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The protective effect of dietary eicosapentaenoic acid against impairment of spatial cognition learning ability in rats infused with amyloid β₍₁₋₄₀₎
- Hashimoto, Michio, Hossain, Shahdat, Tanabe, Yoko, Kawashima, Akiko, Harada, Tsuyoshi, Yano, Takashi, Mizuguchi, Kiyoshi, Shido, Osamu
- Journal of nutritional biochemistry 2009 v.20 no.12 pp. 965-973
- dietary fat, eicosapentaenoic acid, omega-3 fatty acids, cognition, rats, animal models, amyloidosis, Alzheimer disease, hippocampus, memory, consciousness, nutrition-genotype interaction, synaptic transmission, signal transduction, oxidative stress, reactive oxygen species, arachidonic acid, protective effect, dietary nutrient sources, fish oils
- Background: Amyloid β (Aβ) peptide (1-40) can cause cognitive impairment. Experimental design: We investigated whether dietary preadministration of eicosapentaenoic acid (EPA) is conducive to cognition learning ability and whether it protects against the impairment of learning ability in rats infused with Aβ peptide (1-40) into the cerebral ventricle. Results: Dietary EPA administered to rats for 12 weeks before the infusion of Aβ into the rat brain significantly decreased the number of reference memory errors (RMEs) and working memory errors (WMEs), suggesting that chronic administration of EPA improves cognition learning ability in rats. EPA preadministered to the Aβ-infused rats significantly reduced the increase in the number of RMEs and WMEs, with concurrent proportional increases in the levels of corticohippocampal EPA and docosahexaenoic acid (DHA) and in the DHA/arachidonic acid molar ratio. Decrease in oxidative stress in these tissues was evaluated by determining the reactive oxygen species and lipid peroxide levels. cDNA microarray analysis revealed that altered genes included those that control synaptic signal transduction, cell communication, membrane-related vesicular transport functions, and enzymes and several other proteins. Conclusion: The present study suggests that EPA, by acting as a precursor for DHA, ameliorates learning deficits associated with Alzheimer's disease and that these effects are modulated by the expression of proteins involved in neuronal plasticity.