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Reaction of nitroxyl radicals and GSH; pH deendence

https://repo.qst.go.jp/records/70334
https://repo.qst.go.jp/records/70334
ea4798d4-6049-4a4f-a9d7-c68fdc8fca07
Item type 会議発表用資料 / Presentation(1)
公開日 2010-11-24
タイトル
タイトル Reaction of nitroxyl radicals and GSH; pH deendence
言語
言語 eng
資源タイプ
資源タイプ識別子 http://purl.org/coar/resource_type/c_c94f
資源タイプ conference object
アクセス権
アクセス権 metadata only access
アクセス権URI http://purl.org/coar/access_right/c_14cb
著者 Matsumoto, Kenichiro

× Matsumoto, Kenichiro

WEKO 690692

Matsumoto, Kenichiro

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Nakanishi, Ikuo

× Nakanishi, Ikuo

WEKO 690693

Nakanishi, Ikuo

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Krishna, Murali

× Krishna, Murali

WEKO 690694

Krishna, Murali

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松本 謙一郎

× 松本 謙一郎

WEKO 690695

en 松本 謙一郎

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中西 郁夫

× 中西 郁夫

WEKO 690696

en 中西 郁夫

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内容記述タイプ Abstract
内容記述 Nitroxyl radicals were utilized as redox probe in a field of in vivo EPR spectroscopy and imaging. Recently, utility of nitroxyl radicals as redox sensitive contrast agents for functional MRI were proposed and were getting interests. Detail reaction of nitroxyl radicals with each biological molecule, such as glutathione (GSH), were however not enough investigated. We have investigated temperature dependent reaction of nitroxyl radical with coexisting GSH. GSH can react with 2 molecules of a nitroxyl radical, and can eliminate EPR signal completely. Addition of K3Fe(CN)6 to the reaction mixture can not recover EPR signal of nitroxyl radical after the reaction with GSH. In this study, pH dependence of reduction of several nitroxyl radicals (TEMPO, TEMPOL, TEMPONE, carboxy-PROXYL, and carbamoyl-PROXYL) with coexisting glutathione at 37[deg]C was tested. The decay profiles of nitroxyl radicals were depending on pH. The reduction of nitroxyl radicals become faster in pH6 compared with pH7, except carboxy-PROXYL was not react in lower pH. Almost no reduction of nitroxyl radicals occurred in pH8. However, mechanism of reaction of nitroxyl radical and GSH is still in progress.
会議概要(会議名, 開催地, 会期, 主催者等)
内容記述タイプ Other
内容記述 SFRBM's 17th Annual Meeting/SFRRI's XV Biennial Meeting
発表年月日
日付 2010-11-21
日付タイプ Issued
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