Trypanocidal activity of polysaccharide extract from Genipa americana leaves

被引:19
|
作者
da Silva Souza, Racquel Oliveira [1 ]
Sousa, Paloma Ledo [1 ]
Pessoa Bezerra de Menezes, Ramon Roseo Paula [2 ]
Sampaio, Tiago Lima [2 ]
Tessarolo, Louise Donadello [1 ]
Oliveira Silva, Francisca Crislandia [3 ]
Pereira, Maria Goncalves [3 ]
Costa Martins, Alice Maria [1 ]
机构
[1] Univ Fed Ceara, Dept Anal Clin & Toxicol, Fortaleza, Ceara, Brazil
[2] Univ Fed Ceara, Dept Fisiol & Farmacol, Fortaleza, Ceara, Brazil
[3] Univ Estadual Ceara, Fac Educ Ciencias & Letras Sertao Cent, Quixada, Ceara, Brazil
关键词
Plant polysaccharide; Genipa americana; Trypanosoma cruzi; Necrosis; Reactive oxygen species; TRYPANOSOMA-CRUZI ACTIVITY; IN-VITRO; ANTIPARASITIC ACTIVITY; PLANTS; FRACTIONS; BARKS;
D O I
10.1016/j.jep.2017.08.042
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Ethnopharmacological relevance: The parts of the Genipa americana (Rubiaceae) tree, also known as "jenipapo" or "jenipapeiro", has been used in traditional Medicine in parasitic and bacterial infections. Thus, the experimental evolution of the antiparasitic activity of polysaccharide extracts from Genipa americana leaves, and correlation with antiparasitic and popular use is important. Aim of the study: To evaluate the effect of polysaccharide extract obtained from Genipa americana leaves on all Trypanosoma cruzi (Y strain: benznidazole-resistant) developmental forms, a protozoan that causes Chagas' disease. Materials and methods: An extract rich in polysaccharides was obtained from the leaves of Genipa americana (GaEPL) by associating depigmentation in methanol followed by extraction of polysaccharides in NaOH and precipitation with ethanol. Cytotoxicity to mammalian cells (LLC-MK2) was determined using an MTT assay. Antiparasitic activity was evaluated against epimastigote, trypomastighe and amastigote forms of T. cruzi. Cell death mechanism was determined in epimastigote forms by flow cytometry analysis after FITC-annexin V (Ax), 7-AAD, and H2DCFDA staining. Striking morphological changes were observed by scanning electron microscope. Results: GaEPL (6.5% yield; 54.6% total carbohydrate; 21.1% uronic acid and 12% protein), inhibited all T. cruzi developmental forms, epimastigotes after periods of 24 h (IC50 = 740 +/- 0.075 mu g/mL), 48 h (lC(50) = 710 +/- 0.053 mu g/mL) and 72 h (IC50 = 870 +/- 0.052 mu g/mL) of incubation; trypomastigotes (IC50 = 470 +/- 0.082 mu g/mL) after periods of 24 h and intracellular amastigotes (IC50/2 = 235 or IC50 = 470 mu g/mL) after periods of 24 and 48 h of incubation, with no toxicity on LLC-MK2 cells at the used concentrations. Analysis of the possible action mechanism in the parasites suggested cell death by necrosis with the involvement of reactive oxygen species (ROS). The scanning electron microscopy (SEM) confirmed T. cruzi death by necrosis. Conclusions: GaEPL showed significant activity against the epimastigote, trypomastigote and amastigote forms of T. cruzi, strain Y, suggesting cell death by necrosis with involvement of reactive oxygen species.
引用
收藏
页码:311 / 317
页数:7
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