DNA and protein modification and disturbance on cell system with NO produced from photo-reactivation of N-nitrosated amino acids
| Project/Area Number |
20510064
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| Research Category |
Grant-in-Aid for Scientific Research (C)
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| Allocation Type | Single-year Grants |
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| Section | 一般 |
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| Research Field |
Risk sciences of radiation/Chemicals
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| Research Institution | Okayama University |
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Principal Investigator |
ARIMOTO Sakae 岡山大学, 大学院・医歯薬学総合研究科, 准教授 (90212654)
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| Co-Investigator(Kenkyū-buntansha) |
KIMURA Sachiko 兵庫県立大学, 環境人間学部, 助教 (70225035)
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| Project Period (FY) |
2008 – 2010
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| Project Status |
Completed (Fiscal Year 2010)
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| Budget Amount *help |
¥4,810,000 (Direct Cost: ¥3,700,000、Indirect Cost: ¥1,110,000)
Fiscal Year 2010: ¥910,000 (Direct Cost: ¥700,000、Indirect Cost: ¥210,000)
Fiscal Year 2009: ¥1,040,000 (Direct Cost: ¥800,000、Indirect Cost: ¥240,000)
Fiscal Year 2008: ¥2,860,000 (Direct Cost: ¥2,200,000、Indirect Cost: ¥660,000)
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| Keywords | ニトロソプロリン / DNA損傷 / 近紫外光 / 一酸化窒素 / アミノ酸修飾 / 光変異原性 / 光毒性 / ニトロソチロシン / DNA修飾 / 8-オキソデオキシグアノシン / デオキシイノシン / 光活性化 / デオキシオキザノシン / デオキシキサントシン |
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| Research Abstract |
The N-nitroso moiety of N-dialkylnitrosamines absorbs UVA photons, UVA-photolysis of N-dialkylnitrosamines brings release of nitric oxide, and subsequent production of alkyl radical cations and active oxygen species follow as secondary events, which cause DNA strand breaks, oxidative and alkylative DNA damages and mutation.
Photoproducts from NPRO and dA were isolated, analyzed by MS and NMR, and identified as deoxyinosine and(R)-,(S)-2-(2-pyrrolidyl)-2'-deoxyadenosine. When UV light of 365 nm was irradiated to a neutral mixture of N-nitrosoproline, gluthathione and tyrosine, S-nitrosoglutathione and 3-nitrotyrosine were generated. These results suggest that N-nitrosoproline may induce nitrosation and nitration of cellular components in humans with sunlight.
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Report
(4 results)
Research Products
(19 results)
