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Effect of Obesity and High-Density Lipoprotein Concentration on the Pathological Characteristics of Alzheimer's Disease in High-Fat Diet-Fed Miceopen accessEffect of Obesity and High-Density Lipoprotein Concentration on the Pathological Characteristics of Alzheimer's Disease in High-Fat Diet-Fed Mice

Other Titles
Effect of Obesity and High-Density Lipoprotein Concentration on the Pathological Characteristics of Alzheimer's Disease in High-Fat Diet-Fed Mice
Authors
Jeong, Yun HaChoi, Moon seokKim, Dong sooYoung Jin, YounJunghwa, Ryu
Issue Date
Oct-2022
Publisher
Multidisciplinary Digital Publishing Institute (MDPI)
Keywords
Alzheimer' s disease; high-fat diet; obesity; high-density lipoprotein; apolipoprotein AI; amyloid plaque
Citation
International Journal of Molecular Sciences, v.23, no.12296
Journal Title
International Journal of Molecular Sciences
Volume
23
Number
12296
URI
http://scholarworks.bwise.kr/kbri/handle/2023.sw.kbri/193
DOI
10.3390/ijms232012296
ISSN
1661-6596
Abstract
The typical pathological features of Alzheimer's disease (AD) are the accumulation of amyloid plaques in the brain and reactivity of glial cells such as astrocytes and microglia. Clinically, the development of AD and obesity are known to be correlated. In this study, we analyzed the changes in AD pathological characteristics in 5XFAD mice after obesity induction through a highfat diet (HFD). Surprisingly, high-density lipoprotein and apolipoprotein AI (APOA-I) serum levels were increased without low-density lipoprotein alteration in both HFD groups. The reactivity of astrocytes and microglia in the dentate gyrus of the hippocampus and fornix of the hypo-thalamus in 5XFAD mice was decreased in the transgenic (TG)-HFD high group. Finally, the accumulation of amyloid plaques in the dentate gyrus region of the hippocampus was also signifi-cantly decreased in the TG-HFD high group. These results suggest that increased high-density lipoprotein level, especially with increased APOA-I serum level, alleviates the pathological features of AD and could be a new potential therapeutic strategy for AD treatment.
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연구본부 (퇴행성뇌질환 연구그룹)
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