解毒祛瘀子饮方通过NOTCH1/NF-κB通路抑制巨噬细胞炎症活性

Sijia Fang , Lina Ji , Shan Wu , Xiaoxuan Yang , Kepeng Yang , Yongsheng Fan
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引用次数: 0

摘要

解毒祛瘀子饮方(JP)是一种中药方剂,用于治疗系统性红斑狼疮(SLE)已有几十年的历史,其有效性和安全性已在临床实践中得到证实。然而,人们对其分子机制知之甚少。目的探讨JP对巨噬细胞炎症活性及NOTCH1/NF-κB通路的影响。方法制备jp处理血清,确定其最佳浓度。考虑到大鼠血清中活性成分可能影响结果,同时制备不含JP成分的对照血清。用脂多糖(LPS)激活RAW264.7,并分别用DAPT (NOTCH1阻滞剂)、对照血清和jp处理血清干扰细胞。采用实时逆转录聚合酶链式反应(RT-PCR)、western blotting (WB)、酶联免疫吸附试验(ELISA)和Griess法检测干预后NOTCH1和RBPJ的表达、NF-κB的核易位以及细胞外il - 6、TNFα和NO的释放情况。结果DAPT和jp处理血清均能显著抑制LPS诱导的NOTCH1和RBPJ的表达以及NF-κB的核易位,导致il - 6、TNFα和NO的释放减少,而对照血清对巨噬细胞活性和NOTCH1/NF-κB通路影响不大。结论JP对巨噬细胞活化和促炎反应的影响,提示JP的分子机制可能与抑制NOTCH1/NF-κB通路有关。此外,已有研究表明,芍药苷和阿魏酸是JP的主要有效成分。在后续实验中,我们将进一步探讨这两种成分对MRL/lpr小鼠及巨噬细胞活性的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Jieduquyuziyin Prescription Suppresses the Inflammatory Activity of Macrophages via NOTCH1/NF-κB Pathway

Background

Jieduquyuziyin prescription (JP) is a traditional Chinese medicine (TCM) formula, which has been applied to the treatment of systemic lupus erythematosus (SLE) for decades, and its efficacy and safety have been confirmed in clinical practice. However, little is known about its molecular mechanism.

Objective

To explore the effects of JP on macrophages' inflammatory activity and NOTCH1/NF-κB pathway.

Methods

The JP-treated serum was prepared to determine its optimal concentration. Given the fact that active components in rats' serum might affect the results, control serum without JP components was prepared simultaneously. Lipopolysaccharide (LPS) was used to activate RAW264.7, and the cells were interfered with DAPT (NOTCH1 blocker), control serum, and JP-treated serum, respectively. After the above intervention, the expression of NOTCH1 and RBPJ, the nuclear translocation of NF-κB, and the extracellular release of IL6, TNFα, and NO, was evaluated by real-time reverse transcription-polymerase chain reaction (RT-PCR), western blotting (WB), enzyme-linked immunosorbent assay (ELISA), and Griess method.

Results

Both DAPT and JP-treated serum could significantly suppress the expression of NOTCH1 and RBPJ induced by LPS, as well as the nuclear translocation of NF-κB, leading to the decreased release of IL6, TNFα, and NO, while control serum had little effect on macrophage activity and NOTCH1/NF-κB pathway.

Conclusion

These results demonstrated the effects of JP on macrophage activation and pro-inflammatory response and suggested that the molecular mechanism of JP might attribute to the inhibition of the NOTCH1/NF-κB pathway. Besides, previous studies suggested that paeoniflorin and ferulic acid are two major effective components in JP. In subsequent experiments, we would further explore the effects of these two components on MRL/lpr mice and macrophage activity.

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来源期刊
Clinical complementary medicine and pharmacology
Clinical complementary medicine and pharmacology Complementary and Alternative Medicine
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