2021 Fiscal Year Final Research Report
Neurobiological mechanisms of cerebellar macroneuroplasticity associated with learning
Project/Area Number |
19H03536
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Research Category |
Grant-in-Aid for Scientific Research (B)
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Allocation Type | Single-year Grants |
Section | 一般 |
Review Section |
Basic Section 51010:Basic brain sciences-related
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Research Institution | Kyoto University (2020-2021) National Center of Neurology and Psychiatry (2019) |
Principal Investigator |
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Co-Investigator(Kenkyū-buntansha) |
阿部 弘基 横浜市立大学, 医学部, 助教 (40737409)
阿部 十也 国立研究開発法人国立精神・神経医療研究センター, 脳病態統合イメージングセンター, 部長 (60588515)
星野 幹雄 国立研究開発法人国立精神・神経医療研究センター, 神経研究所 病態生化学研究部, 部長 (70301273)
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Project Period (FY) |
2019-04-01 – 2022-03-31
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Keywords | 学習 |
Outline of Final Research Achievements |
It is increasingly clearer that we are able to observe neuroplastic changes in the brain associated with experiences and learning. Indeed, we have used MRI and found neuroplastic changes in the cerebellum associated with programming learning in humans and with operant conditioning in rodents. Here we intended to combine histological methodology and AMPA PET to elucidate neurobiological mechanisms underlying cerebellar neuroplasticity associated with learning in rats. We obtained PET data from 8 rats before and after operant learning and a control condition. We also acquired specimen after second PET scanning from both learning and control groups. We have developed methodology for histological methodology to measure cerebellar gray matter areas. We also developed methodology to assess changes in AMPA ligand uptake before and after learning. The statistical analysis is still underway.
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Free Research Field |
神経科学
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Academic Significance and Societal Importance of the Research Achievements |
脳構造マクロ可塑性の背景となる分子メカニズムはほとんど解明されていない。今後の解析により学習を支える脳構造マクロ可塑性の分子メカニズムが明らかになれば、ギャップの大きい分子レベルの神経科学的知見とMRIなど神経回路レベルの神経科学的知見が連結する契機となる。また、この知見は、学習障害の病態解明、神経損傷回復からのリハビリテーションによる促進、学習を促進するための創薬など幅広い社会応用の道筋が開けると期待される。
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