蒲公英、金银花和益母草抗氧化和抗炎作用的研究。复杂的

Sung Sin Huh, Young Il Kim
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摘要

目的:研究蒲公英、金银花和益母草的抗氧化和抗炎作用。复合物(TLL)在lps诱导的RAW264.7细胞中的表达。方法:采用FRAP法、DPPH自由基清除能力、ABTS自由基清除能力测定TLL的抗氧化活性。采用标准方法测定总多酚和类黄酮含量。通过NO生成、生物标志物生成(PGE2、IL-1β、IL-6、TNF-α)、mRNA表达水平(iNOS、COX-2、IL-1β、IL-6、TNF-α)和蛋白表达水平(ERK、JNK、p38)检测TLL的抗炎作用。结果:产水日粮总多酚含量为58.03±1.02 mg /g没食子酸当量(GAE)和16.58±0.60 mg /g槲皮素当量(QE)。在FRAP测定、DPPH和ABTS自由基清除活性中,观察到TLL呈浓度依赖性增加。为了探讨TLL对RAW 264.7细胞的抗氧化和抗炎作用,我们用TLL和LPS处理RAW 264.7细胞24小时。通过添加EZ-Cytox,测定了RAW 264.7细胞的细胞活力,在50、100、200 μ mol /毫升的TLL浓度下,细胞活力显著提高。与对照组相比,50、100、200 μ l浓度的TLL显著降低了NO、ROS、iNOS、IL-1β、IL-6、TNF-α、ERK、JNK和p38。在100、200毫升浓度下,PGE2和COX-2明显降低。结论:TLL配合物具有抗氧化和抗炎作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Study on Antioxidant and Anti-inflammatory Effects of Taraxacum platycarpum H. Dahlstedt, Lonicera japonica Thunberg and Leonurus japonicus Houtt. Complex
Objectives: This study was designed to experiment with the antioxidant and anti-inflammatory effects of Taraxacum platycarpum H. Dahlstedt, Lonicera japonica Thunberg, and Leonurus japonicus Houtt. complex (TLL) in LPS-induced RAW264.7 cell.Methods: The antioxidant activity of TLL was measured by FRAP assay, DPPH radical scavenging activity, ABTS radical scavenging activity. Total polyphenol and flavonoid contents of TLL were measured by using standard methods. The anti-inflammatory effects of TLL were measured by NO production, biomarker production (PGE2, IL-1β, IL-6, TNF-α), mRNA expression level (iNOS, COX-2, IL-1β, IL-6, TNF-α) and protein expression level (ERK, JNK, p38).Results: Total polyphenol and flavonoid contents in TLL were 58.03±1.02 ㎎ of Gallic acid equivalents (GAE)/g and 16.58±0.60 mg of Quercetin equivalents (QE)/g respectively. In FRAP assay, DPPH and ABTS radical scavenging activity, a concentration-dependent increase in TLL was observed. To explore antioxidant and anti-inflammatory effects of TLL, RAW 264.7 cells were treated with TLL and LPS for 24 hours. Cell viability of RAW 264.7 cells were measured by adding EZ-Cytox, It was remarkably increased at 50, 100, 200 ㎍/㎖ concentrations of TLL. NO, ROS, iNOS, IL-1β, IL-6, TNF-α, ERK, JNK and p38 were remarkably decreased at 50, 100, 200 ㎍/㎖ concentrations of TLL compared to the control group. PGE2 and COX-2 were remarkably decreased at 100, 200 ㎍/㎖ concentrationsConclusion: These results suggest that TLL complex has antioxidant and anti-inflammatory effects.
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