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  1. 学術雑誌
  2. Biological & Pharmaceutical Bulletin

Involvement of NO Generation in Aluminum-Induced Cell Death

https://hokuriku.repo.nii.ac.jp/records/538
https://hokuriku.repo.nii.ac.jp/records/538
5beed3fb-5674-4a31-b118-55ea280481b4
名前 / ファイル ライセンス アクション
Biological Biological & Pharmaceutical Bulletin 2007.08 (399.6 kB)
Item type 学術雑誌論文 / Journal Article(1)
公開日 2018-07-18
タイトル
タイトル Involvement of NO Generation in Aluminum-Induced Cell Death
タイトル
タイトル Involvement of NO Generation in Aluminum-Induced Cell Death
言語 en
言語
言語 eng
キーワード
言語 en
主題Scheme Other
主題 aluminum toxicity|nitric oxide
キーワード
言語 en
主題Scheme Other
主題 caspase
キーワード
言語 en
主題Scheme Other
主題 ascorbic acid
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
著者 Satoh, Eiko

× Satoh, Eiko

WEKO 491
e-Rad 20298368

Satoh, Eiko

en Satoh, Eiko

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Yasuda , Iho

× Yasuda , Iho

WEKO 492

Yasuda , Iho

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Yamada , Tomoko

× Yamada , Tomoko

WEKO 493

Yamada , Tomoko

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Suzuki , Yasuyuki

× Suzuki , Yasuyuki

WEKO 494

Suzuki , Yasuyuki

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Ohyashiki , Takao

× Ohyashiki , Takao

WEKO 495
e-Rad 00100488

Ohyashiki , Takao

en Ohyashiki , Takao

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Yasuda , Iho

× Yasuda , Iho

WEKO 496

en Yasuda , Iho

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Yamada , Tomoko

× Yamada , Tomoko

WEKO 497

en Yamada , Tomoko

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Suzuki , Yasuyuki

× Suzuki , Yasuyuki

WEKO 498

en Suzuki , Yasuyuki

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抄録
内容記述タイプ Abstract
内容記述 Previously, we have reported that the exposure of PC12 cells to the aluminum–maltolate complex (Al(maltol)3) results in decreased cell viability via the apoptotic cell death pathway. In this study, we have used several nitric oxide synthase (NOS) inhibitors and the NO generator diethylenetriamine NONOate (DETA NONOate) to examine whether or not intracellular nitric oxide (NO) generation is involved in the onset mechanism of Al(maltol)3-induced cell death. Cell viability was assessed by measuring lactate dehydrogenase (LDH) release and caspase-3 activity. Treatment of the cells with 150 μM Al(maltol)3 for 48 h resulted in intracellular NO generation. Exposure of the cells to DETA NONOate also induced a marked decrease in cell viability. Pre-treatment of the cells with a general NOS inhibitor or with a selective inducible NOS (iNOS) inhibitor effectively prevented Al(maltol)3-induced cell death. However, a neuronal NOS (nNOS) inhibitor did not exhibit any protective effect against Al(maltol)3-induced cell death. In addition, ascorbic acid markedly inhibited Al(maltol)3- and DETA NONOate-induced cell death. Based on these results, we discussed the involvement of intracellular NO generation in the onset mechanisms of Al(maltol)3-induced cell death.
書誌情報 en : Biological & Pharmaceutical Bulletin

巻 30, 号 8, p. 1390-1394, 発行日 2007-08
出版者
出版者 公益社団法人日本薬学会
ISSN
収録物識別子タイプ ISSN
収録物識別子 0918-6158
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