A Review on Therapeutic Activities of Coriandrum sativum L for Rheumatoid Arthritis Remedy

Mikidadi S. Gurisha, Papula V. Kanaka Rao, Laxmikanth Cherupally, Alex J. Mbise
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Abstract

Rheumatoid Arthritis (RA) is an immune-mediated inflammatory condition. It occurs when the immune system attacks the tissue surrounding joints due to the release of specific chemicals and enzymes that start consuming away the cartilage and bones. The ant-arthritis of Coriandrum sativum (CS) has not been summarized before, so this review aims to assess further and explore its efficacy in RA disorders. The online literature search was performed using databases such as ScienceDirect, PubMed, Google Scholar, Wiley Online, Library, Springer, and Taylor& Francis for review. Articles published from January 2010 to January 2024 were composed. Additionally, the molecular docking of the eight selected CS phytochemicals was carried out against the AR protein target (PDB ID: 2AXJ) to support the review. Different parameters such as docking score, oral bioavailability, drug-likeness, absorption, distribution, metabolism, excretion, and toxicity (ADMET) were examined. Docking scores depicted that, anethole, beta-pinene, camphor, and geraniol phytochemicals demonstrated a commendable potential as inhibitors of 2AXJ molecule. The score hierarchy is camphor (-6.9 kcal/mol), beta-pinene (-5.9 kcal/mol), geraniol (-5.3 kcal/mol), and anethole (-5.2 kcal/mol).  The four phytochemicals also appear to have good drug-likeness properties and oral bioavailability. Therefore the in vitro and in vivo studies have demonstrated that CS has strong potential as anti-arthritics and anti-inflammatory. However, clinical trials for both fresh and extracted CS are also necessary to validate the findings.
类风湿性关节炎疗法中的芫荽治疗活性综述
类风湿性关节炎(RA)是一种免疫介导的炎症。当免疫系统攻击关节周围的组织时,就会释放出特定的化学物质和酶,开始吞噬软骨和骨骼。此前尚未对芫荽(Coriandrum sativum,CS)的抗关节炎作用进行总结,因此本综述旨在进一步评估和探讨其对 RA 疾病的疗效。在线文献检索使用的数据库包括 ScienceDirect、PubMed、Google Scholar、Wiley Online、Library、Springer 和 Taylor& Francis。文章发表于 2010 年 1 月至 2024 年 1 月。此外,还对所选的八种 CS 植物化学物质与 AR 蛋白靶标(PDB ID:2AXJ)进行了分子对接,以支持综述。研究考察了对接得分、口服生物利用度、药物相似性、吸收、分布、代谢、排泄和毒性(ADMET)等不同参数。对接得分表明,茴香烯、β-蒎烯、樟脑和香叶醇等植物化学物质具有作为 2AXJ 分子抑制剂的巨大潜力。分级为樟脑(-6.9 kcal/mol)、β-蒎烯(-5.9 kcal/mol)、香叶醇(-5.3 kcal/mol)和茴香烯(-5.2 kcal/mol)。 这四种植物化学物质似乎还具有良好的药物相似性和口服生物利用度。因此,体外和体内研究表明,CS 具有很强的抗关节炎和消炎潜力。不过,还需要对新鲜和提取的 CS 进行临床试验,以验证研究结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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