In vitro and in vivo antiparasitic activity of Physalis angulata L. concentrated ethanolic extract against Trypanosoma cruzi

被引:32
|
作者
Meira, Cassio Santana [1 ]
Guimaraes, Elisalva Teixeira [1 ,2 ]
Ferreira dos Santos, Jamyle Andrade [1 ,2 ]
Magalhaes Moreira, Diogo Rodrigo [1 ]
Nogueira, Renata Campos [1 ]
Barbosa Tomassini, Therezinha Coelho [3 ]
Ribeiro, Ivone Maria [3 ]
Campos de Souza, Claudia Valeria [3 ]
dos Santos, Ricardo Ribeiro [4 ]
Pereira Soares, Milena Botelho [1 ,4 ]
机构
[1] Fundacao Oswaldo Cruz, Ctr Pesquisas Goncalo Moniz, BR-40296710 Salvador, BA, Brazil
[2] Univ Estado Bahia, Salvador, BA, Brazil
[3] Farmanguinhos Fiocruz, Lab Quim Prod Nat Extracao Isolamento & Purificac, Rio De Janeiro, RJ, Brazil
[4] Hosp Sao Rafael, Ctr Biotecnol & Terapia Celular, Salvador, BA, Brazil
关键词
Chagas disease; Trypanosoma cruzi; Physalis angulata; Plant extract; Drug combination; NATURAL-PRODUCTS; CHAGAS-DISEASE; MODE;
D O I
10.1016/j.phymed.2015.07.004
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Background: The current treatment of Chagas disease, endemic in Latin America and emerging in several countries, is limited by the frequent side effects and variable efficacy of benznidazole. Natural products are an important source for the search for new drugs. Aim/hypothesis: Considering the great potential of natural products as antiparasitic agents, we investigated the anti-Ttypanosoma cruzi activity of a concentrated ethanolic extract of Physalis angulata (EEPA). Methods: Cytotoxicity to mammalian cells was determined using mouse peritoneal macrophages. The antiparasitic activity was evaluated against axenic epimastigote and bloodstream trypomastigote forms of T. cruzi, and against amastigote forms using T. cruzi-infected macrophages. Cell death mechanism was determined in trypomastigotes by flow cytometry analysis after annexin V and propidium iodide staining. The efficacy of EEPA was examined in vivo in an acute model of infection by monitoring blood parasitaemia and survival rate 30 days after treatment. The effect against trypomastigotes of EEPA and benznidazole acting in combination was evaluated. Results: EEPA effectively inhibits the epimastigote growth (IC50 2.9 +/- 0.1 mu M) and reduces bloodstream trypomastigote viability (EC50 1.7 +/- 0.5 mu M). It causes parasite cell death by necrosis. EEPA impairs parasite infectivity as well as amastigote development in concentrations noncytotoxic to mammalian cells. In mice acutely-infected with T. cruzi, EEPA reduced the blood parasitaemia in 72.7%. When combined with benznidazole, EEPA showed a synergistic anti-T. cruzi activity, displaying CI values of 0.8 +/- 0.07 at EC50 and 0.83 +/- 0.1 at EC90. Conclusion: EEPA has antiparasitic activity against T. cruzi, causing cell death by necrosis and showing synergistic activity with benznidazole. These findings were reinforced by the observed efficacy of EEPA in reducing parasite load in T. cruzi-mice. Therefore, this represents an important source of antiparasitic natural products. (C) 2015 Elsevier GmbH. All rights reserved.
引用
收藏
页码:969 / 974
页数:6
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