{"title":"Antimalarial activity of Toona ciliata MJ Roem aqueous methanolic leaf extract and its antioxidant and phytochemical properties","authors":"Nalini Singh , Aditi Chatterjee , Wahengbam Kabita Chanu , Pradeep Mini Vaishalli , Chingakham Brajakishor Singh , Viswanathan Arun Nagaraj","doi":"10.1016/j.jtcme.2023.05.004","DOIUrl":null,"url":null,"abstract":"<div><h3>Background and aim</h3><p>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 <em>Toona ciliata</em> MJ Roem aqueous methanolic leaf extract (<em>Tc</em>MLE).</p></div><div><h3>Experimental procedures</h3><p><em>In vitro</em> antiplasmodial studies in <em>Plasmodium falciparum</em> (<em>Pf</em>) 3D7 and <em>Pf</em>Cam3.I<sup>R539T</sup> strains were performed by [<sup>3</sup>H]-hypoxanthine uptake assays. <em>In vitro</em> cytotoxicity in HeLa and HEK293T cell lines was evaluated using MTT assays. Hemolysis assay was performed using RBCs. Phytochemical analysis by GC-MS and <em>in vitro</em> antioxidant studies by DPPH and ABTS assays were performed. <em>In vivo</em> antimalarial studies in <em>Pb</em>-infected mice were carried out using Rane's test and Peters' 4-day test.</p></div><div><h3>Results and conclusions</h3><p><em>Tc</em>MLE showed significant <em>in vitro</em> antioxidant activity and had phytochemicals reported for antimalarial activity. <em>In vitro</em> studies showed prominent antiplasmodial activity against <em>Pf</em>3D7 strain (IC<sub>50</sub> ∼22 μg/ml) and <em>Pf</em>Cam3. I<sup>R539T</sup>strain (IC<sub>50</sub> value ∼43 μg/ml). <em>In vitro</em> cytotoxicity studies, <em>in vitro</em> hemolytic assays, and <em>in vivo</em> acute toxicity studies further suggested that <em>Tc</em>MLE is nontoxic. <em>In vivo</em> 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 <em>Tc</em>MLE. These findings deliver a platform for further studies to identify the active components of <em>Tc</em>MLE and discover new antimalarials.</p></div>","PeriodicalId":3,"journal":{"name":"ACS Applied Electronic Materials","volume":null,"pages":null},"PeriodicalIF":4.3000,"publicationDate":"2023-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"2","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Applied Electronic Materials","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2225411023000597","RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ENGINEERING, ELECTRICAL & ELECTRONIC","Score":null,"Total":0}
引用次数: 2
Abstract
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.