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Therapeutic effect of oral quercetin in hamsters infected with . | LitMetric

Therapeutic effect of oral quercetin in hamsters infected with .

Front Cell Infect Microbiol

Laboratório de Imunofarmacologia Parasitária, Disciplina de Parasitologia/Faculdade de Ciências Médicas, Universidade do Estado do Rio de Janeiro, Rio de Janeiro, Brazil.

Published: January 2023

AI Article Synopsis

Article Abstract

Leishmaniasis is a parasitic disease caused by several species of intracellular protozoa of the genus that present manifestations ranging from cutaneous ulcers to the fatal visceral form is an important species associated with American tegumentary leishmaniasis and the main agent in Brazil, with variable sensitivity to available drugs. The search for new therapeutic alternatives to treat leishmaniasis is an urgent need, especially for endemic countries. Not only is quercetin well known for its antioxidant activity in radical scavenging but also several other biological effects are described, including anti-inflammatory, antimicrobial, and pro-oxidant activities. This study aimed to investigate the flavonoid quercetin's therapeutic potential in infection. Quercetin showed antiamastigote (IC of 21 ± 2.5 µM) and antipromastigote (25 ± 0.7 µM) activities and a selectivity index of 22. The treatment of uninfected or -infected macrophages with quercetin increased reactive oxygen species (ROS)/H0 generation without altering Nitric Oxide (NO) production. Oral treatment with quercetin of infected hamsters, starting at 1 week of infection for 8 weeks, reduced the lesion thickness (p > 0.01) and parasite load (p > 0.001). The results of this study suggest that the antiamastigote activity of the flavonoid quercetin is associated, at least in part, with the modulation of ROS production by macrophages. The efficacy of oral quercetin treatment in hamsters infected with was presented for the first time and shows its promising therapeutic potential.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9880276PMC
http://dx.doi.org/10.3389/fcimb.2022.1059168DOI Listing

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