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富含异黄酮的大驳骨提取物通过清除活性氧和抑制 MAP 激酶和 MMP 表达来减轻 UVB 诱导的皮肤损伤。

Isoflavonoid-Rich Flemingia macrophylla Extract Attenuates UVB-Induced Skin Damage by Scavenging Reactive Oxygen Species and Inhibiting MAP Kinase and MMP Expression.

机构信息

Department of Cosmeceutics, China Medical University, Taichung 404, Taiwan.

出版信息

Evid Based Complement Alternat Med. 2013;2013:696879. doi: 10.1155/2013/696879. Epub 2013 Jul 1.

DOI:10.1155/2013/696879
PMID:23935672
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3713360/
Abstract

In this study, we investigated the antioxidant activity and anti-photoaging properties of an extract of Flemingia macrophylla, a plant rich in isoflavonoid content. Pretreatment of fibroblasts with Flemingia macrophylla extract (FME) inhibited elastase activity, promoted the protein expression of type I procollagen, and attenuated the phosphorylation of mitogen-activated protein (MAP) kinase and the protein expression of matrix-metalloproteinase- (MMP-) 1, 3, and 9. The IC50 values were 2.1  μ g/mL for DPPH radical scavenging ability, 366.8  μ g/mL for superoxide anion scavenging ability, 178.9  μ g/mL for hydrogen peroxide scavenging ability, and 230.9  μ g/mL for hydroxyl radical scavenging ability. Also, exposure of erythrocytes to various concentrations of FME (50-500  μ g/mL) resulted in a dose- and time-dependent inhibition of AAPH-induced hemolysis. In human fibroblasts, FME at 10  μ g/mL was shown to be a potent scavenger of UV-induced reactive oxygen species (ROS). The antioxidant and anti-photoaging properties of FME make it an ideal anti-intrinsic aging and anti-photoaging agent.

摘要

在这项研究中,我们研究了富含异黄酮的 Flemingia macrophylla 提取物的抗氧化活性和抗光老化特性。Flemingia macrophylla 提取物 (FME) 预处理纤维母细胞可抑制弹性蛋白酶活性,促进 I 型原胶原的蛋白表达,并减弱丝裂原激活蛋白 (MAP) 激酶的磷酸化和基质金属蛋白酶- (MMP-) 1、3 和 9 的蛋白表达。DPPH 自由基清除能力的 IC50 值为 2.1 μ g/mL,超氧阴离子清除能力为 366.8 μ g/mL,过氧化氢清除能力为 178.9 μ g/mL,羟基自由基清除能力为 230.9 μ g/mL。此外,将红细胞暴露于不同浓度的 FME(50-500 μ g/mL)会导致 AAPH 诱导的溶血呈剂量和时间依赖性抑制。在人成纤维细胞中,10 μ g/mL 的 FME 可有效清除 UV 诱导的活性氧 (ROS)。FME 的抗氧化和抗光老化特性使其成为理想的抗内在衰老和抗光老化剂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/993b/3713360/e37577921f54/ECAM2013-696879.007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/993b/3713360/e28068137e57/ECAM2013-696879.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/993b/3713360/6e423ca83114/ECAM2013-696879.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/993b/3713360/54be89e48fbe/ECAM2013-696879.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/993b/3713360/d0b9a906220c/ECAM2013-696879.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/993b/3713360/78e204fcb01c/ECAM2013-696879.005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/993b/3713360/3e177494fe58/ECAM2013-696879.006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/993b/3713360/e37577921f54/ECAM2013-696879.007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/993b/3713360/e28068137e57/ECAM2013-696879.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/993b/3713360/6e423ca83114/ECAM2013-696879.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/993b/3713360/54be89e48fbe/ECAM2013-696879.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/993b/3713360/d0b9a906220c/ECAM2013-696879.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/993b/3713360/78e204fcb01c/ECAM2013-696879.005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/993b/3713360/3e177494fe58/ECAM2013-696879.006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/993b/3713360/e37577921f54/ECAM2013-696879.007.jpg

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