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2019 Fiscal Year Final Research Report

Development of novel brain protection therapy by regulating intestinal flora for ischemic brain injury

Research Project

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Project/Area Number 17K09763
Research Category

Grant-in-Aid for Scientific Research (C)

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

Principal Investigator

Urabe Takao  順天堂大学, 医学(系)研究科(研究院), 教授 (60291663)

Project Period (FY) 2017-04-01 – 2020-03-31
Keywords腸内細菌叢 / 虚血性大脳白質損傷 / 酸化ストレス / 炎症 / 認知障害
Outline of Final Research Achievements

In the present study, it was revealed that LPS is effluxed into the blood due to disruption of intestinal barrier function due to dysbiosis in the pathophysiology of diabetes mellitus due to chronic cerebral ischemia, resulting in metabolic endotoxemia. In addition, lipopolysaccharide (LPS) in blood acts on toll like receptor 4 (TLR4) whose expression is increased in the brain due to disruption of blood-brain barrier function due to cerebral ischemia. Moreover, activated immunocompetent cells produce inflammatory cytokines, and progresses inflammatory response. We have proved that the development of inflammatory reaction derived from dysbiosis causes onset and development of brain white matter damage.

Free Research Field

神経内科学

Academic Significance and Societal Importance of the Research Achievements

本研究は、腸内細菌叢異常による炎症反応が虚血性脳損傷の進展に関与するメカニズムを明らかにした内容であり、学術的に意義のある成果である。
さらに、超高齢化を迎えている我が国において、脳梗塞発症のみならず認知症発症の病態に腸内細菌叢変化による炎症や酸化ストレスが関与することを示せたことは社会的にも意義が深いことである。

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Published: 2021-02-19  

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