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8-姜酚通过靶向 TAK1 抑制类风湿性关节炎。

8-Shogaol inhibits rheumatoid arthritis through targeting TAK1.

机构信息

Department of Biotechnology, Yonsei University, Seoul 03722, Republic of Korea.

Immunopathology Lab, School of Bio Sciences and Technology, Vellore Institute of Technology (VIT), Vellore 632 014, Tamil Nadu, India.

出版信息

Pharmacol Res. 2022 Apr;178:106176. doi: 10.1016/j.phrs.2022.106176. Epub 2022 Mar 10.

Abstract

Rheumatoid arthritis (RA) is a chronic immune-mediated disorder, mainly characterized by synovial inflammation and joint damage. If insufficiently treated, RA can lead to irreversible joint destruction and decreased life expectancy. While better understanding of the pathologies and the development of new antirheumatic drugs have improved the outcome of individuals with RA, many patients still cannot achieve remission and experience progressive disability. Fibroblast-like synoviocytes (FLS) have gained attention due to its pivotal role in RA pathogenesis and thus targeting FLS has been suggested as an attractive therapeutic strategy. To identify candidate molecules with strong inhibitory activity against FLS inflammation, we tested the effect of 315 natural extracts against IL-17-mediated IL-6 production. Zingiber officinale was found as the top hit and further analysis on the active compound responsible led to the discovery of 8-shogaol as a potent molecule against synovitis. 8-Shogaol displayed significant inhibitory effects against TNF-α-, IL-1β-, and IL-17-mediated inflammation and migration in RA patient-derived FLS (RA-FLS) and 3D synovial culture system. 8-Shogaol selectively and directly inhibited TAK1 activity and subsequently suppressed IKK, Akt, and MAPK signaling pathways. Moreover, treatment with 8-shogaol reduced paw thickness and improved walking performance in the adjuvant-induced arthritic (AIA) rat model. 8-Shogaol also reversed pathologies of joint structure in AIA rats and decreased inflammatory biomarkers in the joints. Collectively, we report a novel natural compound that inhibits RA through reversing pathologies of the inflamed synovium via targeting TAK1.

摘要

类风湿关节炎(RA)是一种慢性免疫介导的疾病,主要特征为滑膜炎症和关节损伤。如果治疗不充分,RA 可导致不可逆的关节破坏和预期寿命缩短。尽管对病理的更好理解和新型抗风湿药物的开发改善了 RA 患者的预后,但许多患者仍无法达到缓解并经历进行性残疾。成纤维样滑膜细胞(FLS)因其在 RA 发病机制中的关键作用而受到关注,因此靶向 FLS 已被提议作为一种有吸引力的治疗策略。为了鉴定对 FLS 炎症具有强抑制活性的候选分子,我们测试了 315 种天然提取物对 IL-17 介导的 IL-6 产生的影响。姜黄被发现是顶级命中物,对负责的活性化合物的进一步分析导致发现 8-姜酚是一种针对滑膜炎的有效分子。8-姜酚对 TNF-α、IL-1β 和 IL-17 介导的 RA 患者来源的 FLS(RA-FLS)和 3D 滑膜培养系统中的炎症和迁移显示出显著的抑制作用。8-姜酚选择性且直接抑制 TAK1 活性,随后抑制 IKK、Akt 和 MAPK 信号通路。此外,8-姜酚治疗可减少佐剂诱导的关节炎(AIA)大鼠模型中的爪厚和改善行走性能。8-姜酚还可逆转 AIA 大鼠关节结构的病理学并降低关节中的炎症生物标志物。总之,我们报告了一种新型天然化合物,通过靶向 TAK1 抑制 RA,从而逆转发炎滑膜的病理。

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