Liu Hai-Jiao, Pan Xiu-Xiu, Liu Bing-Qian, Gui Xuan, Hu Liang, Jiang Chun-Yi, Han Yuan, Fan Yi-Xin, Tang Yu-Lin, Liu Wen-Tao
Jiangsu Key Laboratory of Neurodegeneration, Department of Pharmacology, Nanjing Medical University, Nanjing, Jiangsu, 211166, People's Republic of China.
Department of Pharmacology, China Pharmaceutical University, Nanjing, Jiangsu, 211198, People's Republic of China.
J Neuroinflammation. 2017 Apr 4;14(1):74. doi: 10.1186/s12974-017-0849-y.
Gout is one of the common inflammatory arthritis which affects many people for inflicting unbearable pain. Macrophage-mediated inflammation plays an important role in gout. The uptake of monosodium urate (MSU) crystals by macrophages can lead to activation of NOD-like receptors containing a PYD 3 (NLRP3) inflammasome, thus accelerating interleukin (IL)-1β production. Reactive oxygen species (ROS) promoted development of the inflammatory process through NLRP3 inflammasome. Our study aimed to find a food-derived compound to attenuate gout pain via the specific inhibition of the NLRP3 inflammasome in macrophages.
CD-1 mice were used to evaluate the degree of pain and the swelling dimension of joints after an intra-articular (IA) MSU injection in the ankle. The murine macrophage cell line Raw 264.7 was used to investigate the effects of procyanidins and the mechanism underlying such effects. Histological analysis was used to measure the infiltration of inflammatory cells. ROS produced from Raw 264.7 cells were evaluated by flow cytometry. Cell signaling was measured by Western blot assay and immunofluorescence.
Procyanidins significantly attenuated gout pain and suppressed ankle swelling. Procyanidins also inhibited MSU-induced activation of the NLRP3 inflammasome and increase of IL-1β. Furthermore, procyanidins decreased ROS levels in Raw 264.7 cells.
Suppression of the NLRP3 inflammasome in macrophages contributes to the amelioration of gout pain by procyanidins.
痛风是一种常见的炎症性关节炎,许多人深受其带来的难以忍受的疼痛折磨。巨噬细胞介导的炎症在痛风中起重要作用。巨噬细胞摄取尿酸单钠(MSU)晶体可导致含PYD结构域的NOD样受体3(NLRP3)炎性小体激活,从而加速白细胞介素(IL)-1β的产生。活性氧(ROS)通过NLRP3炎性小体促进炎症过程的发展。我们的研究旨在寻找一种食物来源的化合物,通过特异性抑制巨噬细胞中的NLRP3炎性小体来减轻痛风疼痛。
使用CD-1小鼠评估踝关节内注射MSU后关节的疼痛程度和肿胀尺寸。使用小鼠巨噬细胞系Raw 264.7研究原花青素的作用及其潜在机制。组织学分析用于测量炎性细胞的浸润情况。通过流式细胞术评估Raw 264.7细胞产生的ROS。通过蛋白质印迹分析和免疫荧光测量细胞信号传导。
原花青素显著减轻痛风疼痛并抑制踝关节肿胀。原花青素还抑制MSU诱导的NLRP3炎性小体激活和IL-1β增加。此外,原花青素降低了Raw 264.7细胞中的ROS水平。
巨噬细胞中NLRP3炎性小体的抑制有助于原花青素改善痛风疼痛。