Interference with hemozoin formation represents an important mechanism of schistosomicidal action of antimalarial quinoline methanols.

BACKGROUND: The parasitic trematode Schistosoma mansoni is one of the major causative agents of human schistosomiasis, which afflicts 200 million people worldwide. Praziquantel remains the main drug used for schistosomiasis treatment, and reliance on the single therapy has been prompting the search...

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Main Authors: Juliana B R Corrêa Soares, Diego Menezes, Marcos A Vannier-Santos, Antonio Ferreira-Pereira, Giulliana T Almeida, Thiago M Venancio, Sergio Verjovski-Almeida, Vincent K Zishiri, David Kuter, Roger Hunter, Timothy J Egan, Marcus F Oliveira
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2009-01-01
Series:PLoS Neglected Tropical Diseases
Online Access:http://europepmc.org/articles/PMC2703804?pdf=render
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author Juliana B R Corrêa Soares
Diego Menezes
Marcos A Vannier-Santos
Antonio Ferreira-Pereira
Giulliana T Almeida
Thiago M Venancio
Sergio Verjovski-Almeida
Vincent K Zishiri
David Kuter
Roger Hunter
Timothy J Egan
Marcus F Oliveira
author_facet Juliana B R Corrêa Soares
Diego Menezes
Marcos A Vannier-Santos
Antonio Ferreira-Pereira
Giulliana T Almeida
Thiago M Venancio
Sergio Verjovski-Almeida
Vincent K Zishiri
David Kuter
Roger Hunter
Timothy J Egan
Marcus F Oliveira
author_sort Juliana B R Corrêa Soares
collection DOAJ
description BACKGROUND: The parasitic trematode Schistosoma mansoni is one of the major causative agents of human schistosomiasis, which afflicts 200 million people worldwide. Praziquantel remains the main drug used for schistosomiasis treatment, and reliance on the single therapy has been prompting the search for new therapeutic compounds against this disease. Our group has demonstrated that heme crystallization into hemozoin (Hz) within the S. mansoni gut is a major heme detoxification route with lipid droplets involved in this process and acting as a potential chemotherapeutical target. In the present work, we investigated the effects of three antimalarial compounds, quinine (QN), quinidine (QND) and quinacrine (QCR) in a murine schistosomiasis model by using a combination of biochemical, cell biology and molecular biology approaches. METHODOLOGY/PRINCIPAL FINDINGS: Treatment of S. mansoni-infected female Swiss mice with daily intraperitoneal injections of QN, and QND (75 mg/kg/day) from the 11(th) to 17(th) day after infection caused significant decreases in worm burden (39%-61%) and egg production (42%-98%). Hz formation was significantly inhibited (40%-65%) in female worms recovered from QN- and QND-treated mice and correlated with reduction in the female worm burden. We also observed that QN treatment promoted remarkable ultrastructural changes in male and female worms, particularly in the gut epithelium and reduced the granulomatous reaction to parasite eggs trapped in the liver. Microarray gene expression analysis indicated that QN treatment increased the expression of transcripts related to musculature, protein synthesis and repair mechanisms. CONCLUSIONS: The overall significant reduction in several disease burden parameters by the antimalarial quinoline methanols indicates that interference with Hz formation in S. mansoni represents an important mechanism of schistosomicidal action of these compounds and points out the heme crystallization process as a valid chemotherapeutic target to treat schistosomiasis.
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spelling doaj.art-62d139d5534641b28986c39ac7bf0dac2022-12-21T18:19:56ZengPublic Library of Science (PLoS)PLoS Neglected Tropical Diseases1935-27352009-01-0137e47710.1371/journal.pntd.0000477Interference with hemozoin formation represents an important mechanism of schistosomicidal action of antimalarial quinoline methanols.Juliana B R Corrêa SoaresDiego MenezesMarcos A Vannier-SantosAntonio Ferreira-PereiraGiulliana T AlmeidaThiago M VenancioSergio Verjovski-AlmeidaVincent K ZishiriDavid KuterRoger HunterTimothy J EganMarcus F OliveiraBACKGROUND: The parasitic trematode Schistosoma mansoni is one of the major causative agents of human schistosomiasis, which afflicts 200 million people worldwide. Praziquantel remains the main drug used for schistosomiasis treatment, and reliance on the single therapy has been prompting the search for new therapeutic compounds against this disease. Our group has demonstrated that heme crystallization into hemozoin (Hz) within the S. mansoni gut is a major heme detoxification route with lipid droplets involved in this process and acting as a potential chemotherapeutical target. In the present work, we investigated the effects of three antimalarial compounds, quinine (QN), quinidine (QND) and quinacrine (QCR) in a murine schistosomiasis model by using a combination of biochemical, cell biology and molecular biology approaches. METHODOLOGY/PRINCIPAL FINDINGS: Treatment of S. mansoni-infected female Swiss mice with daily intraperitoneal injections of QN, and QND (75 mg/kg/day) from the 11(th) to 17(th) day after infection caused significant decreases in worm burden (39%-61%) and egg production (42%-98%). Hz formation was significantly inhibited (40%-65%) in female worms recovered from QN- and QND-treated mice and correlated with reduction in the female worm burden. We also observed that QN treatment promoted remarkable ultrastructural changes in male and female worms, particularly in the gut epithelium and reduced the granulomatous reaction to parasite eggs trapped in the liver. Microarray gene expression analysis indicated that QN treatment increased the expression of transcripts related to musculature, protein synthesis and repair mechanisms. CONCLUSIONS: The overall significant reduction in several disease burden parameters by the antimalarial quinoline methanols indicates that interference with Hz formation in S. mansoni represents an important mechanism of schistosomicidal action of these compounds and points out the heme crystallization process as a valid chemotherapeutic target to treat schistosomiasis.http://europepmc.org/articles/PMC2703804?pdf=render
spellingShingle Juliana B R Corrêa Soares
Diego Menezes
Marcos A Vannier-Santos
Antonio Ferreira-Pereira
Giulliana T Almeida
Thiago M Venancio
Sergio Verjovski-Almeida
Vincent K Zishiri
David Kuter
Roger Hunter
Timothy J Egan
Marcus F Oliveira
Interference with hemozoin formation represents an important mechanism of schistosomicidal action of antimalarial quinoline methanols.
PLoS Neglected Tropical Diseases
title Interference with hemozoin formation represents an important mechanism of schistosomicidal action of antimalarial quinoline methanols.
title_full Interference with hemozoin formation represents an important mechanism of schistosomicidal action of antimalarial quinoline methanols.
title_fullStr Interference with hemozoin formation represents an important mechanism of schistosomicidal action of antimalarial quinoline methanols.
title_full_unstemmed Interference with hemozoin formation represents an important mechanism of schistosomicidal action of antimalarial quinoline methanols.
title_short Interference with hemozoin formation represents an important mechanism of schistosomicidal action of antimalarial quinoline methanols.
title_sort interference with hemozoin formation represents an important mechanism of schistosomicidal action of antimalarial quinoline methanols
url http://europepmc.org/articles/PMC2703804?pdf=render
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