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2017 Fiscal Year Final Research Report

Identification of neurotoxic Abeta oligomers and development of therapy against them

Research Project

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Project/Area Number 15K09305
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Research Field Neurology
Research InstitutionHirosaki University

Principal Investigator

Kawarabayashi Takeshi  弘前大学, 医学研究科, 准教授 (90186156)

Co-Investigator(Renkei-kenkyūsha) SHOJI Mikio  弘前大学, 大学院医学研究科, 教授 (60171021)
NAKAMURA Takumi  弘前大学, 医学部附属病院, 助教 (80744193)
Project Period (FY) 2015-04-01 – 2018-03-31
KeywordsAbeta oligomer / Alzheimer's disease / tau / lipid rafts / vaccine
Outline of Final Research Achievements

Abeta dimers were accumulated in synaptic lipid rafts with increased fyn, phosphorylated NMDA receptors and phosphorylated tau in Alzheimer’s disease (AD) model mice. Abeta dimers could be neurotoxic Abeta to induce fyn/NMDA cascade and phosphorylated tau.
We generated a novel transgenic plant-based vaccine, a soybean storage protein containing Abeta4-10, named Abeta+. Abeta+ was administered orally to AD model mice. Spatial learning deterioration was prevented. Soluble Abeta oligomers were decreased. Abeta deposition and microgliosis was inhibited. Decrease of soluble Abeta oligomers by our vaccine could be a promising therapy for AD.

Free Research Field

神経内科

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Published: 2019-03-29  

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