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来自海洋海绵的异沙蚕酮通过抑制RAW 264.7巨噬细胞中的5-脂氧合酶/核因子κB/丝裂原活化蛋白激酶以及上调核因子E2相关因子2/血红素加氧酶-1来减轻活性氧和炎症。

Dysiarenone from Marine Sponge Attenuates ROS and Inflammation via Inhibition of 5-LOX/NF-κB/MAPKs and Upregulation of Nrf-2/OH-1 in RAW 264.7 Macrophages.

作者信息

Hu Tian-Yong, Zhang Hua, Chen Yan-Yan, Jiao Wei-Hua, Fan Jun-Ting, Liu Zhi-Qiang, Lin Hou-Wen, Cheng Bao-Hui

机构信息

Shenzhen Key Laboratory of ENT, Institute of ENT and Longgang ENT Hospital, Shenzhen, 518172, People's Republic of China.

Research Center for Marine Drugs, State Key Laboratory of Oncogene and Related Genes, Department of Pharmacy, Ren Ji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, 200127, People's Republic of China.

出版信息

J Inflamm Res. 2021 Feb 25;14:587-597. doi: 10.2147/JIR.S283745. eCollection 2021.

Abstract

BACKGROUND

Marine natural products harbor a variety of pharmacological activities, and the sea species have been becoming a main source of new drug candidate. In pursuit of safer and more effective anti-inflammation drug, the anti-inflammatory activities, anti-oxygenation effects and underlying molecular mechanisms of compound dysiarenone from were investigated via LPS-induced RAW 264.7 cell model.

METHODS

Firstly, RAW 264.7 cells have been stimulated with LPS and treated with dysiarenone, and the cell viability of the LPS-treated RAW 264.7 cells was examined. One-step method, DCFH-DA fluorescence probe method was used to detect reactive oxygen species (ROS). The modulation of dysiarenone on anti-inflammation was detected by enzyme-linked immunosorbent assay by measuring the release of inflammatory cytokines (TNF-α and IL-6), and inflammatory mediators (LTB4). Further, the underlying anti-inflammatory mechanism of dysiarenone was explored by determining the expression of inducible 5-LOX, MAPKs, p-Akt, and p-NF-κB p65. Oxidative stress is tightly connected with inflammation, which was also evaluated through nuclear factor erythroid 2-related factor 2 (Nrf2)/heme oxygenase-1 (OH-1) signaling pathway.

RESULTS

Our study unraveled that dysiarenone between 2 and 8 µM reduces the inflammation responses via suppressing the production of inflammatory cytokines (TNF-α and IL-6) and inflammatory mediators (LTB). Dysiarenone down-regulated the protein levels of inducible 5-LOX via the inhibition of phosphorylation of MAPKs (including p38, ERK), Akt and NF-κB p65. Additionally, dysiarenone decreases ROS accumulation by upregulating HO-1 expression via nuclear translocation of Nrf2.

CONCLUSION

In conclusion, we demonstrated that dysiarenone possesses anti-inflammation and anti-oxidation activity via inhibiting 5-LOX/NF-κB/MAPK and Nrf2/HO-1 signaling pathway. Dysiarenone might be a promising lead compound for inflammatory diseases.

摘要

背景

海洋天然产物具有多种药理活性,海洋物种已成为新药候选物的主要来源。为了寻找更安全、更有效的抗炎药物,通过脂多糖(LPS)诱导的RAW 264.7细胞模型,研究了化合物dysiarenone的抗炎活性、抗氧化作用及潜在的分子机制。

方法

首先,用LPS刺激RAW 264.7细胞并用dysiarenone处理,检测LPS处理的RAW 264.7细胞的细胞活力。采用一步法、DCFH-DA荧光探针法检测活性氧(ROS)。通过酶联免疫吸附测定法检测dysiarenone对炎症因子(TNF-α和IL-6)及炎症介质(LTB4)释放的影响,以检测其抗炎作用。此外,通过测定诱导型5-脂氧合酶(5-LOX)、丝裂原活化蛋白激酶(MAPKs)、磷酸化Akt(p-Akt)和磷酸化核因子κB p65(p-NF-κB p65)的表达,探索dysiarenone潜在的抗炎机制。氧化应激与炎症密切相关,也通过核因子红细胞2相关因子2(Nrf2)/血红素加氧酶-1(HO-1)信号通路进行评估。

结果

我们的研究表明,2至8 μM的dysiarenone通过抑制炎症因子(TNF-α和IL-6)及炎症介质(LTB)的产生来减轻炎症反应。Dysiarenone通过抑制MAPKs(包括p38、ERK)、Akt和NF-κB p65的磷酸化,下调诱导型5-LOX的蛋白水平。此外,dysiarenone通过Nrf2的核转位上调HO-1的表达,从而减少ROS的积累。

结论

总之,我们证明dysiarenone通过抑制5-LOX/NF-κB/MAPK和Nrf2/HO-1信号通路具有抗炎和抗氧化活性。Dysiarenone可能是一种有前途的治疗炎症性疾病的先导化合物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/50c8/7921866/1c054e78821c/JIR-14-587-g0001.jpg

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