香椿叶甲醇提取物的抗疟活性及其抗氧化和植物化学性质

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
Nalini Singh , Aditi Chatterjee , Wahengbam Kabita Chanu , Pradeep Mini Vaishalli , Chingakham Brajakishor Singh , Viswanathan Arun Nagaraj
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引用次数: 2

摘要

背景和目的疟疾是造成大量发病率和死亡率的全球性健康问题。筛选各种传统上重要的药用植物是发现新的抗疟药物的关键来源。研究了香椿叶甲醇水提物(TcMLE)的抗疟活性和抗氧化活性,并进行了详细的植物化学分析。实验方法:恶性疟原虫(Pf) 3D7和PfCam3的体外抗疟原虫研究。采用[3H]-次黄嘌呤摄取法测定IR539T菌株。采用MTT法评价HeLa和HEK293T细胞株的体外细胞毒性。采用红细胞进行溶血试验。采用气相色谱-质谱法进行植物化学分析,DPPH和ABTS法进行体外抗氧化研究。采用Rane试验和Peters 4天试验对pb感染小鼠进行体内抗疟研究。结果与结论stcmle具有显著的体外抗氧化活性,并有植物化学物质具有抗疟活性。体外研究显示对Pf3D7菌株(IC50 ~ 22 μg/ml)和PfCam3具有显著的抗疟原虫活性。ir539strain (IC50值~ 43 μg/ml)。体外细胞毒性研究、体外溶血试验和体内急性毒性研究进一步表明,TcMLE是无毒的。使用Rane试验的体内抗疟疾研究表明,在1200mg /kg剂量下,寄生虫血症显著降低~ 70%,并将小鼠的死亡延迟~ 10-14天。彼得斯为期4天的测试也显示出类似的模式。本研究证实了TcMLE的抗疟潜力。这些发现为进一步研究确定TcMLE的有效成分和发现新的抗疟药物提供了一个平台。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Antimalarial activity of Toona ciliata MJ Roem aqueous methanolic leaf extract and its antioxidant and phytochemical properties

Antimalarial activity of Toona ciliata MJ Roem aqueous methanolic leaf extract and its antioxidant and phytochemical properties

Background and aim

Malaria is a global health issue causing substantial morbidity and mortality. Screening of various traditionally important medicinal plants is a key source for the discovery of new antimalarials. We evaluated the antimalarial and antioxidant activities, and performed detailed phytochemical analyses of Toona ciliata MJ Roem aqueous methanolic leaf extract (TcMLE).

Experimental procedures

In vitro antiplasmodial studies in Plasmodium falciparum (Pf) 3D7 and PfCam3.IR539T strains were performed by [3H]-hypoxanthine uptake assays. In vitro cytotoxicity in HeLa and HEK293T cell lines was evaluated using MTT assays. Hemolysis assay was performed using RBCs. Phytochemical analysis by GC-MS and in vitro antioxidant studies by DPPH and ABTS assays were performed. In vivo antimalarial studies in Pb-infected mice were carried out using Rane's test and Peters' 4-day test.

Results and conclusions

TcMLE showed significant in vitro antioxidant activity and had phytochemicals reported for antimalarial activity. In vitro studies showed prominent antiplasmodial activity against Pf3D7 strain (IC50 ∼22 μg/ml) and PfCam3. IR539Tstrain (IC50 value ∼43 μg/ml). In vitro cytotoxicity studies, in vitro hemolytic assays, and in vivo acute toxicity studies further suggested that TcMLE is nontoxic. In vivo antimalarial studies using Rane's test showed a significant decrease in parasitemia by ∼70% at 1200 mg/kg doses and delayed the mortality of mice by ∼10–14 days. Peters' 4-day test also showed a similar pattern. The present study demonstrated the antimalarial potential of TcMLE. These findings deliver a platform for further studies to identify the active components of TcMLE and discover new antimalarials.

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CiteScore
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