Frontiers in Pharmacology (Feb 2021)

Vanillic Acid Reduces Pain-Related Behavior in Knee Osteoarthritis Rats Through the Inhibition of NLRP3 Inflammasome-Related Synovitis

  • Zhenyuan Ma,
  • Zhenyuan Ma,
  • Zhenyuan Ma,
  • Zhengquan Huang,
  • Zhengquan Huang,
  • Li Zhang,
  • Li Zhang,
  • Li Zhang,
  • Xiaochen Li,
  • Xiaochen Li,
  • Xiaochen Li,
  • Bo Xu,
  • Bo Xu,
  • Bo Xu,
  • Yancheng Xiao,
  • Yancheng Xiao,
  • Yancheng Xiao,
  • Xiaoqing Shi,
  • Xiaoqing Shi,
  • Haosheng Zhang,
  • Haosheng Zhang,
  • Haosheng Zhang,
  • Taiyang Liao,
  • Taiyang Liao,
  • Taiyang Liao,
  • Peimin Wang,
  • Peimin Wang

DOI
https://doi.org/10.3389/fphar.2020.599022
Journal volume & issue
Vol. 11

Abstract

Read online

Objectives: 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.Methods: 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 in vivo and in vitro.Results: 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.Conclusion: 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.

Keywords