Department of Biochemistry and Molecular Biology, Research Center for Infectious Diseases, School of Basic Medical Sciences, Anhui Medical University, Hefei, 230032, China; Provincial Key Laboratory of Zoonoses of High Institutions in Anhui, Anhui Medical University, Hefei, 230032, China.
Center for Scientific Research of Anhui Medical University, Anhui Medical University, Hefei, 230032, China.
Eur J Pharmacol. 2023 Dec 5;960:176149. doi: 10.1016/j.ejphar.2023.176149. Epub 2023 Oct 21.
Macrophages present strong immunomodulatory ability and are considered to be core immune cells in the process of hepatic ischaemia‒reperfusion (I/R). The NLRP3 inflammasome is a kind of intracellular multimolecular complex that actively participates in innate immune responses and proinflammatory signalling pathways. Piceatannol (PIC) is a derivative of the natural phenolic compound resveratrol and has antioxidant and anti-inflammatory effects. The purpose of this study was to examine whether pretreatment with PIC can alleviate hepatic I/R injury by targeting NLRP3 inflammasome-induced macrophage pyroptosis.
PIC-pretreated primary hepatic macrophages were subjected to hypoxia/reoxygenation, and liver ischaemia/reperfusion was performed in mice.
PIC pretreatment ameliorated histopathological changes, oxidative stress and inflammation while enhancing antioxidant and anti-inflammasome markers through downregulation of Toll-like receptor 4 (TLR4), p-IκBα (S32), p-NF-κBp65 (S536), NLRP3, caspase-1 (p20), IL-1β, IL-18 and GSDMD-N expression during liver ischaemia‒reperfusion. Moreover, PIC inhibited the translocation of NF-κB p65 after stimulation with hypoxia/reoxygenation in primary hepatic macrophages.
The results indicated that PIC protected the liver against hepatic I/R injury, which was mediated by targeting TLR4-NF-κB-NLRP3-mediated hepatic macrophage pyroptosis.
巨噬细胞具有很强的免疫调节能力,被认为是肝缺血再灌注(I/R)过程中的核心免疫细胞。NLRP3 炎性体是一种细胞内多分子复合物,积极参与固有免疫反应和促炎信号通路。白藜芦醇(PIC)是天然多酚化合物白藜芦醇的衍生物,具有抗氧化和抗炎作用。本研究旨在探讨 PIC 是否可以通过靶向 NLRP3 炎性体诱导的巨噬细胞焦亡来减轻肝 I/R 损伤。
用 PIC 预处理原代肝巨噬细胞,进行缺氧/复氧,然后在小鼠中进行肝缺血/再灌注。
PIC 预处理通过下调 Toll 样受体 4(TLR4)、p-IκBα(S32)、p-NF-κBp65(S536)、NLRP3、caspase-1(p20)、IL-1β、IL-18 和 GSDMD-N 的表达,改善了肝缺血再灌注时的组织病理学变化、氧化应激和炎症,同时增强了抗氧化和抗炎性体标志物。此外,PIC 抑制了缺氧/复氧刺激后原代肝巨噬细胞中 NF-κB p65 的易位。
结果表明,PIC 通过靶向 TLR4-NF-κB-NLRP3 介导的肝巨噬细胞焦亡,保护肝脏免受肝 I/R 损伤。