Department of Pharmacology, College of Pharmacy, University of Sargodha, Sargodha, 40100, Pakistan.
Institute of Pharmacy, Lahore College for Women University, Lahore, Pakistan.
Inflammopharmacology. 2024 Aug;32(4):2445-2462. doi: 10.1007/s10787-024-01512-0. Epub 2024 Jun 25.
An immunologic system attacking the body's own tissues is a hallmark of autoimmune disorders, which encompass a wide range of unique conditions. Numerous essential biologic functions, including the regulation of the immune system, inflammation, cell division, and tissue repair, are carried out by cytokines. Natural compounds are an effective treatment for autoimmune illnesses by modulation of inflammatory cytokines and infiltration of leukocytes into the inflamed tissue. Here, anti-arthritic study was carried out using oral administration of Azelaic acid (AzA) for 28 days with doses (20, 40, and 80 mg/kg) in Complete Freund's Adjuvant (CFA) induced arthritis model. AzA ameliorated the adjuvant-induced arthritis by decreasing arthritic score, paw volume, improved body-weight alterations and serum levels of PGE2, 5-LOX and anti-ccp. AzA showed significant down regulation of NF-κB, COX-II, TNF-α, IL-17, IL-1β, IL-6, and up regulation of IL4 and IL10. Hemoglobin and RBCs count remarkably increased and ESR, CRP, platelets, WBCs levels markedly reduced in post treatment. In addition, the weakened SOD (superoxide dismutase), Catalase (CAT), Glutathione (GSH) activity and the increased levels of malondialdehyde (MDA) were all reversed by AzA treatment. And showed improved radiographical and histologic alterations in the structure of the joints. Molecular docking studies targeting COX-II, iNOS, TNF-α, 5-LOX, IL4, IL10, IL-6, and IL-17 establish a correlation between theoretical and experimental results. Results showed that AzA inhibit pro-inflammatory cytokines (COX-II, TNF-α, 5-LOX, IL-17, NF-κB, IL-1β, and IL-6) and increase anti-inflammatory cytokines, which supported the anti-arthritic and immunomodulatory potential of AzA.
自身免疫性疾病的一个标志是免疫系统攻击身体自身的组织,它包含了广泛的独特病症。细胞因子在许多重要的生物学功能中发挥作用,包括免疫系统的调节、炎症、细胞分裂和组织修复。天然化合物通过调节炎症细胞因子和白细胞浸润到炎症组织中,是治疗自身免疫性疾病的有效方法。在这里,通过用 28 天的剂量(20、40 和 80mg/kg)口服壬二酸(AzA)进行抗关节炎研究,在完全弗氏佐剂(CFA)诱导的关节炎模型中。AzA 通过降低关节炎评分、爪子体积、改善体重变化以及血清 PGE2、5-LOX 和抗-ccp 水平来改善佐剂诱导的关节炎。AzA 显示 NF-κB、COX-II、TNF-α、IL-17、IL-1β、IL-6 的显著下调,以及 IL4 和 IL10 的显著上调。治疗后血红蛋白和红细胞计数显著增加,ESR、CRP、血小板、白细胞计数显著降低。此外,AzA 治疗还能逆转 SOD(超氧化物歧化酶)、CAT(过氧化氢酶)、GSH(谷胱甘肽)活性的减弱以及 MDA(丙二醛)水平的升高。并显示出关节结构的放射学和组织学改变得到改善。针对 COX-II、iNOS、TNF-α、5-LOX、IL4、IL10、IL-6 和 IL-17 的分子对接研究建立了理论和实验结果之间的相关性。结果表明,AzA 抑制促炎细胞因子(COX-II、TNF-α、5-LOX、IL-17、NF-κB、IL-1β 和 IL-6)并增加抗炎细胞因子,这支持了 AzA 的抗关节炎和免疫调节潜力。