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探索多糖对人皮肤成纤维细胞中血红素加氧酶诱导的氧化应激的保护和修复机制。

Exploring the Protective and Reparative Mechanisms of Polysaccharides Against HO-Induced Oxidative Stress in Human Skin Fibroblasts.

作者信息

Shi Xiuqin, Cheng Wenjing, Wang Qian, Zhang Jiachan, Wang Changtao, Li Meng, Zhao Dan, Wang Dongdong, An Quan

机构信息

Chemistry and Materials Engineering, Beijing Technology and Business University, Beijing, 100048, People's Republic of China.

Yunnan Baiyao Group Co., Ltd, Kunming, 650000, People's Republic of China.

出版信息

Clin Cosmet Investig Dermatol. 2021 Oct 14;14:1481-1496. doi: 10.2147/CCID.S334527. eCollection 2021.

Abstract

BACKGROUND

() is one of China's traditional medicinal materials. polysaccharide has a wide range of promising pharmacological applications. However, there are many kinds of and they contain different kinds of polysaccharides. The biological mechanism through which polysaccharides (GLP) is able to protect human skin fibroblasts (HSFs) from HO-induced oxidative damage is still unclear.

METHODS

Six polysaccharides were obtained from to evaluate their free radical scavenging ability (DPPH free radical, ABTS free radical, hydroxyl-free radical, superoxide anion-free radical) in vitro, and their protective and reparative effects on oxidative damage induced by HO in human skin fibroblasts. One polysaccharide was selected to detect oxidative damage markers and gene expression in the Keap1-Nrf2/ARE signaling pathway in HSFs.

RESULTS

All six polysaccharides showed the ability to scavenge free radicals and enhance the tolerance of human skin fibroblasts to H2O2 damage. Among them, GLP1 was selected and separated into two components (GLP1I and GLP1II). The results showed that GLP1, GLP1I and GLPII could significantly reduce the levels of reactive oxygen species (ROS) and malondialdehyde (MDA). The protective effect of GLP1II was stronger than that of positive control vitamin C. In addition, GLP1, GLP1I and GLP1II could significantly increase the levels of superoxide dismutase (SOD), catalase (CAT) and glutathione peroxidase (GSH-Px). And GLP1I works best in both ways. Meanwhile, Nrf2, a key regulator of keAP1-NRF2/ARE signaling pathway, was activated, while Keap1, a negative regulator, was inhibited, thus promoting the expression of downstream antioxidant enzyme genes (GSTs, GCLs, Nqo1, and Ho-1).

CONCLUSION

The results showed that GLP could protect human skin fibroblasts from oxidative damage caused by HO peroxide by enhancing enzyme activity and activating Keap1-Nrf2/ARE signaling pathway. GLP will act as a natural antioxidant to protect the skin from oxidative stress damage.

摘要

背景

()是中国传统药材之一。多糖具有广泛且前景广阔的药理应用。然而,()种类繁多,且含有不同种类的多糖。()多糖(GLP)能够保护人皮肤成纤维细胞(HSFs)免受过氧化氢(HO)诱导的氧化损伤的生物学机制仍不清楚。

方法

从()中获得六种多糖,以评估它们在体外的自由基清除能力(DPPH自由基、ABTS自由基、羟自由基、超氧阴离子自由基),以及它们对人皮肤成纤维细胞中由HO诱导的氧化损伤的保护和修复作用。选择一种多糖检测人皮肤成纤维细胞中Keap1-Nrf2/ARE信号通路中的氧化损伤标志物和基因表达。

结果

所有六种多糖均表现出清除自由基的能力,并增强了人皮肤成纤维细胞对H2O2损伤的耐受性。其中,GLP1被选取并分离为两个组分(GLP1I和GLP1II)。结果表明,GLP1、GLP1I和GLPII均可显著降低活性氧(ROS)和丙二醛(MDA)水平。GLP1II的保护作用强于阳性对照维生素C。此外,GLP1、GLP1I和GLP1II均可显著提高超氧化物歧化酶(SOD)、过氧化氢酶(CAT)和谷胱甘肽过氧化物酶(GSH-Px)水平。且GLP1I在这两方面效果最佳。同时,Keap1-NRF2/ARE信号通路的关键调节因子Nrf2被激活,而负调节因子Keap1被抑制,从而促进下游抗氧化酶基因(GSTs、GCLs、Nqo1和Ho-1)的表达。

结论

结果表明,GLP可通过增强酶活性和激活Keap1-Nrf2/ARE信号通路来保护人皮肤成纤维细胞免受过氧化氢诱导的氧化损伤。GLP将作为一种天然抗氧化剂保护皮肤免受氧化应激损伤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/552a/8525518/fbfefd94917f/CCID-14-1481-g0001.jpg

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