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赖诺普利通过靶向炎症和氧化还原失调减轻弗氏佐剂诱导的大鼠关节炎:JAK-2/STAT-3/RANKL 轴、MMPs 和 VEGF 的作用。

Targeting inflammation and redox perturbations by lisinopril mitigates Freund's adjuvant-induced arthritis in rats: role of JAK-2/STAT-3/RANKL axis, MMPs, and VEGF.

机构信息

Department of Pharmacology and Toxicology, College of Pharmacy, Taif University, P.O. Box 11099, Taif, 21944, Saudi Arabia.

Department of Pharmacy, Kut University College, Al Kut, Wasit, 52001, Iraq.

出版信息

Inflammopharmacology. 2022 Oct;30(5):1909-1926. doi: 10.1007/s10787-022-00998-w. Epub 2022 Jun 28.

Abstract

BACKGROUND

Cardiovascular disorders are major complications of rheumatoid arthritis (RA). Hence, finding effective agents that can target RA progression and its cardiovascular consequences is demanding. The present work aimed to explore the potential of lisinopril, an angiotensin-converting enzyme inhibitor, to mitigate adjuvant's-induced arthritis with emphasis on the pro-inflammatory signals, articular degradation cues, and angiogenesis alongside JAK-2/STAT-3 and Nrf2/HO-1 pathways.

METHODS

Lisinopril (10 mg/kg/day) was administered by oral gavage for 3 weeks and the target signals were examined by biochemical assays, ELISA, histopathology, immunoblotting, and immunohistochemistry.

RESULTS

Lisinopril attenuated the progression of arthritis as proven by lowering paw edema, arthritic index, and gait scores alongside diminishing the immune-cell infiltration/aberrant histopathology in the dorsal pouch lining. These favorable actions were associated with curtailing the production of inflammatory cytokines (TNF-α, IL-6, IL-1β, and IL-17) and the pro-inflammatory angiotensin II alongside upregulating the anti-inflammatory angiotensin-(1-7) in the hind paw of arthritic rats. At the molecular level, lisinopril inhibited the upstream JAK-2/STAT-3 pathway by downregulating the protein expression of p-JAK-2/total JAK-2 and p-STAT-3/total STAT-3 ratio and the nuclear levels of NF-κBp65. Meanwhile, lisinopril curbed the downstream cartilage degradation signals matrix metalloproteinases (MMP-3 and MMP-9) and the bone erosion cue RANKL. Equally important, the protein expression of the angiogenesis signal VEGF was downregulated in the hind paw/dorsal lining. With respect to oxidative stress, lisinopril suppressed the paw lipid peroxides and boosted GSH and Nrf-2/HO-1 pathway.

CONCLUSION

Lisinopril attenuated adjuvant-induced arthritis via inhibition of inflammation, articular degradation cues, and angiogenesis.

摘要

背景

心血管疾病是类风湿关节炎(RA)的主要并发症。因此,寻找能够靶向 RA 进展及其心血管后果的有效药物是非常有必要的。本研究旨在探讨血管紧张素转换酶抑制剂赖诺普利(Lisinopril)减轻佐剂诱导性关节炎的潜力,重点关注促炎信号、关节降解线索和血管生成以及 JAK-2/STAT-3 和 Nrf2/HO-1 通路。

方法

赖诺普利(10mg/kg/天)通过口服灌胃给药 3 周,通过生化测定、ELISA、组织病理学、免疫印迹和免疫组化检测靶信号。

结果

赖诺普利通过降低爪肿胀、关节炎指数和步态评分以及减少背部囊衬里免疫细胞浸润/异常组织病理学,减轻了关节炎的进展。这些有利作用与减少炎症细胞因子(TNF-α、IL-6、IL-1β 和 IL-17)和促炎血管紧张素 II 的产生以及在关节炎大鼠后爪中上调抗炎血管紧张素-(1-7)有关。在分子水平上,赖诺普利通过下调 p-JAK-2/总 JAK-2 和 p-STAT-3/总 STAT-3 比值以及核 NF-κBp65 蛋白表达来抑制上游 JAK-2/STAT-3 通路。同时,赖诺普利抑制了下游软骨降解信号基质金属蛋白酶(MMP-3 和 MMP-9)和骨侵蚀信号 RANKL。同样重要的是,后爪/背部衬里的血管生成信号 VEGF 的蛋白表达也下调。关于氧化应激,赖诺普利抑制爪脂质过氧化物并增加 GSH 和 Nrf-2/HO-1 通路。

结论

赖诺普利通过抑制炎症、关节降解线索和血管生成来减轻佐剂诱导性关节炎。

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