Suppr超能文献

评估氨氯地平作为抗关节炎药物的疾病修饰潜力:老药新用。

Appraisal of disease-modifying potential of amlodipine as an anti-arthritic agent: new indication for an old drug.

机构信息

Laboratory of Cardiovascular Research and Integrative Pharmacology, College of Pharmacy, University of Sargodha, Sargodha, Pakistan.

College of Pharmacy, Jouf University, Sakaka, Al Jouf, Saudi Arabia.

出版信息

Inflammopharmacology. 2020 Aug;28(4):1121-1136. doi: 10.1007/s10787-020-00692-9. Epub 2020 Mar 5.

Abstract

Amlodipine, a second-generation calcium channel blocker, exhibits documented anti-inflammatory potential. Thereby, present investigation was accomplished with an aim to explore anti-arthritic potential of amlodipine, giving a second chance to an existing drug. For validation of anti-arthritic potential of amlodipine, some in vitro models comprised of bovine serum albumin- and egg albumin-induced protein denaturation along with membrane stabilization of red blood cell was being conducted. In vivo models comprised of formaldehyde-provoked acute arthritis and CFA-instigated chronic arthritic. Paw edema, arthritic index, body weight alterations, biochemical and hematological parameters, and ankle joint histological and radiographic investigations were appraised. Moreover, RT-PCR was conducted to evaluate the levels of several inflammatory markers. Molecular docking was being conducted targeting TNF-α, IL-1β and IL-6 to establish the correlation between experimental and theoretical results. Amlodipine provides significant protection against denaturation being provoked by heating egg albumin and BSA along with stabilizing membrane of red blood cell, thereby proving in vitro anti-arthritic effect. A significant (p < 0.001) reduction in paw swelling was being observed with amlodipine in case of formaldehyde-instigated arthritis especially at the dose of 20 mg/kg. In case of CFA-provoked arthritis, reduction in paw volume and arthritic score while preservation of body weight loss and normal hematological and biochemical parameters in comparison to arthritic control were being manifested by amlodipine at the dose of 20 mg/kg. Gene expression level of TNF-α, IL-6 and IL-1β was significantly reduced by amlodipine while an increase in expression level of IL-4 and IL-10 was evident in animals treated with piroxicam and amlodipine. Molecular docking analysis demonstrated strong binding interaction of amlodipine with TNF-α, IL-6 and IL-1β thus providing a good correlation between experimental and theoretical results. Thus, current study is suggestive that amlodipine exhibits strong anti-arthritic potential and thus can be considered as a candidate for drug repurposing as anti-arthritic agent.

摘要

氨氯地平是第二代钙通道阻滞剂,具有明确的抗炎潜力。因此,本研究旨在探索氨氯地平的抗关节炎潜力,为现有药物提供第二次机会。为了验证氨氯地平的抗关节炎潜力,进行了一些体外模型,包括牛血清白蛋白和卵白蛋白诱导的蛋白质变性以及红细胞膜稳定。体内模型包括甲醛诱导的急性关节炎和 CFA 诱导的慢性关节炎。评估了爪肿胀、关节炎指数、体重变化、生化和血液学参数以及踝关节组织学和放射照相研究。此外,还进行了 RT-PCR 以评估几种炎症标志物的水平。进行了针对 TNF-α、IL-1β 和 IL-6 的分子对接,以建立实验和理论结果之间的相关性。氨氯地平对卵白蛋白和 BSA 加热引起的变性以及稳定红细胞膜提供了显著的保护,从而证明了其体外抗关节炎作用。在甲醛诱导的关节炎中,氨氯地平显著(p<0.001)减少爪肿胀,特别是在 20mg/kg 剂量下。在 CFA 诱导的关节炎中,与关节炎对照组相比,氨氯地平在 20mg/kg 剂量下可减少爪体积和关节炎评分,同时保持体重减轻和正常血液生化参数。氨氯地平可显著降低 TNF-α、IL-6 和 IL-1β 的基因表达水平,而用吡罗昔康和氨氯地平治疗的动物的 IL-4 和 IL-10 的表达水平增加。分子对接分析表明,氨氯地平与 TNF-α、IL-6 和 IL-1β 具有很强的结合相互作用,从而为实验和理论结果之间提供了良好的相关性。因此,本研究表明氨氯地平具有很强的抗关节炎潜力,因此可以考虑将其作为抗关节炎药物重新利用的候选药物。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验