天然产物研究与开发 ›› 2021, Vol. 33 ›› Issue (增刊2): 23-31.

• 研究论文 • 上一篇    下一篇

参芍抗敏剂的抗炎作用研究

郑木创1,毕凡星2,刘英3,金敏蓉4,翟春涛4*   

  1. 1广东雅丽洁精细化工有限公司;2广东芭薇生物科技股份有限公司;3广东施露兰化妆品有限公司,广东 515000;
    4莱博药妆技术(上海)股份有限公司,上海 201401

  • 出版日期:2021-12-28 发布日期:2021-11-23

Study on the anti-inflammatory effect of the Shengshao antisensitizer

ZHENG Mu-chuang1,BI Fan-xing2,LIU Ying3,JIN Min-rong4,ZHAI Chun-tao4*   

  1. 1Guangdong Yalget Fine Chemical Co.,Ltd.;2Guangdong Bawei Biotechnology Corporation;3Guangdong Siloran Cosmetics Co.,Ltd.,Guangdong 515000,China; 4LB Cosmeceutical Technology Co.,Ltd.,Shanghai 201401,China


  • Online:2021-12-28 Published:2021-11-23

摘要:

为研究参芍抗敏剂的抗炎作用,通过探索参芍抗敏剂对钙调磷酸酶通路的活化水平及对TNF-α诱导的HaCaT细胞炎症反应的作用,来探索参芍抗敏剂的抗炎作用。结果显示,参芍抗敏剂在1∶1 000时就有与125 μM他克莫司(FK506)相同的抑制效果;参芍抗敏剂对TNF-α处理的细胞内磷酸化P38的量有所减少,且随着药物浓度的降低而相对升高,其中0.2%参芍抗敏剂作用最显著;参芍抗敏剂对TNF-α刺激引起胞质中NF-κB激活入核现象有显著抑制作用,且随着浓度的升高,入核比例下降,相同浓度的芍药苷和德敏舒具有相同作用;参芍抗敏剂、芍药苷和德敏舒可以抑制TNF-α刺激后细胞内源TNF-α表达量,其中0.05%参芍抗敏剂和芍药苷作用最明显;参芍抗敏剂、芍药苷和德敏舒可以抑制TNF-α刺激的IL-6mRNA的相对表达,其中随着参芍抗敏剂浓度的增加而逐渐下降,0.1%参芍抗敏剂作用和芍药苷组作用相当,而德敏舒组作用更显著;参芍抗敏剂、芍药苷和德敏舒对TNF-α刺激的IL-8mRNA表达量显著下降;参芍抗敏剂、芍药苷和德敏舒对TNF-α诱导的IL-1α没有显著的抑制作用;参芍抗敏剂、芍药苷和德敏舒可以对TNF-α引起的COX-2表达有显著的抑制作用。因此,参芍抗敏剂具有较好的抗炎作用。


关键词: 参芍抗敏剂, 抗炎作用, 钙调磷酸酶通路, TNF-α

Abstract:

In order to study the anti-inflammatory effect of the Shengshao antisensitizer,the anti-inflammatory effect of the Shengshao antisensitizer was explored by exploring the activation level of calcineurin pathway and its effect on TNF-α-induced inflammatory response of HaCaT cells.Results showed that the same inhibitory effect as 125 μM tacromox (FK506) was observed at 1∶1 000.The amount of intracellular phosphorylation of P38 treated with TNF-α was decreased and increased with the decrease of the concentration of TNF-α,and 0.2% of them had the most significant effect.The Shengshao antisensitizer had a significant inhibitory effect on the nucleation phenomenon of NF-κB activation in cytoplasm induced by TNF-α stimulation,and the nucleation ratio decreases with the increase of concentration.Paeoniflorin and SymCalmin at the same concentration have the same effect.The Shengshao antisensitizer,paeoniflorin and SymCalmin could inhibit the intracellular expression of TNF-α after TNF-α stimulation,among which 0.05% of the Shengshao antisensitizer and paeoniflorin have the most obvious effects.The relative expression of IL-6 mRNA stimulated by TNF-α could be inhibited by the Shengshao antisensitizer,paeoniflorin and deminshu,among which,the effects of the Shengshao antisensitizer was decreased gradually with the increase of the concentration.The effect of the Shengshao antisensitizer was equivalent to that of paeoniflorin group,and that of deminshu group was more significant.The expression level of IL-8 mRNA stimulated by the Shengshao antisensitizer,paeoniflorin and deminshu was significantly decreased.The Shengshao antisensitizer,paeoniflorin and SymCalmin had no significant inhibitory effect on TNF-α induced IL-1α.The Shengshao antisensitizer,paeoniflorin and SymCalmin showed significant inhibitory effects on COX-2 expression induced by TNF-α.Therefore,the Shengshao antisensitizer has better anti-inflammatory effects.

Key words: Shengshao antisensitizer, antiinflammatory, calcineurin pathway, TNF

中图分类号:  R961.1