Inhibitory Effect of Active Substances of Lollyfish (Holothuria atra) Against the Development of Plasmodium falciparum Based on In Silico Study

Felly Moelyadi, P. Utami, Irmawati M. Dikman
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引用次数: 3

Abstract

The high level of artemisinin resistance as the antimalarial drug makes the active substances found of lollyfish (Holothuria atra) become a very useful discovery as a new antimalarial drug. The purpose of this research is to find out the inhibitory effect of the active substances of lollyfish against the development of Plasmodium falciparum with in silico method. This is a one-shot experimental study research. Based on the test of potentially active substances of lollyfish through PubChem (https://pubchem.ncbi.nlm.nih.gov/), there are pyrogallol and catechin that have potential as the antimalarial drug. Pyrogallol, chlorogenic acid, catechin dan ascorbic acid have indirect inhibition to P. falciparum Orotidine 5-Monophosphate Decarboxylase (PfOMPDC) through carbon dioxide (CO 2 ) and it is visualized by STITCH DB Version 5.0 (http://stitch.embl.de/). The binding affinity score of catechin, obtained from molecular docking, is higher than other substances and artemisinin. The Physicochemical and pharmacokinetic activity of the substance was predicted through SWISS ADME (http://www.swissadme.ch/index.php), while the toxicity was predicted through Pro-Tox (http://tox.charite.de/protox_II/). Catechin is a substance in lollyfish that is the safest because its lowest toxicity and very effective to be used as the antimalarial drug because of its high lethal dose 50 (LD50). Therefore, active substances in lollyfish have inhibitory effects against the development of P. falciparum based on in silico study.
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糖鱼(Holothuria atra)活性物质对恶性疟原虫生长抑制作用的硅基研究
青蒿素作为抗疟药物的高耐药性使得糖鱼(Holothuria atra)的活性物质成为一种非常有用的抗疟新药的发现。本研究的目的是用硅片法研究冰糖鱼的活性物质对恶性疟原虫的抑制作用。这是一项一次性实验研究。通过PubChem (https://pubchem.ncbi.nlm.nih.gov/)对棒棒鱼的潜在活性物质进行了测试,发现邻苯三酚和儿茶素有可能成为抗疟疾药物。邻苯三酚、绿原酸、儿茶素和抗坏血酸通过二氧化碳间接抑制恶性疟原虫Orotidine 5-Monophosphate Decarboxylase (PfOMPDC),并通过STITCH DB Version 5.0 (http://stitch.embl.de/)可视化。通过分子对接得到的儿茶素的结合亲和力评分高于其他物质和青蒿素。通过SWISS ADME (http://www.swissadme.ch/index.php)预测该物质的物理化学和药代动力学活性,通过Pro-Tox (http://tox.charite.de/protox_II/)预测其毒性。儿茶素是糖鱼中最安全的一种物质,因为它的毒性最低,而儿茶素作为抗疟药物是非常有效的,因为它的致死剂量(LD50)很高。因此,通过对冰糖鱼体内活性物质的体外实验,可以看出冰糖鱼体内的活性物质对恶性疟原虫具有抑制作用。
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