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抗氧化生物因子对人牙龈成纤维细胞活性氧的抗氧化作用。

Antioxidant effects of antioxidant biofactor on reactive oxygen species in human gingival fibroblasts.

机构信息

Department of Endodontics, Nihon University School of Dentistry at Matsudo, 870-1, Sakaecho, Nishi-2, Matsudo, Chiba 271-8587, Japan.

出版信息

J Clin Biochem Nutr. 2011 May;48(3):209-13. doi: 10.3164/jcbn.10-85. Epub 2011 Apr 26.

DOI:10.3164/jcbn.10-85
PMID:21562640
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3082075/
Abstract

The purpose of this study was to investigate the effects of antioxidant biofactor (AOB) on reactive oxygen species (ROS). Generation of superoxide radical (O(2) (•-)) and hydroxyl radical ((•)OH) was determined using an electron spin resonance (ESR) spin-trapping method. AOB was added at different concentrations to these free radical generating systems. The generation of both O(2) (•-) and (•)OH was scavenged by the addition of AOB in a dose-dependent manner. These results indicate that AOB has strong antioxidant properties against these radicals. We further investigated the anti-oxidative effect of AOB on human gingival fibroblasts (HGFs). HGFs were treated for 3 h with α-MEM containing a combination of AOB and H(2)O(2) (AOB + H(2)O(2) group), containing H(2)O(2) (H(2)O(2) group), or containing AOB alone (AOB group). Non-stimulated HGFs were used as a control group. The number of surviving cells was in the order of the AOB group > control group > AOB + H(2)O(2) group > H(2)O(2) group. The level of expression of type I collagen mRNA and production of collagen were also in the order of the AOB group > control group > AOB + H(2)O(2) group > H(2)O(2) group. In conclusion, our results suggest that AOB may protect HGFs against oxidative stress by reducing stress-induced ROS.

摘要

本研究旨在探讨抗氧化生物因子(AOB)对活性氧(ROS)的影响。采用电子自旋共振(ESR)自旋捕获法测定超氧自由基(O2(•-))和羟自由基(•OH)的生成。将 AOB 以不同浓度加入这些自由基生成系统。O2(•-)和(•OH)的生成均随 AOB 的加入呈剂量依赖性清除。这些结果表明 AOB 对这些自由基具有很强的抗氧化特性。我们进一步研究了 AOB 对人牙龈成纤维细胞(HGFs)的抗氧化作用。HGFs 用含 AOB 和 H2O2(AOB+H2O2 组)、含 H2O2(H2O2 组)或仅含 AOB(AOB 组)的 α-MEM 处理 3 h。未刺激的 HGFs 用作对照组。存活细胞数的顺序为 AOB 组>对照组>AOB+H2O2 组>H2O2 组。I 型胶原 mRNA 的表达水平和胶原的产生也呈现 AOB 组>对照组>AOB+H2O2 组>H2O2 组的顺序。总之,我们的结果表明,AOB 可能通过减少应激诱导的 ROS 来保护 HGFs 免受氧化应激。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/874f/3082075/c7ad9d54c363/jcbn10-85f04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/874f/3082075/6ba124bce160/jcbn10-85f01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/874f/3082075/c44712f8ba21/jcbn10-85f02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/874f/3082075/eb7c1539b1fd/jcbn10-85f03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/874f/3082075/c7ad9d54c363/jcbn10-85f04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/874f/3082075/6ba124bce160/jcbn10-85f01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/874f/3082075/c44712f8ba21/jcbn10-85f02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/874f/3082075/eb7c1539b1fd/jcbn10-85f03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/874f/3082075/c7ad9d54c363/jcbn10-85f04.jpg

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