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  Alternative pathways as mechanism next term for the negative effects associated with overexpression of superoxide dismutase

Kowald, A., Lehrach, H., & Klipp, E. (2005). Alternative pathways as mechanism next term for the negative effects associated with overexpression of superoxide dismutase. Journal of Theoretical Biology (London), 238(4), 828-840. doi:10.1016/j.jtbi.2005.06.034.

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資料種別: 学術論文
その他のタイトル : J Theor Biol

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Kowald et al. - J Theor Biol.pdf (全文テキスト(全般)), 337KB
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https://hdl.handle.net/11858/00-001M-0000-0010-85CE-C
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Kowald et al. - J Theor Biol.pdf
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application/pdf / [MD5]
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 作成者:
Kowald, Axel1, 著者           
Lehrach, Hans2, 著者           
Klipp, Edda1, 著者           
所属:
1Independent Junior Research Groups (OWL), Max Planck Institute for Molecular Genetics, Max Planck Society, ou_1433554              
2Dept. of Vertebrate Genomics (Head: Hans Lehrach), Max Planck Institute for Molecular Genetics, Max Planck Society, ou_1433550              

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キーワード: Anti-oxidants; Aging; Free radicals; Transgenics
 要旨: One of the most important antioxidant enzymes is superoxide dismutase (SOD), which catalyses the dismutation of superoxide radicals to hydrogen peroxide. The enzyme plays an important role in diseases like trisomy 21 and also in theories of the mechanisms of aging. But instead of being beneficial, intensified oxidative stress is associated with the increased expression of SOD and also studies on bacteria and transgenic animals show that high levels of SOD actually lead to increased lipid peroxidation and hypersensitivity to oxidative stress. Using mathematical models we investigate the question how overexpression of SOD can lead to increased oxidative stress, although it is an antioxidant enzyme. We consider the following possibilities that have been proposed in the literature: (i) Reaction of H2O2 with CuZnSOD leading to hydroxyl radical formation. (ii) Superoxide radicals might reduce membrane damage by acting as radical chain breaker. (iii) While detoxifying superoxide radicals SOD cycles between a reduced and oxidized state. At low superoxide levels the intermediates might interact with other redox partners and increase the superoxide reductase (SOR) activity of SOD. This short-circuiting of the SOD cycle could lead to an increased hydrogen peroxide production. We find that only one of the proposed mechanisms is under certain circumstances able to explain the increased oxidative stress caused by SOD. But furthermore we identified an additional mechanism that is of more general nature and might be a common basis for the experimental findings. We call it the alternative pathway mechanism.

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言語: eng - English
 日付: 2005-08-08
 出版の状態: 出版
 ページ: -
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 識別子(DOI, ISBNなど): eDoc: 272001
DOI: 10.1016/j.jtbi.2005.06.034
 学位: -

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出版物 1

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出版物名: Journal of Theoretical Biology (London)
  出版物の別名 : J Theor Biol
種別: 学術雑誌
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出版社, 出版地: -
ページ: - 巻号: 238 (4) 通巻号: - 開始・終了ページ: 828 - 840 識別子(ISBN, ISSN, DOIなど): ISSN: 0022-5193