胰岛素降解酶
胰岛素抵抗
发病机制
内分泌学
内科学
疾病
淀粉样蛋白(真菌学)
认知
认知功能衰退
淀粉样前体蛋白分泌酶
淀粉样前体蛋白
神经科学
生物
阿尔茨海默病
医学
胰岛素
痴呆
病理
作者
Xiaokang Gong,Zheng Liang,Wei Liu,Yang Zhao,Youhua Yang,Mengjuan Wu,Jinting Shang,Yifan Xiao,Yong‐Mei Cha,Qiqi Su,Binlian Sun,Jian Bao,Xiji Shu
标识
DOI:10.2174/1567205018666210628100812
摘要
Alzheimer's disease (AD) is the most common neurodegenerative disorder and negative lifestyle factors may contribute to its etiopathogenesis. Substantial evidence from humans and murine models reveals that Insulin Resistance (IR) associated with a high fat diet (HFD) increases the risk of developing AD and age-related amyloidogenesis.The aim of the study was to corroborate and clarify the influence of HFD on amyloidogenesis and cognitive deficits in AD model mice.We here show that a four months HFD-feeding increases IR in both the periphery and brain of APP/PS1 mice, which are used as AD models. Meanwhile, long-term HFD exacerbates cognitive defects and impairs dendritic integrity and expressions of synaptic proteins in APP/PS1 mice. Furthermore, HFD induces an increase in β-secretase (BACE1) expression and a decrease in insulin-degrading enzyme (IDE) expression, resulting in β-amyloid (Aβ) accumulation.Our data suggest that long-term HFD, with the accompanying IR, promotes Aβ toxicity and cognitive deficits, indicating that modifiable lifestyle hazards such as HFD-induced IR might contribute to AD pathogenesis.
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