State Key Laboratory of Quality Research in Chinese Medicine, Institute of Chinese Medical Sciences, University of Macau, Macao, China.
Br J Pharmacol. 2022 May;179(9):1978-1997. doi: 10.1111/bph.15773. Epub 2022 Jan 6.
Macrophage infiltration and activation is a critical step during acute colitis. Redox-mediated activation of NLRP3 inflammasomes in macrophages plays a critical role in mediating colonic inflammatory responses. Rhein isolated from the rhizome of rhubarb exhibits anti-inflammatory effects in various diseases. However, its role in regulating acute colonic inflammation is unexplored. Here, we investigated the protective mechanisms of rhein during acute gut inflammation and its regulation of macrophage activation.
Inhibitory effects of rhein on NLRP3 inflammasomes were evaluated in activated macrophages and a mouse model of colitis. Expression of inflammatory mediators, inflammasome complex and redox-related signalling were analysed by ELISA, Western blots, immunofluorescence staining, and qRT-PCR. The phenotype of macrophages was assessed by flow cytometry. Colonic inflammation was evaluated by histological analysis.
Rhein significantly decreased IL-1β secretion via NLRP3 inflammasomes by disturbing their assembly in macrophages. Rhein also activated the Nrf2-HO1-NQO1 pathway and inhibited expression of Nox2 subunits and translocation to regulate redox balance. Moreover, rhein attenuated inflammatory responses by mediating macrophage polarization from M1 to M2 phenotype. NF-κB, AP-1, and MAPK signalling were also involved in improving inflammatory conditions by rhein. In mice with acute intestinal inflammation, rhein treatment attenuated clinical features and reduced macrophage infiltration into damaged tissue to alleviate colonic inflammation.
Rhein regulated redox-mediated NLRP3 inflammasome activation to protect against acute colitis, by interfering with macrophage accumulation and polarization. These findings provide a promising strategy of novel compounds for regulating mucosal inflammation in gastrointestinal disorders.
巨噬细胞浸润和激活是急性结肠炎的关键步骤。氧化还原介导的巨噬细胞中 NLRP3 炎性小体的激活在介导结肠炎症反应中起着关键作用。大黄素是从大黄根茎中分离出来的,在各种疾病中表现出抗炎作用。然而,其在调节急性结肠炎症中的作用尚未被探索。在这里,我们研究了大黄素在急性肠道炎症中的保护机制及其对巨噬细胞激活的调节作用。
在活化的巨噬细胞和结肠炎小鼠模型中评估大黄素对 NLRP3 炎性小体的抑制作用。通过 ELISA、Western blot、免疫荧光染色和 qRT-PCR 分析炎症介质、炎性小体复合物和氧化还原相关信号的表达。通过流式细胞术评估巨噬细胞的表型。通过组织学分析评估结肠炎症。
大黄素通过干扰巨噬细胞中 NLRP3 炎性小体的组装,显著降低了 IL-1β 的分泌。大黄素还激活了 Nrf2-HO1-NQO1 途径,抑制了 Nox2 亚基的表达和易位,以调节氧化还原平衡。此外,大黄素通过介导巨噬细胞从 M1 向 M2 表型极化来减轻炎症反应。NF-κB、AP-1 和 MAPK 信号通路也参与了大黄素改善炎症状况。在急性肠道炎症的小鼠中,大黄素治疗减轻了临床特征,并减少了巨噬细胞浸润到受损组织中,从而缓解了结肠炎症。
大黄素通过干扰巨噬细胞的积累和极化来调节氧化还原介导的 NLRP3 炎性小体的激活,从而保护急性结肠炎。这些发现为调节胃肠道疾病黏膜炎症提供了一种有前途的新化合物策略。