurol & Alzheimers Dis, Feinberg Sch Med, Chicago, IL USA
[3] Northwestern Univ, Feinberg Sch Med, Dept Neurol, Chicago, IL USA
关键词
Watermaze; pTau; Neuroinflammation; TREM2; Learning index; Proteomics; HIPPOCAMPAL CA1 NEURONS; COGNITIVE IMPAIRMENT; CEREBROSPINAL-FLUID; LEARNING-ABILITY; SEX-DIFFERENCES; A-BETA; TAU; EXCITABILITY; MEMORY; NEUROPATHOLOGY;
D O I
10.1016/j.neurobiolaging.2022.12.015
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Animal models of Alzheimer's Disease (AD) are attractive tools for preclinical, prodromal drug testing. The TgF344-AD (Tg) rat exhibits cognitive deficits and 5 major hallmarks of AD. Here we show that spatial water maze (WMZ) memory deficits and proteomic differences in dorsal CA1 were present in young Tg rats. Aged learning-unimpaired (AU) and aged learning-impaired (AI) proteome associated changes were identified and differed by sex. Levels of phosphorylated tau, reactive astrocytes and microglia were signif-icantly increased in aged Tg rats and correlated with the WMZ learning index (LI); in contrast, no signifi-cant correlation was present between amyloid plaques or insoluble A,B levels and LI. Neuroinflammatory markers were also significantly correlated with LI and increased in female Tg rats. The anti-inflammatory marker, triggering receptor expressed on myeloid cells-2 (TREM2), was significantly reduced in aged im-paired Tg rats and correlated with LI. Identifying and understanding mechanisms that allow for healthy aging by overcoming genetic drivers for AD, and/or promoting drivers for successful aging, are important for developing successful therapeutics against AD.(c) 2022 The Author(s). Published by Elsevier Inc.his is an open access article under the CC BY-NC-ND license ( http://creativecommons.org/licenses/by-nc-nd/4.0/ )
引用
收藏
页码:98 / 110
页数:13
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