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Captopril reduces liver cytotoxicity in a murine model of Plasmodium chabaudi infection

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Autor(es):
Ventura, Priscilla Dantas de Souza ; de Souza, Daniel Vitor ; Aguiar, Anna Caroline C. ; Carvalho, Carolina P. F. ; Ribeiro, Daniel A. ; Nagaoka, Marcia R. ; Gazarini, Marcos L.
Número total de Autores: 7
Tipo de documento: Artigo Científico
Fonte: ENVIRONMENTAL TOXICOLOGY AND PHARMACOLOGY; v. 119, p. 8-pg., 2025-09-01.
Resumo

The genus Plasmodium is responsible for malaria infection and promoting an accumulation of hemozoin followed by the generation of oxidizing species in the liver that is involved in hepatic damage. In this context, we performed the histopathological analysis in the mice liver infected with Plasmodium chabaudi treated orally with the antimalarial chloroquine, captopril (ACE I inhibitor), losartan (AT1 receptor blocker). In hematoxylin and eosinstained liver sections, histopathological changes, such as sinusoid congestion, leukocyte infiltration, hemozoin deposition, portal tract inflammation, and metanuclear analysis were evaluated. The histopathological analysis shows a beneficial effect of chloroquine treatment alone or in combination with vasodilator treatments, reducing the score for each tissue change. Our data show that Plasmodium chabaudi infection compromises some hepatic histopathological parameters, and interestingly the treatment with vasodilators improved some of these alterations. Particularly, captopril reduces cytotoxicity induced by malaria infection in mouse liver cells. (AU)

Processo FAPESP: 17/00896-5 - Citoproteção hepática: da fibrose a isquemia e reperfusão
Beneficiário:Márcia Regina Nagaoka
Modalidade de apoio: Auxílio à Pesquisa - Regular
Processo FAPESP: 19/19708-0 - Identificação de novos compostos antimaláricos: uma estratégia multidisciplinar visando a busca por classes ativas contra novos alvos moleculares e diferentes estágios de vida do Plasmodium spp
Beneficiário:Anna Caroline Campos Aguiar
Modalidade de apoio: Auxílio à Pesquisa - Jovens Pesquisadores
Processo FAPESP: 09/54598-9 - Proteólise intracelular em parasitas da malária: caracterização e inibição de proteases em um novo ensaio para o ‘screening’ de drogas antimaláricas
Beneficiário:Marcos Leoni Gazarini Dutra
Modalidade de apoio: Auxílio à Pesquisa - Jovens Pesquisadores