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Effects of S-glutathionylation on the passive force–length relationship in skeletal muscle fibres of rats and humans

https://hiroshima.repo.nii.ac.jp/records/2007414
https://hiroshima.repo.nii.ac.jp/records/2007414
5ad1e2a6-600d-44c6-b7ac-2b7fc61604e1
名前 / ファイル ライセンス アクション
JMRCM_41_239.pdf JMRCM_41_239.pdf (1.2 MB)
Item type デフォルトアイテムタイプ_(フル)(1)
公開日 2023-03-18
タイトル
タイトル Effects of S-glutathionylation on the passive force–length relationship in skeletal muscle fibres of rats and humans
言語 en
作成者 Watanabe, Daiki

× Watanabe, Daiki

en Watanabe, Daiki

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Lamboley, Cedric R.

× Lamboley, Cedric R.

en Lamboley, Cedric R.

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Lamb, Graham D.

× Lamb, Graham D.

en Lamb, Graham D.

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アクセス権
アクセス権 open access
アクセス権URI http://purl.org/coar/access_right/c_abf2
権利情報
権利情報 This is not the published version. Please cite only the published version. この論文は出版社版ではありません。引用の際には出版社版をご確認、ご利用ください。
主題
主題Scheme Other
主題 Oxidative stress
主題
主題Scheme Other
主題 Muscle elasticity
主題
主題Scheme Other
主題 Skinned fbre
主題
主題Scheme Other
主題 Titin
主題
主題Scheme Other
主題 Passive force
内容記述
内容記述 This study investigated the efect of S-glutathionylation on passive force in skeletal muscle fbres, to determine whether activity-related redox reactions could modulate the passive force properties of muscle. Mechanically-skinned fbres were freshly obtained from human and rat muscle, setting sarcomere length (SL) by laser difraction. Larger stretches were required to produce passive force in human fbres compared to rat fbres, but there were no fbre-type diferences in either species. When fbres were exposed to glutathione disulfde (GSSG; 20 mM, 15 min) whilst stretched (at a SL where passive force reached~20% of maximal Ca2+-activated force, denoted as SL20 % max), passive force was subsequently decreased at all SLs in both type I and type II fbres of rat and human (e.g., passive force at SL20 % max decreased by 12 to 25%). This decrease was fully reversed by subsequent reducing treatment with dithiothreitol (DTT; 10 mM for 10 min). If freshly skinned fbres were initially treated with DTT, there was an increase in passive force in type II fbres (by 10±3% and 9±2% in rat and human fbres, respectively), but not in type I fbres. These results indicate that (i) S-glutathionylation, presumably in titin, causes a decrease in passive force in skeletal muscle fbres, but the reduction is relatively smaller than that reported in cardiac muscle, (ii) in rested muscle in vivo, there appears to be some level of reversible oxidative modifcation, probably involving S-glutathionylation of titin, in type II fbres, but not in type I fbres.
言語 en
内容記述
内容記述タイプ Other
内容記述 We thank the National Health and Medical Research Council of Australia for financial support (Grant No. 1085331).
出版者
出版者 Springer
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
出版タイプ
出版タイプ AO
出版タイプResource http://purl.org/coar/version/c_b1a7d7d4d402bcce
関連情報
識別子タイプ DOI
関連識別子 10.1007/s10974-019-09563-5
関連情報
識別子タイプ DOI
関連識別子 https://doi.org/10.1007/s10974-019-09563-5
収録物識別子
収録物識別子タイプ ISSN
収録物識別子 0142-4319
収録物識別子
収録物識別子タイプ ISSN
収録物識別子 1573-2657
開始ページ
開始ページ 239
書誌情報 Journal of Muscle Research and Cell Motility
Journal of Muscle Research and Cell Motility

巻 41, p. 239-250, 発行日 2019-11-02
旧ID 51508
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