Biogenically synthesized green silver nanoparticles exhibit antimalarial activity

被引:2
作者
Tiwari, Savitri [1 ]
Kumar, Reetesh [2 ]
Devi, Sonia [3 ,4 ]
Sharma, Prakriti [3 ]
Chaudhary, Neil Roy [3 ]
Negi, Sushmita [3 ,4 ]
Tandel, Nikunj [5 ,8 ]
Marepally, Srujan [6 ]
Pied, Sylviane [6 ,7 ]
Tyagi, Rajeev K. [3 ,4 ]
机构
[1] Galgotias Univ, Sch Biol & Life Sci, Greater Noida 201310, India
[2] GLA Univ, Inst Appl Sci & Humanities, Fac Agr Sci, Mathura 281406, India
[3] CSIR Inst Microbial Technol IMTECH, Div Cell Biol & Immunol, Biomed Parasitol & Translat Immunol Lab, Sec 39A, Chandigarh 160036, India
[4] Acad Sci & Innovat Res AcSIR, Ghaziabad 201002, India
[5] Nirma Univ, Inst Sci, Ahmadabad, Gujarat, India
[6] Christian Med Coll Campus, Ctr Stem Cell Res, Unit inStem, Vellore 632002, Tamil Nadu, India
[7] Univ Lille, Inst Pasteur Lille, Ctr Infect & Immun Lille CIIL 9, CNRS UMR 9017 INSERM U1019, F-59019 Lille, France
[8] CSIR Ctr Cellular & Mol Biol CCMB, Malaria Res Lab, Hyderabad 500007, Telangana, India
关键词
Euphorbia cotinifolia; Nanoparticle; Plasmodium falciparum; Apoptosis; Drug resistance; Reactive oxygen species (ROS) production; Cell death; PLASMODIUM-FALCIPARUM; ANTIPLASMODIAL ACTIVITY; OXIDATIVE STRESS; CELL-DEATH; IN-VIVO; MALARIA; THIOREDOXIN; GLUTATHIONE; EXPRESSION; STRATEGIES;
D O I
10.1186/s11671-024-04098-2
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
The suboptimal efficacies of existing anti-malarial drugs attributed to the emergence of drug resistance dampen the clinical outcomes. Hence, there is a need for developing novel drug and drug targets. Recently silver nanoparticles (AgNPs) constructed with the leaf extracts of Euphorbia cotinifolia were shown to possess antimalarial activity. Therefore, the synthesized AgNPs from Euphorbia cotinifolia (EcAgNPs) were tested for their parasite clearance activity. We determined the antimalarial activity in the asexual blood stage infection of 3D7 (laboratory strain) P. falciparum. EcAgNPs demonstrated the significant inhibition of parasite growth (EC50 of 0.75 mu g/ml) in the routine in vitro culture of P. falciparum. The synthesized silver nanoparticles were seen to induce apoptosis in P. falciparum through increased reactive oxygen species (ROS) ROS production and activated programmed cell death pathways characterized by the caspase-3 and calpain activity. Also, altered transcriptional regulation of Bax/Bcl-2 ratio indicated the enhanced apoptosis. Moreover, inhibited expression of PfLPL-1 by EcAgNPs is suggestive of the dysregulated host fatty acid flux via parasite lipid storage. Overall, our findings suggest that EcAgNPs are a non-toxic and targeted antimalarial treatment, and could be a promising therapeutic approach for clearing malaria infection.
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页数:21
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