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2019 Fiscal Year Final Research Report

recording and analysis of neuronal oscillation in humans

Planned Research

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Project AreaNon-linear Neuro-oscillology: Towards Integrative Understanding of Human Nature
Project/Area Number 15H05874
Research Category

Grant-in-Aid for Scientific Research on Innovative Areas (Research in a proposed research area)

Allocation TypeSingle-year Grants
Review Section Complex systems
Research InstitutionKyoto University

Principal Investigator

Ikeda Akio  京都大学, 医学研究科, 特定教授 (90212761)

Co-Investigator(Kenkyū-buntansha) 松本 理器  神戸大学, 医学研究科, 教授 (00378754)
長峯 隆  札幌医科大学, 医学部, 教授 (10231490)
菊池 隆幸  京都大学, 医学研究科, 助教 (40625084)
小林 勝弘  岡山大学, 医歯薬学総合研究科, 教授 (60273984)
國枝 武治  愛媛大学, 医学系研究科, 教授 (60609931)
宇佐美 清英  京都大学, 医学研究科, 特定助教 (20829204)
Project Period (FY) 2015-06-29 – 2020-03-31
KeywordsActive DC shifts / Red slow
Outline of Final Research Achievements

We developed the concept of "Active DC shifts" as the Electrocorticogram(ECoG) biomarker of epileptic focus through the application of mathematical model on ECoG, multi-institutional analysis of surgical specimen, or animal model. We revealed the importance of neuron and glial cells in epileptic seizure generation. We clarified that the "red slow", the co-occurrence of slow wave and high frequency oscillation, was observed in the same areas where active DC shifts were recorded. On the other hand, we showed the versatility of these biomarker (active DC shifts and red slow) for the scalp-recorded electroencephalogram.

Free Research Field

てんかん学、神経生理学

Academic Significance and Societal Importance of the Research Achievements

本研究で明らかにされたActive ictal DC shiftsやRed slowなどの新規のてんかん焦点の生理バイオマーカーを臨床に応用することで、難治てんかん患者に対するてんかん焦点切除術に際して、術前のてんかん焦点同定に役立ち、手術成績の向上に寄与しうる。また、本研究を通じ明らかにされたグリア細胞のてんかん発作における重要性から、グリア細胞が今後の抗てんかん薬の創薬のターゲットになりうることが示された。

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Published: 2021-02-19  

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