dc.creatorSpina Zapata, Renata María
dc.creatorLozano, Esteban Sebastián
dc.creatorBarrera, Patricia Andrea
dc.creatorAgüero, María Belén
dc.creatorTapia, Aníbal Alejandro
dc.creatorFeresin, Gabriela Egly
dc.creatorSosa Escudero, Miguel Angel
dc.date.accessioned2020-01-02T20:38:46Z
dc.date.accessioned2022-10-15T16:20:27Z
dc.date.available2020-01-02T20:38:46Z
dc.date.available2022-10-15T16:20:27Z
dc.date.created2020-01-02T20:38:46Z
dc.date.issued2018-07
dc.identifierSpina Zapata, Renata María; Lozano, Esteban Sebastián; Barrera, Patricia Andrea; Agüero, María Belén; Tapia, Aníbal Alejandro; et al.; Antiproliferative effect and ultrastructural alterations induced by 5-O-methylembelin on Trypanosoma cruzi; Elsevier Gmbh; Phytomedicine; 46; 7-2018; 111-118
dc.identifier0944-7113
dc.identifierhttp://hdl.handle.net/11336/93309
dc.identifierCONICET Digital
dc.identifierCONICET
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/4408377
dc.description.abstractBackground: Embelin (EMB), obtained from Oxalis erythrorhiza Gillies ex Hooker et Arnott (Oxalidaceae), was reported against Trypanosoma cruzi and Leishmania spp. Additionally, antiprotozoan activity against Plasmodium falciparum was reported for its methylated derivative (ME). Purpose: To evaluate the potential anti-Trypanosoma cruzi activity of EMB, ME and 2,5-di-O-methylembelin (DME) and analyze the possible mechanism of action. Study design/Methods: EMB was isolated by a chromatographic method from the air-dried ground whole plant. To evaluate the effects of methylation, ME and DME were synthesized and tested against T. cruzi epimastigotes and trypomastigotes. The most active compound ME was evaluated against amastigotes. Ultrastructural alterations, ROS generation and the effect on mitochondrial activity of ME were measured. Results: Compounds inhibited the proliferation of epimastigotes. ME was also active against intracellular amastigotes. Mitochondrial alterations were observed by TEM. Additionally, ME modified the mitochondrial activity, and induced an increase in ROS levels. These evidences postulate the mitochondrion as a possible target of ME. Conclusion: ME inhibited amastigotes proliferation, thus being a potential lead compound for the treatment of Chagas’ disease.
dc.languageeng
dc.publisherElsevier Gmbh
dc.relationinfo:eu-repo/semantics/altIdentifier/url/https://www.sciencedirect.com/science/article/pii/S0944711318301326
dc.relationinfo:eu-repo/semantics/altIdentifier/doi/https://doi.org/10.1016/j.phymed.2018.04.032
dc.rightshttps://creativecommons.org/licenses/by-nc-nd/2.5/ar/
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subject2,5-DI-O-METHYLEMBELIN (DME)
dc.subject5-O-METHYLEMBELIN (ME)
dc.subjectCHAGAS' DISEASE
dc.subjectEMBELIN (EMB)
dc.subjectTRYPANOSOMA CRUZI
dc.titleAntiproliferative effect and ultrastructural alterations induced by 5-O-methylembelin on Trypanosoma cruzi
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:ar-repo/semantics/artículo
dc.typeinfo:eu-repo/semantics/publishedVersion


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