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(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

Therapeutic Effect of Diminazene Aceturate on Parasitic Blood Fluke Schistosoma mansoni Infection

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Author(s):
de Britto, Mariana G. [1] ; Mengarda, Ana C. [1] ; Oliveira, George L. [2] ; Cirino, Maria E. [1] ; Silva, Tais C. [1] ; de Oliveira, Rosimeire N. [3] ; Allegretti, Silmara M. [4] ; de Moraes, Josue [1]
Total Authors: 8
Affiliation:
[1] Univ Guarulhos, Nucleo Pesquisa Doencas Negligenciadas, Sao Paulo - Brazil
[2] Inst Fed Educ Ciencia & Tecnol Mato Grosso, Campus Avancado Guaranta do Norte, Guaranta Do Norte, Mato Grosso - Brazil
[3] Univ Estadual Ponta Grossa, Ponta Grossa, Parana - Brazil
[4] Univ Estadual Campinas, Campinas, SP - Brazil
Total Affiliations: 4
Document type: Journal article
Source: Antimicrobial Agents and Chemotherapy; v. 64, n. 11 NOV 2020.
Web of Science Citations: 0
Abstract

Praziquantel is currently the only drug available to treat schistosomiasis, a disease of enormous public health significance caused by a blood fluke of the genus Schistosoma. Diminazene, a drug approved by the FDA, has been successfully used to treat diseases caused by blood protozoan parasites. In this study, we evaluated the antiparasitic properties of diminazene against Schistosoma mansoni ex vivo and in mice harboring either chronic or early S. mansoni infections. In vitro, we monitored phenotypic and tegumental changes as well as the effects of the drug on pairing and egg production. In mice infected with either adult (chronic infection) or immature (early infection) worms, diminazene was administered intraperitoneally (10 to 100 mg/kg of body weight) or by oral gavage (100 to 400 mg/kg), and we studied the influence of the drug on worm burden and egg production. Liver and spleen pathologies and serum aminotransferase levels were also analyzed. In vitro, 50% effective concentrations (EC50) and EC90 revealed that diminazene is able to kill both immature and adult parasites, and its effect was time and concentration dependent. In addition, confocal laser scanning microscopy showed morphological alterations in the teguments of schistosomes. In an animal model, the influence of the drug on worm burden, egg production, hepatomegaly, and splenomegaly depended on the dosing regimen applied and the route of administration. Diminazene also caused a significant reduction in aminotransferase levels. Comparatively, diminazene treatment was more effective in chronic infection than in early infection. In tandem, our study revealed that diminazene possesses anthelmintic properties and inhibits liver injury caused by Schistosoma eggs. (AU)

FAPESP's process: 16/22488-3 - Drug repositioning for neglected diseases: identification of novel anthelmintic agents
Grantee:Josué de Moraes
Support Opportunities: Regular Research Grants