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2017 Fiscal Year Final Research Report

A role of astrocyte in neuro-glio-vascular unit concerning cerebral microcirculation

Research Project

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Project/Area Number 26350981
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Research Field Basic / Social brain science
Research InstitutionKeio University

Principal Investigator

Unekawa Miyuki  慶應義塾大学, 医学部(信濃町), 特任講師 (10548481)

Co-Investigator(Kenkyū-buntansha) 冨田 裕  慶應義塾大学, 医学部(信濃町), 講師(非常勤) (60276251)
Co-Investigator(Renkei-kenkyūsha) TANAKA Kenji  慶應義塾大学, 医学部, 准教授 (30329700)
MASAMOTO Kazuto  電気通信大学, 情報理工学部, 教授 (60455384)
Research Collaborator SUZUKI Norihiro  
KANNO Iwao  
WATANABE Tatsushi  
HATAKEYAMA Nao  
Project Period (FY) 2014-04-01 – 2018-03-31
Keywords光遺伝学 / 脳微小循環 / アストロサイト / ニューロン / neurovascular unit / 大脳皮質性拡延性抑制 / 脳梗塞 / Na-K-pump
Outline of Final Research Achievements

Photostimulation to transgenic mice expressing light-sensitive cation channel, channelrhodopsin-2, in astrocyte or neuron elicited intensity-dependent increase in cortical blood flow. Pharmacological study exhibited specific mechanism of astrocyte- or neuron-originated microcirculatory control.
Cortical spreading depression (CSD) involving mass depolarization of neuron and astrocyte elicited transient constriction and dilation of pial and intraparenchymal penetrating artery, followed by mild constriction, and deceleration of red blood cell (RBC) flowing in capillary in parallel with arterial constriction. Repeated CSD elicited marked dilation of penetrating artery and acceleration of RBC. Spontaneous occurrence of CSD during transient middle cerebral artery occlusion by modified Tamura's method may be involved in formation and/or development of infarction. Susceptibility to CSD was enhanced and recovery from CSD was elongated in familial hemiplegic migraine 2 model mice.

Free Research Field

神経生理学

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Published: 2019-03-29  

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