Olaoye Ige Francis, Oso Babatunde Joseph, Aberuagba Adepeju
Department of Biochemistry, McPherson University, Seriki Sotayo, Ogun State, Nigeria.
Department of Biochemistry, University of Ilorin, Ilorin, Kwara State, Nigeria.
Avicenna J Med Biotechnol. 2021 Oct-Dec;13(4):207-216.
A large body of literature suggests that the extracts of . and (. ) play protective roles against various inflammatory disorders. However, the possible mechanism of action with reference to the interactions of their respective phytochemical compositions with pro-inflammatory mediators as the indication of their therapeutic effects is less clear. Therefore, the immunomodulatory properties of . and . were investigated in this study.
The lipoxygenase inhibitory potentials of methanolic extracts of the selected plants were assessed through colorimetric analysis. The pharmacokinetics of some identified compounds in the botanicals were investigated the Swiss ADME server while the molecular interactions of the compounds with lipoxygenase, IL-1, IL-6, TNF-α, IL-8, and CCL-2 were performed through molecular docking.
The assessment of the lipoxygenase inhibition revealed the extracts could possess anti-inflammatory agents. The pharmacokinetic results of some selected compounds identified in the botanicals showed moderate toxic effects compared to indomethacin. The molecular docking study substantiated the report of the analysis as indicated in the binding score of all the selected compounds compared to indomethacin.
The phytochemical components of the extracts of and could be effective as anti-inflammatory agents that could be explored in preventing disorders associated with excessive activities of pro-inflammatory mediators.
大量文献表明,[植物名称1]和[植物名称2]([植物拉丁学名1]和[植物拉丁学名2])的提取物对各种炎症性疾病具有保护作用。然而,关于它们各自的植物化学成分与促炎介质相互作用作为其治疗效果指标的可能作用机制尚不清楚。因此,本研究对[植物名称1]和[植物名称2]的免疫调节特性进行了研究。
通过比色分析评估所选植物甲醇提取物的12-脂氧合酶抑制潜力。利用瑞士ADME服务器研究了植物中一些已鉴定化合物的药代动力学,同时通过分子对接研究了这些化合物与脂氧合酶、白细胞介素-1、白细胞介素-6、肿瘤坏死因子-α、白细胞介素-8和趋化因子配体-2的分子相互作用。
脂氧合酶抑制评估表明提取物可能含有抗炎剂。植物中一些选定化合物的药代动力学结果显示,与吲哚美辛相比,其毒性作用中等。分子对接研究证实了比色分析的结果,所有选定化合物与吲哚美辛相比的结合分数表明了这一点。
[植物名称1]和[植物名称2]提取物中的植物化学成分可能作为抗炎剂有效,可用于预防与促炎介质过度活动相关的疾病。