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提取物各组分的抗关节炎和抗炎潜力:一种计算机模拟、体外和体内研究方法。

Anti-Arthritic and Anti-Inflammatory Potential of Extract Fractions: An In Silico, In Vitro and In Vivo Approach.

作者信息

Khalid Mohammad, Alqarni Mohammed H, Shoaib Ambreen, Arif Muhammad, Foudah Ahmed I, Afzal Obaid, Ali Abuzer, Ali Amena, Alqahtani Saad S, Altamimi Abdulmalik S A

机构信息

Department of Pharmacognosy, College of Pharmacy, Prince Sattam Bin Abdulaziz University, P.O. Box 173, Al-Kharj 11942, Saudi Arabia.

Department of Clinical Pharmacy, College of Pharmacy, Jazan University, Jazan 45142, Saudi Arabia.

出版信息

Plants (Basel). 2021 Apr 21;10(5):825. doi: 10.3390/plants10050825.

Abstract

The fruits of have traditionally been used for the management of rheumatism in the northeast region of India. The present study explores the probable anti-arthritis and anti-inflammatory potential of fruit extract's ethanolic fraction (EtoH-F). To support this study, we first approached the parameters in silico by means of the active constituents of the plant (beta amyrin, beta sitosterol, oleonolic acid and co-crystallised ligands, i.e., SPD-304) via molecular docking on COX-1, COX-2 and TNF-α. Thereafter, the absorption, distribution, metabolism, excretion and toxicity properties were also determined, and finally experimental activity was performed in vitro and in vivo. The in vitro activities of the plant extract fractions were evaluated by means of parameters like 1,1-Diphenyl-2- picrylhydrazyl (DPPH), free radical-reducing potential, albumin denaturation, and protease inhibitory activity. The in vivo activity was evaluated using parameters like COX, TNF-α and IL-6 inhibition assay and arthritis score in Freund Adjuvant (CFA) models at a dose of 400 mg/kg b.w. per day of different fractions (hexane, chloroform, alcoholic). The molecular docking assay was performed on COX-1, COX-2 and TNF-α. The results of in vitro studies showed concentration-dependent reduction in albumin denaturation, protease inhibitors and scavenging activity at 500 µg/mL. Administration of the alcoholic fraction at the abovementioned dose resulted in a significant reduction ( < 0.01) in arthritis score, paw diameters, TNF-α, IL-6 as compared to diseased animals. The docking results showed that residues show a critical binding affinity with TNF-α and act as the TNF-α antagonist. The alcoholic fraction of extract possesses beneficial effects on rheumatoid arthritis as well as anti-inflammatory potential, and can further can be used as a possible agent for novel target-based therapies for the management of arthritis.

摘要

在印度东北地区,[植物名称]的果实传统上被用于治疗风湿病。本研究探讨了[植物名称]果实提取物乙醇馏分(EtoH-F)可能的抗关节炎和抗炎潜力。为支持本研究,我们首先通过分子对接COX-1、COX-2和TNF-α,借助植物的活性成分(β-香树脂醇、β-谷甾醇、齐墩果酸和共结晶配体,即SPD-304)在计算机上研究相关参数。此后,还测定了其吸收、分布、代谢、排泄和毒性特性,最后进行了体外和体内实验活性研究。通过1,1-二苯基-2-苦基肼(DPPH)、自由基还原潜力、白蛋白变性和蛋白酶抑制活性等参数评估了植物提取物馏分的体外活性。在弗氏佐剂(CFA)模型中,以每天400 mg/kg体重的剂量使用不同馏分(己烷、氯仿、乙醇),通过COX、TNF-α和IL-6抑制试验以及关节炎评分等参数评估体内活性。对COX-1、COX-2和TNF-α进行了分子对接试验。体外研究结果表明,在500 µg/mL时,白蛋白变性、蛋白酶抑制剂和清除活性呈浓度依赖性降低。与患病动物相比,以上述剂量给予[植物名称]乙醇馏分可使关节炎评分、爪直径、TNF-α、IL-6显著降低(P<0.01)。对接结果表明,[植物名称]的某些残基与TNF-α显示出关键的结合亲和力,并可作为TNF-α拮抗剂。[植物名称]提取物的乙醇馏分对类风湿性关节炎具有有益作用以及抗炎潜力,可进一步用作基于新靶点治疗关节炎的可能药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9149/8143105/5d9f7ebd21ab/plants-10-00825-g001.jpg

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