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连翘汤的抗炎活性与 Nrf2 和 A20 有关。

Anti-inflammatory activity of the decoction of Forsythia suspensa (Thunb.) Vahl is related to Nrf2 and A20.

机构信息

Department of Clinical Korean Medicine, Graduate School, Kyung Hee University, KHU Rd 23, Seoul 02447, Republic of Korea.

School of Korean Medicine, Pusan National University, PNU Rd 49, Yangsan 50612, Republic of Korea.

出版信息

J Ethnopharmacol. 2018 Dec 5;227:97-104. doi: 10.1016/j.jep.2018.08.027. Epub 2018 Aug 24.

Abstract

ETHNOPHARMACOLOGICAL RELEVANCE

The water extract of Forsythiae Fructus (WFF) is an herbal remedy that is prescribed to treat various inflammatory diseases in traditional Chinese medicine. Although the anti-inflammatory activity of WFF has been reported, the underlying mechanisms for the activity remain unclear. Here, we examined whether the anti-inflammatory activity of WFF is associated with Nrf2, an anti-inflammatory factor, and A20, an ubiquitin-regulator protein that inhibits signaling cascades of endotoxin or cytokines.

MATERIALS AND METHODS

The water extract of Forsythia suspensa (Thunb.) Vahl was prepared and fingerprinted by HPLC. Cytotoxicity and intracellular ROS induced by WFF were determined by MTT and FACS analyses, respectively. Nuclear and cytoplasmic proteins were analyzed by immunoblot. Expression of mRNA was analyzed by a semi-quantitative RT-PCR. Expression of proteins or genes was quantitated by Image J.

RESULTS

WFF activated Nrf2, inducing the expression of Nrf2-dependent genes, such as HO-1, NQO1, and GCLC in RAW 264.7 cells. On the other hand, WFF suppressed NF-κB induced by LPS or TNF-α, which was coincided with the expression of A20. Conversely, WFF failed to suppress NF-κB when A20 expression was silenced by siRNA.

CONCLUSION

WFF activated Nrf2 and expressed A20. Given that Nrf2 suppresses inflammation and A20 broadly disrupts inflammatory signaling cascades, our results suggest that the anti-inflammatory activity of WFF is attributable to Nrf2 and A20.

摘要

民族药理学相关性

连翘水提物(WFF)是一种草药疗法,用于治疗传统中药中的各种炎症性疾病。虽然已经报道了 WFF 的抗炎活性,但该活性的潜在机制尚不清楚。在这里,我们研究了 WFF 的抗炎活性是否与 Nrf2(一种抗炎因子)和 A20(一种抑制内毒素或细胞因子信号级联反应的泛素调节蛋白)有关。

材料和方法

制备并通过 HPLC 对连翘(Thunb.)Vahl 的水提取物进行指纹图谱分析。通过 MTT 和 FACS 分析分别测定 WFF 诱导的细胞毒性和细胞内 ROS。通过免疫印迹分析核蛋白和细胞质蛋白。通过半定量 RT-PCR 分析 mRNA 的表达。通过 Image J 定量分析蛋白质或基因的表达。

结果

WFF 激活了 Nrf2,诱导 RAW 264.7 细胞中 Nrf2 依赖性基因的表达,如 HO-1、NQO1 和 GCLC。另一方面,WFF 抑制了 LPS 或 TNF-α诱导的 NF-κB,这与 A20 的表达一致。相反,当 A20 的表达被 siRNA 沉默时,WFF 未能抑制 NF-κB。

结论

WFF 激活了 Nrf2 并表达了 A20。鉴于 Nrf2 抑制炎症,A20 广泛破坏炎症信号级联反应,我们的结果表明,WFF 的抗炎活性归因于 Nrf2 和 A20。

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