Ma Zhenyuan, Huang Zhengquan, Zhang Li, Li Xiaochen, Xu Bo, Xiao Yancheng, Shi Xiaoqing, Zhang Haosheng, Liao Taiyang, Wang Peimin
Department of Orthopedics, Affiliated Hospital of Nanjing University of Chinese Medicine, Nanjing, China.
Jiangsu Province Hospital of Chinese Medicine, Nanjing, China.
Front Pharmacol. 2021 Feb 15;11:599022. doi: 10.3389/fphar.2020.599022. eCollection 2020.
: Synovitis plays an important role in knee osteoarthritis (KOA) pain. The activation of the NOD-like receptor protein 3 (NLRP3) inflammasome in fibroblast-like synoviocytes (FLSs) promotes KOA development. In this study, we aimed to investigate whether vanillic acid (VA), a monomer derived from Chinese herbal medicines, could target NLRP3 inflammasome-related synovitis to reduce pain. : Rats in the KOA and KOA + VA groups were injected with monosodium iodoacetate (MIA) in the knee to induce KOA. From day 14, the KOA + VA group was given VA at 30 mg/kg every day via gastric intubation. FLSs were collected from the synovial tissues. We examined both the protein and gene expression of caspase-1, apoptosis-associated speck-like protein with a caspase recruitment domain (ASC), NLRP3, components of the NLRP3 inflammasome, and interleukin-1β (IL-1β) and IL-18 and . : The upregulation of caspase-1, ASC, and NLRP3 in the KOA model were reduced by VA. VA also lowered the level of IL-1β and IL-18 in the KOA model. In addition, VA relieved pain-related behavior of KOA model rats and downregulated the pain mediators CGRP, NGF, and TrkA in FLSs. Interestingly, we also observed reduced synovial fibrosis in the animal experiments. : Our research showed that VA reduces synovitis and pain-related behaviors in a rat model of KOA, which provides the basis for further investigations into the potential therapeutic impact of VA in KOA.
滑膜炎在膝关节骨关节炎(KOA)疼痛中起重要作用。成纤维样滑膜细胞(FLS)中NOD样受体蛋白3(NLRP3)炎性小体的激活促进KOA的发展。在本研究中,我们旨在研究源自中草药的单体香草酸(VA)是否可以靶向NLRP3炎性小体相关的滑膜炎以减轻疼痛。:KOA组和KOA + VA组大鼠膝关节注射碘乙酸钠(MIA)诱导KOA。从第14天起,KOA + VA组每天经胃管给予30 mg/kg的VA。从滑膜组织中收集FLS。我们检测了半胱天冬酶-1、含半胱天冬酶募集结构域的凋亡相关斑点样蛋白(ASC)、NLRP3、NLRP3炎性小体的成分、白细胞介素-1β(IL-1β)和IL-18的蛋白质和基因表达。:VA降低了KOA模型中半胱天冬酶-1、ASC和NLRP3的上调。VA还降低了KOA模型中IL-1β和IL-18的水平。此外,VA减轻了KOA模型大鼠的疼痛相关行为,并下调了FLS中疼痛介质降钙素基因相关肽(CGRP)、神经生长因子(NGF)和酪氨酸激酶A(TrkA)。有趣的是,我们在动物实验中还观察到滑膜纤维化减轻。:我们的研究表明,VA可减轻KOA大鼠模型中的滑膜炎和疼痛相关行为,这为进一步研究VA在KOA中的潜在治疗作用提供了基础。