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活血通络方对中性粒细胞胞外诱捕网形成的影响及作用机制

Effects and Action Mechanism of Huoxue Tongluo Formula on the Formation of Neutrophil Extracellular Traps.

作者信息

Zhou Xiaoli, Liao Weixiang, Peng Wei, Xie Tingting, Yin Qianlu, Zheng Yuhang

机构信息

Department of Peripheral Vascular (Wound Repair), Chongqing Hospital of Traditional Chinese Medicine, Chongqing 400021, China.

Graduate School, Guizhou University of Traditional Chinese Medicine, Guiyang 550002, China.

出版信息

Evid Based Complement Alternat Med. 2022 Aug 18;2022:1240967. doi: 10.1155/2022/1240967. eCollection 2022.

Abstract

Excessive infiltration and uncontrolled activation of neutrophil extracellular traps (NETs) are likely to destroy normal tissue architecture and cause uncontrolled inflammation. The present research attempted to screen potential signaling pathways of Huoxue Tongluo Formula (HXTLF) affecting the formation of NETs using network pharmacology technique. Active chemical components of HXTLF and therapeutic targets related to vasculitis were screened, and a chemical components-targets network diagram of HXTLF was constructed by Cytoscape. Finally, the inhibitory effect and mechanism of HXTLF on the formation of NETs were explored in vitro using LPS-induced NETs. Immunofluorescence and Western blot were conducted to determine the protein fluorescence intensity and relative expression. The experimental results illustrated that HXTLF mediated the expression levels of H3Cit and myeloperoxidase (MPO) protein in neutrophils activated by LPS, inhibited NETs formation, and reduced the concentration of interleukin- (IL-) 1, a proinflammatory factor in cells. Additionally, we activated and inhibited the AKT1 signaling pathway using the corresponding activator and inhibitor to explore the regulatory mechanism of HXTLF on AKT1 and other molecules in the treatment of vasculitis. The results demonstrated that HXTLF could inhibit the phosphorylation of AKT1, IKK, and NF-B proteins, inhibit NETs formation, and reduce IL-1 concentration, indicating that AKT1 exerts a vital role in the treatment of vasculitis after HXTLF administration. The current study initially revealed the pharmacological mechanism of HXTLF for vasculitis management using network pharmacology techniques and tests in vitro, which is expected to provide important theoretical basis for elucidating the molecular mechanism of HXTLF and promoting its clinical application.

摘要

中性粒细胞胞外诱捕网(NETs)的过度浸润和失控激活可能会破坏正常组织结构并导致失控性炎症。本研究试图运用网络药理学技术筛选活血通络方(HXTLF)影响NETs形成的潜在信号通路。筛选了HXTLF的活性化学成分以及与血管炎相关的治疗靶点,并通过Cytoscape构建了HXTLF的化学成分-靶点网络图。最后,在体外利用脂多糖(LPS)诱导的NETs探讨HXTLF对NETs形成的抑制作用及其机制。进行免疫荧光和蛋白质印迹法以测定蛋白质荧光强度和相对表达量。实验结果表明,HXTLF介导了LPS激活的中性粒细胞中组蛋白H3瓜氨酸化(H3Cit)和髓过氧化物酶(MPO)蛋白的表达水平,抑制了NETs的形成,并降低了细胞中促炎因子白细胞介素-1(IL-1)的浓度。此外,我们使用相应的激活剂和抑制剂激活并抑制AKT1信号通路,以探讨HXTLF在治疗血管炎中对AKT1及其他分子的调控机制。结果表明,HXTLF可抑制AKT1、IKK和NF-κB蛋白的磷酸化,抑制NETs形成,并降低IL-1浓度,表明AKT1在给予HXTLF后治疗血管炎中发挥着重要作用。本研究初步揭示了HXTLF运用网络药理学技术和体外实验治疗血管炎的药理机制,有望为阐明HXTLF的分子机制并促进其临床应用提供重要的理论依据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a44f/9410787/12f9f9ed69fe/ECAM2022-1240967.001.jpg

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