Loading…

Biosynthesized silver nanoparticles regulate the iron status in the spleen of Plasmodium chabaudi–infected mice

Malaria is a dangerous disease affecting millions around the globe. Biosynthesized nanoparticles are used against a variety of diseases including malaria worldwide. Here, silver nanoparticles (AgNPs) synthesized from the leaf extracts of Indigofera oblongifolia have been used in the treatment of mic...

Full description

Saved in:
Bibliographic Details
Published in:Environmental science and pollution research international 2020-11, Vol.27 (32), p.40054-40060
Main Authors: Murshed, Mutee, Dkhil, Mohamed A., Al-Shaebi, Esam M., Qasem, Mahmood A. A., Mares, Mohammed M., Aljawdah, Hossam M. A., Alojayri, Ghada, Abdel-Gaber, Rewaida, Al-Quraishy, Saleh
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:Malaria is a dangerous disease affecting millions around the globe. Biosynthesized nanoparticles are used against a variety of diseases including malaria worldwide. Here, silver nanoparticles (AgNPs) synthesized from the leaf extracts of Indigofera oblongifolia have been used in the treatment of mice infected with Plasmodium chabaudi to evaluate the expression of iron regulatory genes in the spleen. Infrared spectroscopy was used to identify the expected classes of compounds in the extract. AgNPs were able to decrease the parasitemia nearly similar to the used reference drug, chloroquine. In addition, AgNPs significantly decreased the spleen index after infection. Moreover, the iron distribution was increased after the treatment. Finally, AgNPs could regulate the mice spleen iron regulatory genes, Lipocalin 2 ( Lcn2 ), transferrin receptor 1 ( TFR1 ) and hepcidin antimicrobial peptide ( Hamp ). Taken together, our findings indicate that AgNPs have antimalarial activity and can control the state of iron in spleen. We need further investigations to determine mechanisms of action of the AgNPs.
ISSN:0944-1344
1614-7499
DOI:10.1007/s11356-020-10027-4