1. The protective role of endogenous n-3 polyunsaturated fatty acids in Tau Alzheimer's disease mouse model
- Author
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Guang Fang, Baoyan Shi, Ren Huang, Jing xuan Kang, Sa Xiao, Xiang Gao, Chen Siyu, Li Wende, and Kefeng Wu
- Subjects
0301 basic medicine ,Genetically modified mouse ,Fatty Acid Desaturases ,Male ,medicine.medical_specialty ,genetic structures ,Amyloid ,Tau protein ,Endogeny ,Mice, Transgenic ,tau Proteins ,Disease ,03 medical and health sciences ,Mice ,0302 clinical medicine ,Alzheimer Disease ,Internal medicine ,Fatty Acids, Omega-3 ,medicine ,Animals ,Humans ,Maze Learning ,N 3 pufa ,chemistry.chemical_classification ,biology ,Behavior, Animal ,General Neuroscience ,food and beverages ,Brain ,General Medicine ,Neuroprotection ,Mice, Inbred C57BL ,Disease Models, Animal ,030104 developmental biology ,Endocrinology ,chemistry ,Docosahexaenoic acid ,biology.protein ,lipids (amino acids, peptides, and proteins) ,Female ,030217 neurology & neurosurgery ,Polyunsaturated fatty acid - Abstract
The role of n-3 polyunsaturated fatty acid (PUFA) as the main docosahexaenoic acid (DHA) in Alzheimer's disease (AD) remains controversial. Our study aimed to provide detailed information about the role of endogenous n-3 PUFAs in AD.Here, we generated a fat-1/tau transgenic mouse AD model by crossing female tau mice with male fat-1 mice to exclude confounding variables associated with the benefit of a DHA diet in these AD mice models. PUFAs presented in these AD models were detected by gas chromatography, and the role of endogenous n-3 PUFAs was assessed by lifespan survival assay, behavioral, pathologic, and molecular biology testing as well as imaging of cerebral vasculature.Endogenous n-3 PUFAs were shown to improve the memory and learning ability of AD mice. One possible reason for this improvement is the reduced formation of neurotrophic factors (NFTs) and Aβ amyloid plaques which usually damage hippocampal neurons. Additionally, endogenous n-3 PUFAs were demonstrated to protect cerebral vascular of AD mice, thereby increasing brain metabolism. Besides, endogenous n-3 PUFAs were observed to extend of the overall survival of tau mouse models.Endogenous n-3 PUFAs delayed the onset of Alzheimer's disease caused by tau protein dysfunction, alleviating related symptoms and significantly prolonging survival in vivo.
- Published
- 2018