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水提取物通过 STAT/NF-κB 通路和 HO-1 表达调控病毒感染 RAW264.7 细胞的抗炎作用。

Anti-inflammatory effects of Water Extract are regulated by the STAT/NF-κB pathway and HO-1 expression in Virus-infected RAW264.7 cells.

机构信息

Department of Optometry, Asia University, Taichung, Taiwan.

Genetics Center, Department of Medical Research, China Medical University Hospital, and School of Chinese Medicine, China Medical University, Taichung, Taiwan.

出版信息

Int J Med Sci. 2021 Mar 30;18(11):2285-2293. doi: 10.7150/ijms.56198. eCollection 2021.

Abstract

This study examined the effect of the Flos Lonicerae Japonicae water extract (FLJWE), chlorogenic acid, and luteolin on pseudorabies virus (PRV)-induced inflammation in RAW264.7 cells and elucidated related molecular mechanisms. The results revealed that FLJWE and luteolin, but not chlorogenic acid, inhibited the production of inducible nitric oxide synthase (iNOS), cyclooxygenase-2 (COX-2), and inflammatory cytokines in PRV-infected RAW 264.7 cells. We found that the FLJWE and luteolin suppressed nuclear factor (NF)-κB activation by inhibiting the phosphorylation of signal transducer and activator of transcription 1 and 3 (STAT1 and STAT3, respectively). Moreover, the FLJWE significantly upregulated the expression of pNrf2 and its downstream target gene heme oxygenase-1 (HO-1). Our data indicated that FLJWE and luteolin reduced the expression of proinflammatory mediators and inflammatory cytokines, such as COX-2 and iNOS, through the suppression of the JAK/STAT1/3-dependent NF-κB pathway and the induction of HO-1 expression in PRV-infected RAW264.7 cells. The findings indicate that the FLJWE can be used as a potential antiviral agent.

摘要

本研究探讨了金银花水提取物(FLJWE)、绿原酸和木犀草素对 PRV 诱导的 RAW264.7 细胞炎症的影响,并阐明了相关的分子机制。结果表明,FLJWE 和木犀草素,但不是绿原酸,抑制了 PRV 感染的 RAW264.7 细胞中诱导型一氧化氮合酶(iNOS)、环氧化酶-2(COX-2)和炎症细胞因子的产生。我们发现,FLJWE 和木犀草素通过抑制信号转导和转录激活因子 1 和 3(分别为 STAT1 和 STAT3)的磷酸化来抑制核因子(NF)-κB 的激活。此外,FLJWE 显著上调了 pNrf2 及其下游靶基因血红素加氧酶-1(HO-1)的表达。我们的数据表明,FLJWE 和木犀草素通过抑制 JAK/STAT1/3 依赖性 NF-κB 通路和诱导 PRV 感染的 RAW264.7 细胞中 HO-1 的表达,降低了促炎介质和炎症细胞因子(如 COX-2 和 iNOS)的表达。这些发现表明,FLJWE 可用作一种潜在的抗病毒药物。

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