| Project/Area Number |
26350981
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| Research Category |
Grant-in-Aid for Scientific Research (C)
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| Allocation Type | Multi-year Fund |
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| Section | 一般 |
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| Research Field |
Basic / Social brain science
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| Research Institution | Keio University |
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Principal Investigator |
Unekawa Miyuki 慶應義塾大学, 医学部(信濃町), 特任講師 (10548481)
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| 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)
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| 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)
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| Research Collaborator |
SUZUKI Norihiro
KANNO Iwao
WATANABE Tatsushi
HATAKEYAMA Nao
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| Project Period (FY) |
2014-04-01 – 2018-03-31
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| Project Status |
Completed (Fiscal Year 2017)
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| Budget Amount *help |
¥4,680,000 (Direct Cost: ¥3,600,000、Indirect Cost: ¥1,080,000)
Fiscal Year 2017: ¥910,000 (Direct Cost: ¥700,000、Indirect Cost: ¥210,000)
Fiscal Year 2016: ¥910,000 (Direct Cost: ¥700,000、Indirect Cost: ¥210,000)
Fiscal Year 2015: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Fiscal Year 2014: ¥1,300,000 (Direct Cost: ¥1,000,000、Indirect Cost: ¥300,000)
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| 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 / アストログリア / 赤血球速度 / グリア細胞 / neurovasucular unit |
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| 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.
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