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논문 기본 정보

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학술저널
저자정보
Felipe Finger Banfi (Universidade Federal de Mato Grosso) Karla de Sena Guedes (Universidade Federal de Mato Grosso) Carla Regina Andrighetti (Universidade Federal de Mato Grosso) Ana Carolina Aguiar (Universidade de São Paulo) Bryan Wender Debiasi (Universidade Federal de Mato Grosso) Janaina da Costa Noronha (Universidade Federal de Mato Grosso) Domingos de Jesus Rodrigues (Universidade Federal de Mato Grosso) Gerardo Magela Vieira Júnior (Universidade Federal do Piauí) Bruno Antonio Marinho Sanchez (Universidade Federal de Mato Grosso)
저널정보
대한기생충학열대의학회 Parasites, Hosts and Diseases The Korean Journal of Parasitology Vol.54 No.4
발행연도
2016.8
수록면
415 - 421 (7page)

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The drug-resistance of malaria parasites is the main problem in the disease control. The huge Brazilian biodiversity promotes the search for new compounds, where the animal kingdom is proving to be a promising source of bioactive compounds. The main objective of this study was to evaluate the antiplasmodial and cytotoxic activity of the compounds obtained from the toad venoms of Brazilian Amazon. Toad venoms were collected from the secretion of Rhinella marina and Rhaebo guttatus in Mato Grosso State, Brazil. The powder was extracted at room temperature, yielding 2 extracts (RG and RM) and a substance (‘1’) identified as a bufadienolide, named telocinobufagin. Growth inhibition, intraerythrocytic development, and parasite morphology were evaluated in culture by microscopic observations of Giemsastained thin blood films. Cytotoxicity was determined against HepG2 and BGM cells by MTT and neutral red assays. The 2 extracts and the pure substance (‘1’) tested were active against chloroquine-resistant Plasmodium falciparum strain, demonstrating lower IC50 values. In cytotoxic tests, the 2 extracts and substance ‘1’ showed pronounced lethal effects on chloroquine-resistant P. faciparum strain and low cytotoxic effect, highlighting toad parotoid gland secretions as a promising source of novel lead antiplasmodial compounds.

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Abstract
INTRODUCTION
MATERIALS AND METHODS
RESULTS
DISCUSSION
REFERENCES

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UCI(KEPA) : I410-ECN-0101-2017-513-001124511