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Trial of Brain Redox Imaging and Estimation of Radiation-Induced Redox Change in Mouse Brain

https://repo.qst.go.jp/records/66116
https://repo.qst.go.jp/records/66116
b2b53680-1630-41ec-bf41-1c14c0120ec4
Item type 会議発表用資料 / Presentation(1)
公開日 2017-02-14
タイトル
タイトル Trial of Brain Redox Imaging and Estimation of Radiation-Induced Redox Change in Mouse Brain
言語
言語 jpn
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, Ken-ichiro

× Matsumoto, Ken-ichiro

WEKO 650927

Matsumoto, Ken-ichiro

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Nakamura, Mizuki

× Nakamura, Mizuki

WEKO 650928

Nakamura, Mizuki

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Ueno, Megumi

× Ueno, Megumi

WEKO 650929

Ueno, Megumi

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Nakanishi, Ikuo

× Nakanishi, Ikuo

WEKO 650930

Nakanishi, Ikuo

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Kamada, Tadashi

× Kamada, Tadashi

WEKO 650931

Kamada, Tadashi

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Yamada, Ken-ichi

× Yamada, Ken-ichi

WEKO 650932

Yamada, Ken-ichi

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Aoki, Ichio

× Aoki, Ichio

WEKO 650933

Aoki, Ichio

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松本 謙一郎

× 松本 謙一郎

WEKO 650934

en 松本 謙一郎

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中村 美月

× 中村 美月

WEKO 650935

en 中村 美月

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上野 恵美

× 上野 恵美

WEKO 650936

en 上野 恵美

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中西 郁夫

× 中西 郁夫

WEKO 650937

en 中西 郁夫

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鎌田 正

× 鎌田 正

WEKO 650938

en 鎌田 正

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青木 伊知男

× 青木 伊知男

WEKO 650939

en 青木 伊知男

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抄録
内容記述タイプ Abstract
内容記述 The in vivo T1-weighted contrasting abilities and signal decay behaviors of several nitroxyl contrast agents, which have been used as redox responsive contrast agents in several magnetic resonance-based imaging modalities, in mouse brain were compared. In addition, daily variations of redox behavior in mouse brain after irradiation of X-ray or carbon-ion beams (C-beam) were tried to estimate based on the in vivo reduction rate of amphiphilic nitroxyl contrast agents.
Injection solutions of five types of five-membered-ring nitroxyl contrast agents, i.e. 3-carboxy-2,2,5,5-tetramethylpyrrolidine-N-oxyl (CxP), 3-carbamoyl-2,2,5,5-tetramethylpyrrolidine-N-oxyl (CmP), 3-methoxy-carbonyl-2,2,5,5-tetramethylpyrrolidine-N-oxyl (MCP), acetoxymethyl-2,2,5,5-tetramethylpyrrolidine-N-oxyl-3-carboxylate (CxP-AM), and 4-(N-methylpiperidine)-2,2,5,5-tetramethylpyrroline-N-oxyl (23c), and a six-membered-ring nitroxyl contrast agent, i.e. 4-hydroxyl-2,2,6,6-tetramethylpiperidine-N-oxyl (TEMPOL), were prepared. The nitroxyl contrast agent was i.v. injected to a mouse through tail vein. Then, the distributions and pharmacokinetics of nitroxyl contrast agents were compared based on the time course of T1-weighted MRI. The MRI experiments using CMP or TEMPOL were repeated for mice irradiated by X-ray or C-beam to their head on several deferent timings, i.e. 1, 2, 4, 8 day(s) after irradiation. C-beam was irradiated at Heavy-Ion Medical Accelerator in Chiba (HIMAC, National Institute of Radiological Sciences/ National Institutes for Quantum and Radiological Science and Technology).
The blood-brain-barrier (BBB)-impermeable CxP could not be distributed in the brain. The slightly lipophilic CmP showed slight distribution only in the ventricle, but not in the medulla and cortex. The amphiphilic MCP and TEMPOL had good initial uniform distribution in the brain and showed typical 2-phase signal decay profiles. A brain-seeking nitroxyl probe, CxP-AM, showed an accumulating phase, and then its accumulation was maintained in the medulla and ventricle regions, but not in the cortex. The lipophilic 23c was well distributed in the cortex and medulla, but slightly in the ventricle, and showed relatively rapid linear signal decay.
Decay rates of MCP in mouse brain after irradiation of 8 Gy X-ray, 8 Gy C-beam or 16 Gy C-beams did not show marked clear changes, however relatively little decreasing were observed at day 1 and day 2 after irradiation. Decay rates of TEMPOL was increased 1 after irradiation then gradually recovered to the control level. MCP and TEMPOL showed opposite responses but the timing of redox change may be 1 or 2 days after irradiation.
Nitroxyl contrast agents equipped with a suitable lipophilic substitution group could be BBB-permeable functional contrast agents. MR redox imaging, which can estimate not only the redox characteristics but also the detailed distribution of the contrast agents, is a good candidate for a theranostic tool. Irradiation of ionized radiation to head could cause alternation of redox status in the brain. Detail of redox mechanisms were 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 第7回国際放射線神経生物学会大会
発表年月日
日付 2017-02-09
日付タイプ Issued
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