Department of Chemical Sciences, Biochemistry and Nutrition Unit, Fountain University, Osogbo, Osun State, Nigeria.
Central Research Lab, 132B, University Road, Tanke, Ilorin, Nigeria.
Acta Parasitol. 2023 Sep;68(3):659-675. doi: 10.1007/s11686-023-00698-7. Epub 2023 Jul 21.
The search for new antimalarial drugs remains elusive prompting research into antimalarial combinations from medicinal plants due to their cheapness, efficacy and availability. Azadirachta indica (AI), Morinda lucida (ML) and Mangifera indica (MI) have all been reported as potent antimalarial plants.
This study evaluated the efficacy of an antimalarial combination therapeutics prepared from leaves of AI, ML and MI using in vitro, in vivo and molecular methods.
Refined extracts of the plants combination was made by partitioning the aqueous extract of plants combinations (AI + MI, AI + ML, MI + ML, AI + MI + ML) using methanol and ethyl acetate consecutively. The resulting ethyl acetate partitioned fraction was evaluated for its antimalarial activity. Molecular docking and molecular dynamics simulation were employed to determine the possible mechanism of action of the constituent of the most active combination against four important P. falciparum proteins.
The result revealed that the refined extract from combinations AI + ML and MI + ML at 16 mg/kg bodyweight have the highest chemo-suppressive effect of 90.7% and 91.0% respectively compared to chloroquine's 100% at 10 mg/kg. Also, refined extract from MI + ML combination improved PCV levels significantly (p < 0.05) compared to controls. Molecular docking revealed oleanolic acid and ursolic acid as multiple inhibitors of plasmepsin II, hiso-aspartic protease, falcipain-2 and P. falciparum Eonyl acyl-carrier protein reductase with relative stability during 100 ns of simulation.
The study unveiled the potentials of ML and MI as good candidates for antimalarial combination therapy and further established their use together as revealed in folklore medicine.
寻找新的抗疟药物仍然难以捉摸,因此人们研究了来自药用植物的抗疟组合药物,因为它们便宜、有效且易于获得。印楝(AI)、辣木(ML)和芒果(MI)均已被报道为有效的抗疟植物。
本研究采用体外、体内和分子方法评估了由 AI、ML 和 MI 叶制备的抗疟组合疗法的疗效。
采用甲醇和乙酸乙酯依次对植物组合水提物(AI+MI、AI+ML、MI+ML、AI+MI+ML)进行萃取分离,得到精制提取物。对所得乙酸乙酯萃取部位进行抗疟活性评价。采用分子对接和分子动力学模拟方法,确定活性最强的组合成分对 4 种重要 Pf 蛋白的可能作用机制。
结果表明,与 10mg/kg 氯喹的 100%相比,16mg/kg 体重的 AI+ML 和 MI+ML 组合精制提取物的化学抑制作用最高,分别为 90.7%和 91.0%。此外,与对照组相比,MI+ML 组合的精制提取物可显著提高 PCV 水平(p<0.05)。分子对接表明,齐墩果酸和熊果酸是质体朊酶 II、组氨酸天冬氨酸蛋白酶、裂殖体蛋白酶 2 和 Pf 烯酰基载体蛋白还原酶的多重抑制剂,在 100ns 的模拟过程中相对稳定。
本研究揭示了 ML 和 MI 作为抗疟联合治疗的良好候选药物的潜力,并进一步证实了民间医学中联合使用 ML 和 MI 的用途。