Plants of Brazilian restingas with tripanocide activity against Trypanosoma cruzi strains

被引:0
作者
Robson Xavier Faria
André Luis Almeida Souza
Barbara Lima
Luis Armando Candido Tietbohl
Caio Pinho Fernandes
Raquel Rodrigues Amaral
Bettina Monika Ruppelt
Marcelo Guerra Santos
Leandro Rocha
机构
[1] Laboratório de Toxoplasmose e outras Protozooses– Instituto Oswaldo Cruz,Laboratório de Tecnologia de Produtos Naturais
[2] Laboratório de Bioquímica de Peptídeos– Instituto Oswaldo Cruz, Departamento de Tecnologia Farmacêutica
[3] Universidade Federal Fluminense,Laboratório de Pesquisa em Fármacos – Departamento de Ciências Biológicas e da Saúde
[4] Universidade Federal do Amapá,Laboratório de Nanobiotecnologia Fitofarmacêutica – Curso de Ciências Farmacêuticas
[5] Universidade Federal do Amapá,Laboratório Universitário Rodolpho Albino – Pró
[6] Universidade Federal Fluminense,Reitoria de Extensão
[7] Universidade do Estado do Rio de Janeiro,Departamento de Ciências, Faculdade de Formação de Professores
来源
Journal of Bioenergetics and Biomembranes | 2017年 / 49卷
关键词
Brazilian; Restingas; Plants; Trypanocide;
D O I
暂无
中图分类号
学科分类号
摘要
Chagas disease is caused by the Trypanosoma cruzi affecting millions of people, and widespread throughout Latin America. This disease exhibits a problematic chemotherapy. Benznidazole, which is the drug currently used as standard treatment, lamentably evokes several adverse reactions. Among other options, natural products have been tested to discover a novel therapeutic drug for this disease. A lot of plants from the Brazilian flora did not contain studies about their biological effects. Restinga de Jurubatiba from Brazil is a sandbank ecosystem poorly studied in relation to plant biological activity. Thus, three plant species from Restinga de Jurubatiba were tested against in vitro antiprotozoal activity. Among six extracts obtained from leaves and stem parts and 2 essential oils derived from leave parts, only 3 extracts inhibited epimastigote proliferation. Substances present in the extracts with activity were isolated (quercetin, myricetin, and ursolic acid), and evaluated in relation to antiprotozoal activity against epimastigote Y and Dm28 Trypanosoma cruzi strains. All isolated substances were effective to reduce protozoal proliferation. Essentially, quercetin and myricetin did not cause mammalian cell toxicity. In summary, myricetin and quercetin molecule can be used as a scaffold to develop new effective drugs against Chagas’s disease.
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页码:473 / 483
页数:10
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