P-15 New hericenones including a protective agent against ER stress-dependent Neuro2a cell death from the medicinal mushroom of Hericium erinaceum(Poster Presentation)
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- Ueda Keiko
- Graduate School of Science and Technology, Shizuoka University
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- Tsujimori Megumi
- Faculty of Agriculture, Shizuoka University
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- Kodani Shinya
- Graduate School of Science and Technology, Shizuoka University:Faculty of Agriculture, Shizuoka University
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- Chiba Akiko
- Faculty of Agriculture, Shizuoka University
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- Masuno Kazuhiko
- Nagano Prefecture General Forest Research Center
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- Kubo Masakazu
- Kubo Industry Co., Ltd
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- Nagai Kaoru
- Graduate School of Medicine and Engineering, University of Yamanashi
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- Sekiya Atsushi
- Forestry and Forest Products Research Institute
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- Kawagishi Hirokazu
- Graduate School of Science and Technology, Shizuoka University:Faculty of Agriculture, Shizuoka University
Bibliographic Information
- Other Title
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- P-15 ヤマブシタケ(Hericium erinaceum)から得られた小胞体ストレスによる細胞死阻害物質(ポスター発表の部)
Description
The importance of the endoplasmic reticulum (ER) in triggering a specific program of cell death has been recently reported. By triggering apoptosis on neural cells, ER-stress is a major cause of neurodegenerating disease such as Alzheimer disease. The demand for new protective substances to the ER-stress-dependent cell death prompted us to screen the protective activity of mushrooms. On the course of the screening, we isolated new hericenones, 3-hydroxy-hericenone F as a protective agent, along with related compounds, hericenone I and J. The structures of hericenones were determined by NMR and MS spectra. The structure of 3-hydroxy hericenone was elucidated as (8-formyl-3-hydroxy-5-methoxy-2-methyl-2-(4'-methyl-2'-oxopent-3'-enyl) chroman-7-yl) methyl palmitate, which had one additional hydroxy group compared to hericenone F. 3-Hydroxy-hericenone F showed the protective activity dose-dependently, however hericenones F, I and J did not have any activity at the concentration of 10μg/mL. Therefore, we suggested that the hydroxy group of 3-hydroxy-hericenone F was important for the protective activity. This is the first report of a new hericenone which has the protective activity against ER stress-dependent cell death. The further study using more hericenones is needed for the understanding of the structure-activity relationship.
Journal
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- Symposium on the Chemistry of Natural Products, symposium papers
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Symposium on the Chemistry of Natural Products, symposium papers 50 (0), 309-314, 2008
Symposium on the Chemistry of Natural Products Steering Committee
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Details 詳細情報について
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- CRID
- 1390282681055336576
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- NII Article ID
- 110007066744
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- ISSN
- 24331856
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- Text Lang
- ja
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- Data Source
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- JaLC
- CiNii Articles
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- Abstract License Flag
- Disallowed