Elucidation of molecular/neural mechanisms for memory extinction by inducible and reversible gene expression
Project/Area Number |
24590133
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Research Category |
Grant-in-Aid for Scientific Research (C)
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Allocation Type | Multi-year Fund |
Section | 一般 |
Research Field |
Biological pharmacy
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Research Institution | Tokushima Bunri University |
Principal Investigator |
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Project Period (FY) |
2012-04-01 – 2015-03-31
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Project Status |
Completed (Fiscal Year 2014)
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Budget Amount *help |
¥5,200,000 (Direct Cost: ¥4,000,000、Indirect Cost: ¥1,200,000)
Fiscal Year 2014: ¥780,000 (Direct Cost: ¥600,000、Indirect Cost: ¥180,000)
Fiscal Year 2013: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Fiscal Year 2012: ¥2,860,000 (Direct Cost: ¥2,200,000、Indirect Cost: ¥660,000)
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Keywords | 瞬目反射条件づけ / 消去 / 内在性カンナビノイド / 代謝型グルタミン酸受容体 / 運動学習 / アルツハイマー病 / プリオン / 加齢発達 / カンナビノイド受容体 / 2-AG / 空間学習 / 潜在学習 / 恐怖記憶 / 瞬目反射条件付け / 記憶学習 / 加齢 / 忘却 / 遺伝子改変動物 / 発達 / 実験的消去 / 小脳学習 / 遺伝子改変マウス |
Outline of Final Research Achievements |
The neural mechanisms of memory extinction were investigated by using pharmacological analysis and various mouse models (inducible and reversible KO mice, Alzheimer's disease (AD) model mice, prion protein KO mice, KO mice of monoacylglycerol lipase (MGL), the major hydrolyzing enzyme of 2-AG, and so on). The main results obtained in the study are summarized in the following points: (i) To determine the sites for extinction of eyeblink memory in the cerebellum, we used mGluR1-conditional KO mice bearing inducible and reversible expression of mGluR1 specifically in cerebellar Purkinje cells (PCs). We found that extinction of eyeblink memory was slightly impaired without mGluR1 in PCs. (ii) MGL KO mice showed impaired extinction of eyeblink memory, though fatty acid amide hydrolase (FAAH) inhibition significantly impaired memory acquisition. (iii) In the AD model mice, the impairment of trace memory acquisition preceded impairment of the memory extinction.
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Report
(4 results)
Research Products
(25 results)
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[Journal Article] The synaptic targeting of mGluR1 by its carboxyl-terminal domain Is crucial for cerebellar function2014
Author(s)
Yoshiaki Ohtani, Mariko Miyata, Kouichi Hashimoto, Toshihide Tabata, Yasushi Kishimoto, Masahiro Fukaya, Daisuke Kase, Hidetoshi Kassai, Kazuki Nakao, Tatsumi Hirata, Masahiko Watanabe, Masanobu Kano, Atsu Aiba
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Journal Title
Journal of Neuroscience
Volume: 34
Issue: 7
Pages: 2702-2712
DOI
Related Report
Peer Reviewed
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