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从黎豆树根中提取的白桦脂酸和熊果酸通过与 PfEMP-1 和 PfPKG 蛋白结合来发挥其抗疟活性。

Betulinic and ursolic acids from Nauclea latifolia roots mediate their antimalarial activities through docking with PfEMP-1 and PfPKG proteins.

机构信息

Department of Biochemistry, Arthur Jarvis University, Akpabuyo, Cross River State, Nigeria.

Department of Biochemistry, University of Uyo, Uyo, Akwa Ibom State, Nigeria.

出版信息

BMC Complement Med Ther. 2024 Feb 7;24(1):79. doi: 10.1186/s12906-023-04324-x.

Abstract

BACKGROUND

Chemotherapies target the PfEMP-1 and PfPKG proteins in Plasmodium falciparum, the parasite that causes malaria, in an effort to prevent the disease's high fatality rate. This work identified the phytochemical components of Nauclea latifolia roots and docked the chemical compounds against target proteins, and examined the in vivo antiplasmodial effect of the roots on Plasmodium berghei-infected mice.

METHODS

Standard protocols were followed for the collection of the plant's roots, cleaning, and drying of the roots, extraction and fraction preparation, assessment of the in vivo antiplasmodial activity, retrieval of the PfEMP-1 and PfPKG proteins, GCMS, ADME, and docking studies, chromatographic techniques were employed to separate the residual fraction's components, and the Swis-ADME program made it possible to estimate the drug's likeness and pharmacokinetic properties. The Auto Dock Vina 4.2 tool was utilized for molecular docking analysis.

RESULTS

The residual fraction showed the best therapeutic response when compared favorably to amodiaquine (80.5%) and artesunate (85.1%). It also considerably reduced the number of parasites, with the % growth inhibition of the parasite at 42.8% (D2) and 83.4% (D5). Following purification, 25 compounds were isolated and characterized with GCMS. Based on their low molecular weights, non-permeation of the blood-brain barrier, non-inhibition of metabolizing enzymes, and non-violation of Lipinski's criteria, betulinic and ursolic acids were superior to chloroquine as the best phytochemicals. Hence, they are lead compounds.

CONCLUSION

In addition to identifying the bioactive compounds, ADME, and docking data of the lead compounds as candidates for rational drug design processes as observed against Plasmodium falciparum target proteins (PfEMP-1 and PfPKG), which are implicated in the pathogenesis of malaria, the study has validated that the residual fraction of N. latifolia roots has the best antiplasmodial therapeutic index.

摘要

背景

针对引起疟疾的寄生虫疟原虫中的 PfEMP-1 和 PfPKG 蛋白,化疗药物试图以此来预防这种疾病的高死亡率。这项工作鉴定了乌檀根的植物化学成分,并将这些化合物对接入靶蛋白,研究了乌檀根对感染伯氏疟原虫的小鼠的体内抗疟作用。

方法

按照标准程序采集植物的根,清洗并干燥根,提取和分离准备,评估体内抗疟活性,提取 PfEMP-1 和 PfPKG 蛋白,进行 GCMS、ADME 和对接研究,采用色谱技术分离残余部分的成分,利用 Swis-ADME 程序估算药物的相似性和药代动力学特性。采用 Auto Dock Vina 4.2 工具进行分子对接分析。

结果

与阿莫地喹(80.5%)和青蒿琥酯(85.1%)相比,残余部分显示出最好的治疗反应。它还显著减少了寄生虫的数量,寄生虫的增长率抑制为 42.8%(D2)和 83.4%(D5)。经纯化后,分离并鉴定了 25 种化合物,采用 GCMS。根据它们的低分子量、不穿透血脑屏障、不抑制代谢酶以及不违反 Lipinski 标准,白桦脂酸和熊果酸比氯喹更优越,是最佳的植物化学成分。因此,它们是先导化合物。

结论

除了鉴定候选药物合理设计过程中的生物活性化合物、ADME 和对接数据外,还观察到针对 PfEMP-1 和 PfPKG 等疟原虫靶蛋白的先导化合物(参与疟疾发病机制),研究证实乌檀根的残余部分具有最佳的抗疟治疗指数。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b0d/10848498/a1f91b914413/12906_2023_4324_Fig1_HTML.jpg

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