嗅球
早老素
脂质代谢
脂类学
生物
海马体
淀粉样前体蛋白
PSEN1型
甾醇
转基因小鼠
阿尔茨海默病
疾病
痴呆
神经科学
转基因
生物化学
基因
内科学
医学
胆固醇
中枢神经系统
作者
Xingsen Zhao,Long‐Qing Chen,Liangjian Ma,Xiaohui Liu,Zhongkai Cao,Xiangjun Chen,Lidan Hu
标识
DOI:10.4103/nrr.nrr-d-24-00975
摘要
JOURNAL/nrgr/04.03/01300535-202606000-00069/figure1/v/2026-02-11T151048Z/r/image-tiff Alzheimer's disease is the most common cause of dementia. Although increasing evidence suggests that disruptions in lipid metabolism are closely associated with the disease, the overall profile of lipid and sterol changes that occur in the brain during Alzheimer's disease remains unclear. In this study, we compared brain tissues extracted from 32-week-old male wild-type mice and 5×FAD transgenic Alzheimer's disease model mice, which carry mutations in the amyloid precursor protein ( APP ) and presenilin 1 ( PS1 ) genes. Using untargeted lipidomics and sterolomics techniques, we investigated the metabolic profiles of lipids, with a focus on sterols specifically, in three brain regions: cerebellum, hippocampus, and olfactory bulb. Our results revealed significant alterations in various lipids, particularly in the hippocampus and olfactory bulb, suggesting changes in energy levels in these regions. Further pathway analysis indicated notable disruptions in key metabolic processes, particularly those related to fatty acids and cell membrane components. Additionally, we observed decreased expression of 15 genes involved in lipid and sterol regulation. Collectively, these findings provide new insights into how imbalances in lipid and sterol metabolism may contribute to the progression of Alzheimer's disease, highlighting potential metabolic pathways involved in the development of this debilitating disease.
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