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苦参酮和去甲苦参酮抑制NLRP3炎性小体激活,并调节巨噬细胞极化以对抗溃疡性结肠炎。

Kurarinone and Nor-kurarinone inhibit NLRP3 inflammasome activation and regulate macrophage polarization against ulcerative colitis.

作者信息

Li Wanyu, Li Yadi, Qiu Yongyi, Huang Ruiting, Niu Jing, Chen Jiawen, Liu Yi, Chen Lei

机构信息

School of Traditional Chinese Medicine, Guangdong Pharmaceutical University, Guangzhou 510006, China.

School of Chinese Medicine, Southern Medical University, Guangzhou 510515, China.

出版信息

Int Immunopharmacol. 2025 Jun 5;157:114758. doi: 10.1016/j.intimp.2025.114758. Epub 2025 May 1.

Abstract

Activation of NOD-like receptor protein 3 (NLRP3) can lead to the production of inflammatory factors and perturbation of macrophage polarization, leading to an intestinal immune imbalance that promotes the progression of ulcerative colitis (UC). In this study, we investigated the therapeutic effect of Kurarinone and Nor-kurarinone on UC and their regulatory mechanisms relating to NLRP3 inflammasome activation and macrophage polarization. UC mice were induced using dextran sulfate sodium (DSS) and treated with Kurarinone and Nor-kurarinone. Results showed that Kurarinone and Nor-kurarinone could alleviate weight loss, decrease the disease activity index (DAI) score, shorten colon length, inhibit formation of the NLRP3 inflammasome in the colon and regulate macrophage polarization in UC mice. The THP-1 cells were used as an in vitro model of the NLRP3 inflammasome, conducted by treatment with lipopolysaccharide (LPS) and ATP/Nigericin. Kurarinone and Nor-kurarinone can inhibit the NLRP3 inflammasome formation response by disrupting the NLRP3/ASC interaction to inhibit NLRP3 assembly and then regulating the polarization of macrophages. In conclusion, Kurarinone and Nor-kurarinone inhibited NLRP3 inflammasome assembly to counteract activation of the NLRP3 inflammasome. This inhibition led to a reduction in M1 polarization of intestinal macrophages in UC mice to keep the balance of M1/ M2 macrophages. Our study suggests that Kurarinone and Nor-kurarinone may be novel therapeutic modalities for UC.

摘要

NOD样受体蛋白3(NLRP3)的激活可导致炎症因子的产生以及巨噬细胞极化的紊乱,进而导致肠道免疫失衡,促进溃疡性结肠炎(UC)的进展。在本研究中,我们探究了苦参酮和去甲苦参酮对UC的治疗作用及其与NLRP3炎性小体激活和巨噬细胞极化相关的调控机制。使用葡聚糖硫酸钠(DSS)诱导UC小鼠,并给予苦参酮和去甲苦参酮进行治疗。结果显示,苦参酮和去甲苦参酮可减轻体重减轻,降低疾病活动指数(DAI)评分,缩短结肠长度,抑制结肠中NLRP3炎性小体的形成,并调节UC小鼠的巨噬细胞极化。将THP-1细胞用作NLRP3炎性小体的体外模型,通过脂多糖(LPS)和ATP/尼日利亚菌素进行处理。苦参酮和去甲苦参酮可通过破坏NLRP3/凋亡相关斑点样蛋白(ASC)相互作用来抑制NLRP3炎性小体形成反应,从而抑制NLRP3组装,进而调节巨噬细胞极化。总之,苦参酮和去甲苦参酮抑制NLRP3炎性小体组装以对抗NLRP3炎性小体的激活。这种抑制导致UC小鼠肠道巨噬细胞的M1极化减少,以维持M1/M2巨噬细胞的平衡。我们的研究表明,苦参酮和去甲苦参酮可能是UC的新型治疗方式。

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