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过氧化氢对小鼠伤口愈合的影响与氧化损伤的关系。

Effects of hydrogen peroxide on wound healing in mice in relation to oxidative damage.

机构信息

Department of Biochemistry, National University of Singapore, Singapore, Singapore.

出版信息

PLoS One. 2012;7(11):e49215. doi: 10.1371/journal.pone.0049215. Epub 2012 Nov 13.

Abstract

It has been established that low concentrations of hydrogen peroxide (H(2)O(2)) are produced in wounds and is required for optimal healing. Yet at the same time, there is evidence that excessive oxidative damage is correlated with poor-healing wounds. In this paper, we seek to determine whether topical application of H(2)O(2) can modulate wound healing and if its effects are related to oxidative damage. Using a C57BL/6 mice excision wound model, H(2)O(2) was found to enhance angiogenesis and wound closure at 10 mM but retarded wound closure at 166 mM. The delay in closure was also associated with decreased connective tissue formation, increased MMP-8 and persistent neutrophil infiltration. Wounding was found to increase oxidative lipid damage, as measured by F(2)-isoprostanes, and nitrative protein damage, as measured by 3-nitrotyrosine. However H(2)O(2) treatment did not significantly increase oxidative and nitrative damage even at concentrations that delay wound healing. Hence the detrimental effects of H(2)O(2) may not involve oxidative damage to the target molecules studied.

摘要

已经证实,低浓度的过氧化氢(H(2)O(2))在伤口中产生,是最佳愈合所必需的。然而,与此同时,有证据表明,过度的氧化损伤与愈合不良的伤口有关。在本文中,我们试图确定局部应用 H(2)O(2)是否可以调节伤口愈合,以及其作用是否与氧化损伤有关。使用 C57BL/6 小鼠切除伤口模型,发现 H(2)O(2)在 10mM 时增强血管生成和伤口闭合,但在 166mM 时延迟伤口闭合。闭合延迟还与结缔组织形成减少、MMP-8 增加和持续的中性粒细胞浸润有关。如 F(2)-异前列腺素所测量的那样,伤口会增加脂质的氧化损伤,如 3-硝基酪氨酸所测量的那样,会增加蛋白质的硝化损伤。然而,即使在延迟伤口愈合的浓度下,H(2)O(2)处理也没有显著增加氧化和硝化损伤。因此,H(2)O(2)的有害作用可能不涉及研究的靶分子的氧化损伤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5695/3496701/3868cbb2d2d2/pone.0049215.g001.jpg

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