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  1. 原著論文

Probing the intracellular redox status of tumors with magnetic resonance imaging and redox-sensitive contrast agents

https://repo.qst.go.jp/records/48502
https://repo.qst.go.jp/records/48502
be117e98-c4e8-44da-bca3-f2c6209fec92
Item type 学術雑誌論文 / Journal Article(1)
公開日 2018-02-14
タイトル
タイトル Probing the intracellular redox status of tumors with magnetic resonance imaging and redox-sensitive contrast agents
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_6501
資源タイプ journal article
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 Hyodo, Fuminori

× Hyodo, Fuminori

WEKO 487593

Hyodo, Fuminori

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Matsumoto, Ken-ichiro

× Matsumoto, Ken-ichiro

WEKO 487594

Matsumoto, Ken-ichiro

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Matsumoto, Atsuko

× Matsumoto, Atsuko

WEKO 487595

Matsumoto, Atsuko

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Mitchell, James

× Mitchell, James

WEKO 487596

Mitchell, James

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Krishna, Murali

× Krishna, Murali

WEKO 487597

Krishna, Murali

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松本 謙一郎

× 松本 謙一郎

WEKO 487598

en 松本 謙一郎

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松本 厚子

× 松本 厚子

WEKO 487599

en 松本 厚子

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抄録
内容記述タイプ Abstract
内容記述 Nitroxide radicals are paramagnetic contrast agents, used in magnetic resonance imaging (MRI), that also exert antioxidant effects. Participating in cellular redox reactions, they lose their ability to probide contrast as a function of time after administration. In this study, the rate of contrast loss was correlated to the reducing power of the tissue or the "redox status." The preferential reduction of nitroxides in tumors compared with nomal tissue was observed by MRI. The influence of the structure of the nitroxide on the reduction reate was investigated by MRI using two cell-permeable nitroxides, 4-hydroxy-2,2,6,6-tetramethyl-1-piperidynyloxyl (Tempol) and 3-carbamoyl-2,2,5,5-tetramethylpyrrolidine-1-oxyl (3CP), and one cell-impermeable nitroxide, 3-carboxy-2,2,5,5-tetramethylpyrrolidine-1-oxyl (3CxP). Pharmacokinetic images of these nitroxides in normal tissue, tumor, kidney, and artery regions in mice were simultaneously obtained using MRI. The decay of Tempol and 3CP in tumor tissue was significantly faster than in normal tissue. No significant change in the total nitroxide (oxidized + reduced forms) was noted from tissue extracts, suggesting that the loss in contrast as a function of time is a result of intracellulat bioreduction. however, in the case of 3CxP (membrane impermeable), there was no difference in the reduction rates between normal and tumor tissue. The time course of T1 enhancement by 3CxP and the total amount of 3CxP (oxidized + reduced) in the femoral region showed similar pharmacokinetics. These results show that the differential bioreduction of cell-permeable nitroxides in tumor and normal tissue is supported by intracellular processes and the reduction rates are a means by shich the intracellular redox status can be assessed noninvasively.
書誌情報 Cancer Research

巻 66, 号 20, p. 9921-9928, 発行日 2006-10
ISSN
収録物識別子タイプ ISSN
収録物識別子 0008-5472
PubMed番号
識別子タイプ PMID
関連識別子 17047054
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