| Project/Area Number |
24591170
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| Research Category |
Grant-in-Aid for Scientific Research (C)
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| Allocation Type | Multi-year Fund |
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| Section | 一般 |
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| Research Field |
Respiratory organ internal medicine
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| Research Institution | Research Institute, International Medical Center of Japan |
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Principal Investigator |
OKAMOTO Tatsuya 独立行政法人国立国際医療研究センター, ICU・CCU・HCU 管理室, 医長 (30419634)
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| Co-Investigator(Kenkyū-buntansha) |
FUJII Shigemoto 東北大学, 大学院医学研究科, 准教授 (00325333)
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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 |
¥5,330,000 (Direct Cost: ¥4,100,000、Indirect Cost: ¥1,230,000)
Fiscal Year 2014: ¥1,820,000 (Direct Cost: ¥1,400,000、Indirect Cost: ¥420,000)
Fiscal Year 2013: ¥1,690,000 (Direct Cost: ¥1,300,000、Indirect Cost: ¥390,000)
Fiscal Year 2012: ¥1,820,000 (Direct Cost: ¥1,400,000、Indirect Cost: ¥420,000)
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| Keywords | 急性呼吸窮迫症候群 / 8-ニトロcGMP / 硫化水素イオン / 生体内ポリスルフィド / インフルエンザウイルス肺炎 / グルタチオン / システイン / 安定同位体希釈質量分析法 |
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| Outline of Final Research Achievements |
Reactive persulfides and polysulfides are formed endogenously in high amounts in mammalian cells and tissues. These reactive sulfur species were biosynthesized by two major sulfurtransferases: cystathionine beta-synthase and cystathionine gamma-lyase. Quantitation of these species indicates that high concentrations of glutathione persulfide and other cysteine persulfide and polysulfide derivatives in peptides/proteins were endogenously produced and maintained in the plasma, cells, and tissues of mammals. Because they quickly react with a recently described biologically generated electrophile 8-nitroguanosine 3',5'-cyclic monophosphate. These results indicate that persulfides are potentially important signaling/effector species, and because H2S can be generated from persulfide degradation, much of the reported biological activity associated with H2S may actually be that of persulfides. That is, H2S may act primarily as a marker for the biologically active of persulfide species.
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