Neural Regeneration Research ›› 2026, Vol. 21 ›› Issue (6): 2543-2552.doi: 10.4103/NRR.NRR-D-24-00975

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Lipidomic and sterolomic profiles of different brain regions in the mouse model of Alzheimer’s disease

Xingsen Zhao1, 2, #, Liqun Chen3, #, Liangjian Ma4, Xiaohui Liu5, Zhongkai Cao1, Xiangjun Chen6, *, Lidan Hu1, *   

  1. 1Department of Nephrology, The Children’s Hospital, Zhejiang University School of Medicine, National Clinical Research Center for Child Health, Hangzhou, Zhejiang Province, China; 
    2Institute of Biotechnology, Xianghu Laboratory, Hangzhou, Zhejiang Province, China; 
    3Academy of Medical Engineering and Translational Medicine, Medical College, Tianjin University, Tianjin, China; 
    4The First Clinical Medical College of Lanzhou University, Lanzhou, Gansu Province, China; 
    5Metabolomics and Lipidomics Center of Tsinghua University, Beijing, China; 
    6Institute of Translational Medicine, Zhejiang University School of Medicine, Hangzhou, Zhejiang Province, China
  • Online:2026-06-15 Published:2026-04-18
  • Contact: Lidan Hu, PhD, hulidan1@duke-nus.edu.sg; Xiangjun Chen, PhD, chenxiangjun@zju.edu.cn.
  • Supported by:
    This study was supported by the National Natural Science Foundation of China, Nos. 82200784, 32271311 and Qizhen Foundation, No. 226‐2023‐00008 (all to LH).

Abstract: 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.

Key words: Alzheimer’s disease, Alzheimer’s disease mouse model, brain lipids, dyslipidemias, lipidomic, metabolism, neurodegenerative disease, sterol