Evaluation on Anti-oxidant Activity and Anti-inflammatory Effects for the New Formulation of Gamisoyosan

H. Choi, Se‐Jin Kim, In-su Kim, Ji-Beom Lee, Jong-Beom Kim, S. Moon, Hwa-Dong Lee
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引用次数: 2

Abstract

Objectives : Gamisoyosan (GMS) is a useful prescription for treating insomnia, dysmenorrhea and infertility induced by a stress. Also, GMS has been used traditionally to improve systemic circulation and biological energy production. The purpose of this study was to assess the anti-oxidant activity and anti-inflammatory effects of Gamisoyosan Formulation (Soft extract, GMS-SE). Methods : The biological activities such as anti-oxidant and anti-inflammatory effects were measured through cell line-based in vitro assay. We investigated the anti-oxidant properties of GMS-SE on the 1,1-diphenyl-2-picryhydrazyl (DPPH) radical, contents of total flavonoid and polyphenol. GMS-SE compared to butyl hydroxy anizole (BHA). Furthermore, based on this result the anti-inflammatory effects of GMS-SE have verified by mechanism from LPS-treated Raw264.7 macrophages. Results : The anti-oxidant activities of GMS-SE increased markedly, in a dose-dependent manner. The GMS-SE showed significant scavenging activity (GMS-SE 500 ㎍/㎖ : 32.77±1.65%, GMS-SE 1000 ㎍/㎖ : 45.06±1.04% and BHA 100 ㎍/㎖ : 39.25±2.41% for DPPH assay). and, The total phenolic compound and flavonoids contents of GMS-SE were 73.93±6.87 ㎍/㎎ and 698.75±6.78 ㎍/㎎. GMS-SE which is LPS has diminished in the LPS-induced release of inflammatory mediators (NO, iNOS, COX2 and PGE2) and pro-inflammatory cytokines (TNF-α, IL-6 and IL-1β) from the RAW264.7 macrophages. Moreover, GMS-SE inhibited the activation of phosphorylation of p38 and ERK MAPKs by induced LPS. Conclusion : The present results indicate that GMS-SE has an anti-oxidant and anti-inflammatory properties, therefore may be beneficial in diseases which related to oxidative stress-mediated inflammatory disorders.
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新配方味异糖的抗氧化和抗炎作用评价
目的:Gamisoyosan (GMS)是治疗应激性失眠、痛经、不孕症的有效方药。此外,GMS传统上被用于改善体循环和生物能源生产。本研究的目的是评估Gamisoyosan制剂(软提取物,GMS-SE)的抗氧化活性和抗炎作用。方法:采用体外细胞系法测定其抗氧化、抗炎等生物活性。研究了GMS-SE对1,1-二苯基-2-苦酰肼(DPPH)自由基、总黄酮和多酚含量的抗氧化性能。GMS-SE与丁基羟基苯甲酸(BHA)的比较。在此基础上,通过lps处理Raw264.7巨噬细胞,验证了GMS-SE的抗炎作用机制。结果:GMS-SE的抗氧化活性明显增强,且呈剂量依赖性。GMS-SE有明显的清除活性(GMS-SE 500㎍/毫升:32.77±1.65%,GMS-SE 1000还债还债/毫升:45.06±1.04%,BHA 100还债还债/毫升:39.25±2.41%)。GMS-SE的总酚类化合物和黄酮类化合物含量分别为73.93±6.87和698.75±6.78㎍/㎎。LPS诱导的炎症介质(NO, iNOS, COX2和PGE2)和促炎细胞因子(TNF-α, IL-6和IL-1β)从RAW264.7巨噬细胞中释放减少。此外,GMS-SE还能抑制LPS对p38和ERK MAPKs磷酸化的激活。结论:GMS-SE具有抗氧化和抗炎作用,可能对氧化应激介导的炎症相关疾病有一定的治疗作用。
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