Department of Pharmacy, The First Affiliated Hospital of Anhui Medical University, Hefei, China.
The Grade 3 Pharmaceutical Chemistry Laboratory, State Administration of Traditional Chinese Medicine, Hefei, China.
Front Immunol. 2023 Mar 27;14:1137822. doi: 10.3389/fimmu.2023.1137822. eCollection 2023.
Gout arthritis (GA) is a common and curable type of inflammatory arthritis that has been attributed to a combination of genetic, environmental and metabolic factors. Chronic deposition of monosodium urate (MSU) crystals in articular and periarticular spaces as well as subsequent activation of innate immune system in the condition of persistent hyperuricemia are the core mechanisms of GA. As is well known, drugs for GA therapy primarily consists of rapidly acting anti-inflammatory agents and life-long uric acid lowering agents, and their therapeutic outcomes are far from satisfactory. Although MSU crystals in articular cartilage detected by arthrosonography or in synovial fluid found by polarization microscopy are conclusive proofs for GA, the exact molecular mechanism of NLRP3 inflammasome activation in the course of GA still remains mysterious, severely restricting the early diagnosis and therapy of GA. On the one hand, the activation of Nod-like receptor family, pyrin domain containing 3 (NLRP3) inflammasome requires nuclear factor kappa B (NF-κB)-dependent transcriptional enhancement of NLRP3, precursor (pro)-caspase-1 and pro-IL-1β, as well as the assembly of NLRP3 inflammasome complex and sustained release of inflammatory mediators and cytokines such as IL-1β, IL-18 and caspase-1. On the other hand, NLRP3 inflammasome activated by MSU crystals is particularly relevant to the initiation and progression of GA, and thus may represent a prospective diagnostic biomarker and therapeutic target. As a result, pharmacological inhibition of the assembly and activation of NLRP3 inflammasome may also be a promising avenue for GA therapy. Herein, we first introduced the functional role of NLRP3 inflammasome activation and relevant biological mechanisms in GA based on currently available evidence. Then, we systematically reviewed therapeutic strategies for targeting NLRP3 by potentially effective agents such as natural products, novel compounds and noncoding RNAs (ncRNAs) in the treatment of MSU-induced GA mouse models. In conclusion, our present review may have significant implications for the pathogenesis, diagnosis and therapy of GA.
痛风性关节炎(GA)是一种常见且可治愈的炎性关节炎,其发生归因于遗传、环境和代谢因素的综合作用。在持续性高尿酸血症的情况下,单钠尿酸盐(MSU)晶体在关节和关节周围空间中的慢性沉积以及随后固有免疫系统的激活是 GA 的核心机制。众所周知,GA 治疗药物主要包括快速作用的抗炎药和终身降尿酸药,但它们的治疗效果远不理想。尽管关节软骨中通过关节超声或偏振显微镜在滑液中检测到的 MSU 晶体是 GA 的确凿证据,但 NLRP3 炎性体在 GA 过程中激活的确切分子机制仍不清楚,这严重限制了 GA 的早期诊断和治疗。一方面,Nod 样受体家族、含 pyrin 域蛋白 3(NLRP3)炎性体的激活需要核因子 kappa B(NF-κB)依赖性 NLRP3、前体(pro)-胱冬肽酶-1 和 pro-IL-1β转录增强,以及 NLRP3 炎性体复合物的组装和炎症介质和细胞因子(如 IL-1β、IL-18 和胱冬肽酶-1)的持续释放。另一方面,MSU 晶体激活的 NLRP3 炎性体与 GA 的发生和进展特别相关,因此可能代表有前途的诊断生物标志物和治疗靶点。因此,抑制 NLRP3 炎性体的组装和激活也可能是 GA 治疗的一种有前途的方法。在此,我们首先根据现有证据介绍了 NLRP3 炎性体激活及其在 GA 中的相关生物学机制的功能作用。然后,我们系统地综述了针对 NLRP3 的治疗策略,包括天然产物、新型化合物和非编码 RNA(ncRNA)等潜在有效药物在 MSU 诱导的 GA 小鼠模型中的治疗作用。总之,本综述可能对 GA 的发病机制、诊断和治疗具有重要意义。