| Project/Area Number |
12670142
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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 |
Pathological medical chemistry
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| Research Institution | Showa University (2002)
Kumamoto University (2000-2001) |
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Principal Investigator |
MIYAMOTO Yoichi Showa University, School of Dentistry, Lecturer, 歯学部, 講師 (20295132)
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| Co-Investigator(Kenkyū-buntansha) |
KAMIJO Ryutaro Showa University, School of Dentistry, Professor, 歯学部, 教授 (70233939)
KATAGIRI Takenobu Showa University, School of Dentistry, Associate Professor, 歯学部, 助教授 (80245802)
ITOH Kanami Showa University, School of Dentistry, Research Associate, 歯学部, 助手 (10349045)
MAEDA Hiroshi Kumamoto University, School of Medicine, Professor, 医学部, 教授 (90004613)
AKAIKE Takaaki Kumamoto University, School of Medicine, Associate professor, 医学部, 助教授 (20231798)
澤 智裕 熊本大学, 医学部, 助手 (30284756)
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| Project Period (FY) |
2000 – 2002
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| Project Status |
Completed (Fiscal Year 2002)
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| Budget Amount *help |
¥3,500,000 (Direct Cost: ¥3,500,000)
Fiscal Year 2002: ¥1,100,000 (Direct Cost: ¥1,100,000)
Fiscal Year 2001: ¥1,100,000 (Direct Cost: ¥1,100,000)
Fiscal Year 2000: ¥1,300,000 (Direct Cost: ¥1,300,000)
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| Keywords | NITROSOTHIOLS / NITRIC OXIDE / GLUTATHIONE / PEROXYNITRITE / MATRIX METALLOPROTEINASE / S-NITROSULFOXYDE / α_1-PROTEASE INHIBITOR / THIOL MODIFICATION / グルタチオン付加反応 / matrix metalloproteinase / NO / α1-プロテアーゼインヒビター / セルロプラスミン |
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| Research Abstract |
Nitric oxide (NO) exhibits multiple biological actions through formation of various intermediates derived from NO. Among them, we found that nitrosothiols (RSNOs), adducts of SH moiety of biological compounds and NO, could be formed efficiently via one-electron oxidation of NO catalyzed by ceruloplasmin, a major copper-containing protein in plasma. In addition, we identified S-oxiso-nitrosoglutathione [GS(O)NO] as a reaction product of glutathione and peroxynitrite (ONOO^-), an adduct of NO and superoxide. Furthermore, GS(O)NO activated matrix metalloproteinases (MMPs) through formation of dithiothreitol-resistant S-glutathionyl MMPs, indicating that ONOO^- exerts its tissue destructive effects via formation of S-oxo-nitrosothiols as well as direct nitration or oxidation of biological molecules. In the latter part of this project, we investigated the biological significance of nitrosative and nitrative stresses in inflammatory disorders including rheumatoid arthritis (RA), where NO production is accelerated. We could detect the expression of ceruloplasmin in chondrocytes, suggests the possible formation of nitrosothiols in the inflammatory foci of RA. On the other hand, it is reported that α_1-protease inhibitor (α_1PI) level in joint is increased in RA patients. As we reported earlier, α1PI is readily S-niotrosylated by NO and S-nitrosylated α1PI shows tissue protective effects in vitro and in vivo. In this study we studied nitrosylation of methionine-oxidized α1PI [α_1PI-Met(O)] and the biological activities of this reaction products, because RA joints are thought to be under highly oxidative conditions. The efficacy of S-nitrosylation of α_1PI-Met(O) was around 80% of that of α1PI. Interestingly, antibacterial activity of S- nitrosylated α1PI-Met(O) in vitro was 100 times more potent than that of S-nitrosylated α_1PI. The further study will be performed to clarify the pathophysiological roles of S-nitrosylated α_1PI-Met(O).
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