Development of New Therapeutic Strategies for Animal Models of Retinal Degeneration by chitin and chitosan.
Project/Area Number |
25462740
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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 |
Ophthalmology
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Research Institution | Kansai Medical University |
Principal Investigator |
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Co-Investigator(Kenkyū-buntansha) |
TSUBURA Airo 関西医科大学, 医学部, 教授 (90098137)
YURI Takashi 関西医科大学, 医学部, 講師 (50330212)
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Project Period (FY) |
2013-04-01 – 2016-03-31
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Project Status |
Completed (Fiscal Year 2015)
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Budget Amount *help |
¥5,070,000 (Direct Cost: ¥3,900,000、Indirect Cost: ¥1,170,000)
Fiscal Year 2015: ¥650,000 (Direct Cost: ¥500,000、Indirect Cost: ¥150,000)
Fiscal Year 2014: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Fiscal Year 2013: ¥2,860,000 (Direct Cost: ¥2,200,000、Indirect Cost: ¥660,000)
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Keywords | 網膜色素変性症 / 視細胞 / 緑茶抽出物 / クルクミン / 酸化ストレス / MNU / 動物モデル / 併用効果 / エピガロカテキンガレート / MNU |
Outline of Final Research Achievements |
The purpose of the present study was to evaluate the efficacy of curcumin (CUR) and green tea extracts (GTE) as antioxidants against MNU-induced photoreceptor apoptosis. Furthermore, combinational effects were evaluated. Seven-week-old female Sprague-Dawley rats received a single intraperitoneal administration of 40 mg/kg MNU. Intraperitoneal administration of 200mg/kg CUR or oral administration of 250mg/kg GTE started 3 days prior to MNU exposure, and the administration was continued once daily for 10 days. Both CUR and GTE inhibited MNU-induced photoreceptor cell apoptosis by suppressing oxidative stress as seen by oxidative makers. These findings indicate that CUR and GTE may help to suppress the onset and progression of human RP. However, we could not confirm additive action and/or synergistic effect by CUR and GTE.
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Report
(4 results)
Research Products
(12 results)
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[Presentation] 緑茶抽出物によるラット肝臓毒性.2014
Author(s)
義澤克彦, 榎本祐子, 木下勇一, 圦 貴司, 結城美智子, 吉川 豊, 茶山和敏, 螺良愛郎.
Organizer
第103回日本病理学会
Place of Presentation
広島(広島国際会議場)
Year and Date
2014-04-25
Related Report
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