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新型酰腙衍生物通过抑制 NF-κB 信号通路和 HSP70/HSP90 蛋白缓解关节炎模型。

Inhibition of NF-κB signaling and HSP70/HSP90 proteins by newly synthesized hydrazide derivatives in arthritis model.

机构信息

Pharmacological Sciences Research Lab, Department of Pharmacy, Faculty of Biological Sciences, Quaid-i-Azam University, Islamabad, Pakistan.

Department of Chemistry, The University of Azad Jammu and Kashmir, Muzaffarabad, 13100, Pakistan.

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 2021 Jul;394(7):1497-1519. doi: 10.1007/s00210-021-02075-5. Epub 2021 Mar 13.

Abstract

In the current study, the N-benzylidene-4-((2-hydroxynaphthalene-1-yl) diazenyl) hydrazides (NCHDH and NTHDH) were evaluated against the Carrageenan- and CFA-induced models. During the preliminary investigation, the NCHDH and NTHDH treatment showed marked anti-inflammatory and analgesic activity against the Carrageenan-induced acute model. Once the anti-inflammatory activity was established against acute Carrageenan model, the NCHDH and NTHDH were evaluated against the chronic CFA-induced arthritis model. The NCHDH and NTHDH treatment markedly attenuated the inflammatory and analgesic parameters compared to CFA-treated group. Furthermore, the increase in the oxidative stress and attenuation of antioxidant enzymes has been reported following CFA administration. However, NCHDH and NTHDH treatment significantly induced the antioxidants and attenuated the oxidative stress markers. The CFA administration showed marked tailing of DNA; however, the NCHDH- and NTHDH-treated group preserved DNA integrity. Furthermore, the histological studies showed marked alteration in the CFA-treated group; however, the NCHDH and NTHDH treatment markedly improved the histological features. The Western blot, immunohistology, and ELISA assay revealed marked increase in the Nuclear factor kappa-light-chain-enhancer of activated B cells (NF-κB), Jun N-terminal Kinase (JNK), TNF-α, and COX-2 levels; however, the NCHDH and NTHDH attenuated their expressions significantly. Similarly, the NCHDH and NTHDH significantly induced the mRNA expression levels of heat shock proteins. The computational analysis showed significant binding interaction with various protein targets via multiple hydrogens, and hydrophobic bonds. The in vivo pharmacokinetic study was also performed to assess the various pharmacokinetic parameters. In conclusion, the NCHDH and NTHDH treatment showed significant anti-arthritic activity against Carrageenan and CFA models.

摘要

在当前的研究中,N-苄叉-4-((2-羟基萘-1-基)偶氮基)腙(NCHDH 和 NTHDH)被评估用于角叉菜胶和 CFA 诱导的模型。在初步研究中,NCHDH 和 NTHDH 治疗对角叉菜胶诱导的急性模型表现出明显的抗炎和镇痛活性。一旦对急性角叉菜胶模型建立了抗炎活性,就评估了 NCHDH 和 NTHDH 对慢性 CFA 诱导的关节炎模型的作用。与 CFA 处理组相比,NCHDH 和 NTHDH 治疗明显减轻了炎症和镇痛参数。此外,据报道,CFA 给药后氧化应激增加,抗氧化酶减少。然而,NCHDH 和 NTHDH 治疗显著诱导抗氧化剂并减弱氧化应激标志物。CFA 给药导致 DNA 明显拖尾;然而,NCHDH 和 NTHDH 处理组保持 DNA 完整性。此外,组织学研究显示 CFA 处理组有明显改变;然而,NCHDH 和 NTHDH 治疗显著改善了组织学特征。Western blot、免疫组织化学和 ELISA 检测显示核因子 kappa-轻链增强子的激活 B 细胞(NF-κB)、Jun N-末端激酶(JNK)、TNF-α和 COX-2 水平显著增加;然而,NCHDH 和 NTHDH 显著减弱了它们的表达。同样,NCHDH 和 NTHDH 显著诱导热休克蛋白的 mRNA 表达水平。计算分析显示通过多个氢键和疏水键与各种蛋白质靶标具有显著的结合相互作用。还进行了体内药代动力学研究以评估各种药代动力学参数。总之,NCHDH 和 NTHDH 治疗对角叉菜胶和 CFA 模型表现出显著的抗关节炎活性。

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