Sex Dimorphism Profile of Alzheimer's Disease-Type Pathologies in an APP/PS1 Mouse Model

被引:89
|
作者
Jiao, Shu-Sheng [1 ]
Bu, Xian-Le [1 ]
Liu, Yu-Hui [1 ]
Zhu, Chi [1 ]
Wang, Qing-Hua [1 ]
Shen, Lin-Lin [1 ]
Liu, Cheng-Hui [1 ]
Wang, Ye-Ran [1 ]
Yao, Xiu-Qing [1 ]
Wang, Yan-Jiang [1 ]
机构
[1] Third Mil Med Univ, Daping Hosp, Dept Neurol, Chongqing, Peoples R China
基金
中国国家自然科学基金;
关键词
Alzheimer's disease; Sex dimorphism; Beta-amyloid; Cerebral amyloid angiopathy; Tau pathology; Neuroinflammation; Loss of neurons and synapses; HORMONE REPLACEMENT THERAPY; CEREBRAL AMYLOID ANGIOPATHY; GENDER-DIFFERENCES; TRANSGENIC MICE; OLDER WOMEN; BETA; DEMENTIA; ESTROGEN; PROTEINS; TAU;
D O I
10.1007/s12640-015-9589-x
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Alzheimer's disease (AD) is the most common form of dementia among the elderly, characterized by parenchymal and vascular beta-amyloid (A beta) burden, tau pathology, neuroinflammation, and loss of neurons and synapses. There is a clear sex difference in the prevalence of AD. However, sex differences in AD-type pathologies have not been systematically documented. Applying 12-month-old female and male APP/PS1 mice as a model, we investigated the sex dimorphism in these major pathological indices. Compared with male APP/PS1 mice, the females exhibited higher parenchymal A beta burdens, with the sex difference in hippocampus being the most significant. Female APP/PS1 mice had more severe cerebral amyloid angiopathy and subsequent microhemorrhage. In addition, female APP/PS1 mice also showed higher levels of phosphorylated tau and proinflammatory cytokines, more severe astrocytosis and microgliosis, and greater neuronal and synaptic degenerations. The present study systematically described a sex dimorphism in AD-type pathologic indices, suggesting that gender should be taken into account in designing studies involving these pathological indices and when interpreting the relevant findings in those studies.
引用
收藏
页码:256 / 266
页数:11
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