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LMT-28 与山奈酚联合治疗胶原诱导关节炎模型的抗炎作用。

Anti-inflammatory effect of the combined treatment of LMT-28 and kaempferol in a collagen-induced arthritis mouse model.

机构信息

Laboratory of Pharmacoimmunology, Integrated Research Institute of Pharmaceutical Sciences and BK21 FOUR Team for Advanced Program for Smart Pharma Leaders, College of Pharmacy, The Catholic University of Korea, Bucheon-si, Gyeonggi-do, Republic of Korea.

Biowave, Anyangcheon-ro, Yangcheon-gu, Seoul, Republic of Korea.

出版信息

PLoS One. 2024 Jul 31;19(7):e0302119. doi: 10.1371/journal.pone.0302119. eCollection 2024.

Abstract

Rheumatoid arthritis (RA) is an autoimmune disease characterized by joint inflammation and swelling. Several studies have demonstrated that RA fibroblast-like synovial cells (RA-FLS) play an important role in RA pathogenesis. Activated RA-FLS contribute to synovial inflammation by secreting inflammatory cytokines including interleukin (IL)-1β, IL-6 and tumor necrosis factor-α. LMT-28 is derivative of oxazolidone and exerts anti-inflammatory effects on RA via IL-6 signaling pathway regulation. LMT-28 also regulates T cell differentiation in RA condition. However, the effect of LMT-28 on the migration and invasion of RA-FLS remains unknown. Kaempferol has been reported to have pharmacological effects on various diseases, such as inflammatory diseases, autoimmune diseases, and cancer. Additionally, kaempferol has been reported to inhibit RA-FLS migration and invasion, but it is not known about the therapeutic mechanism including molecular mechanism such as receptor. The present study aimed to investigate the synergistic effects of the combined treatment of LMT-28 and kaempferol on RA-FLS activation and RA pathogenesis in mouse model. LMT-28 and kaempferol co-administration inhibited RA disease severity and histological collapse in the joint tissues of CIA mice, as well as downregulated the levels of pro-inflammatory cytokines in mouse serum. Additionally, the combined treatment inhibited excessive differentiation of T helper 17 cells and osteoclasts. Furthermore, compared with single treatments, combined treatment showed enhanced inhibitory effects on the hyperactivation of IL-6-induced signaling pathway in RA-FLS. Combined treatment also inhibited RA-FLS cell proliferation, migration, and invasion and suppressed the expression of matrix metalloproteinase in RA-FLS. Furthermore, we confirmed that the combined treatment inhibited chondrocyte proliferation, migration, and invasion. In conclusion, our results suggest that the combined treatment of LMT-28 and kaempferol exerts a synergistic effect on the RA development via the regulation of IL-6-induced hyperactivation of RA-FLS. Furthermore, this study suggests that combination therapies can be an effective therapeutic option for arthritis.

摘要

类风湿关节炎(RA)是一种以关节炎症和肿胀为特征的自身免疫性疾病。多项研究表明,RA 成纤维样滑膜细胞(RA-FLS)在 RA 发病机制中起重要作用。激活的 RA-FLS 通过分泌包括白细胞介素(IL)-1β、IL-6 和肿瘤坏死因子-α在内的炎症细胞因子促进滑膜炎症。LMT-28 是恶唑烷酮的衍生物,通过调节 IL-6 信号通路发挥对 RA 的抗炎作用。LMT-28 还调节 RA 条件下 T 细胞分化。然而,LMT-28 对 RA-FLS 的迁移和侵袭的影响尚不清楚。山奈酚已被报道在各种疾病中具有药理作用,如炎症性疾病、自身免疫性疾病和癌症。此外,山奈酚已被报道抑制 RA-FLS 的迁移和侵袭,但关于其治疗机制,包括受体等分子机制,尚不清楚。本研究旨在探讨 LMT-28 和山奈酚联合治疗对 CIA 小鼠模型中 RA-FLS 激活和 RA 发病机制的协同作用。LMT-28 和山奈酚联合治疗抑制 CIA 小鼠关节组织中 RA 疾病的严重程度和组织学破坏,并下调小鼠血清中促炎细胞因子的水平。此外,联合治疗抑制了 Th17 细胞和破骨细胞的过度分化。此外,与单一治疗相比,联合治疗对 RA-FLS 中 IL-6 诱导的信号通路的过度激活表现出更强的抑制作用。联合治疗还抑制了 RA-FLS 细胞的增殖、迁移和侵袭,并抑制了 RA-FLS 中基质金属蛋白酶的表达。此外,我们证实联合治疗抑制了软骨细胞的增殖、迁移和侵袭。总之,我们的研究结果表明,LMT-28 和山奈酚的联合治疗通过调节 RA-FLS 中 IL-6 诱导的过度激活对 RA 的发展发挥协同作用。此外,本研究表明联合治疗可能是关节炎的一种有效治疗选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fbd0/11290667/227eb4f1f478/pone.0302119.g001.jpg

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