Candimine from Hippeastrum escoipense (Amaryllidaceae): Anti-Trypanosoma cruzi activity and synergistic effect with benznidazole
- Autores
- Ortiz, Javier Esteban; Piñeiro Gomez, Mauricio Daniel; Martines Peinado, Nieves; Barrera, Patricia Andrea; Sosa, Miguel; Bastida, Jaume; Alonso Padilla, Julio; Feresin, Gabriela Egly
- Año de publicación
- 2023
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- Background: Chagas disease (CD), caused by Trypanosoma cruzi, represents a healththreat to around 20 million people worldwide. Side effects of benznidazole (Bzn)cause 15-20% of patients to discontinue their treatment. Evidence has increased infavour of the use of drug combinations to improve the efficacy and tolerance of thetreatment. Natural products are well known to provide structures that could serve asnew drugs or scaffolds for CD treatment. Spp of the Amaryllidoideae sub family ofAmaryllidaceae family are known by its bioactives alkaloids, which have a reportedantiparasitic activity.Purpose: To evaluate the anti-T. cruzi activity of the isolated alkaloid candimine(Cnd) from Hippeastrum escoipense Slanis & Huaylla; and to assess the combinationeffect between Cnd and Bzn against different life stages of T. cruzi parasites.Methods: The chemical profile of H. escoipense alkaloids extract (AE-H. escoipense),including quantitation of Cnd was performed through GC/MS and UPLC-MS/MStechniques. Subsequently, Cnd was isolated using Shephadex LH20. Then, the AE-H.escoipense and Cnd were tested against T. cruzi, (epimastigotes, trypomastigotes, andamastigotes) by in vitro proliferation and viability assays. The cytotoxicity wasevaluated against Vero and HepG2 mammalian cells. The ultrastructural analysis wasperform by Transmission Electron Microcopy (TEM) and mitochondrial activity wascarried out by MTT assay. Drug combination assay between Cnd and Bzn wasevaluated using the Chou-Talalay method.4Results: The AE-H. escoipense and Cnd showed high and specific anti-T. cruziactivity, comparable to Bzn. Cnd induces ultrastructural changes in T. cruzi, such asvacuolization, membrane blebs and increases the mitochondrial activity. Regarding,the interaction between Cnd and Bzn generates synergism in the combinations of0.25×IC50 in epimastigotes, 2×IC50 in trypomastigotes+amastigotes, and 0.25, 2, and4×IC50 in amastigotes.Conclusion: The synergism between Cnd and Bzn indicates that the combination atthe concentration of 4×IC50 could be useful as an effective new therapy against CD inthe chronic stage. Thus, Cnd isolated from the leaves of the H. escoipense emerges aspotential candidate for the development of a new drug for the treatment of CD.
Fil: Ortiz, Javier Esteban. Universidad Nacional de San Juan. Facultad de Ingeniería. Instituto de Biotecnología; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - San Juan; Argentina
Fil: Piñeiro Gomez, Mauricio Daniel. Universidad Nacional de San Juan. Facultad de Ingeniería. Instituto de Biotecnología; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - San Juan; Argentina
Fil: Martines Peinado, Nieves. Universidad de Barcelona; España
Fil: Barrera, Patricia Andrea. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mendoza. Instituto de Histología y Embriología de Mendoza Dr. Mario H. Burgos. Universidad Nacional de Cuyo. Facultad de Ciencias Médicas. Instituto de Histología y Embriología de Mendoza Dr. Mario H. Burgos; Argentina
Fil: Sosa, Miguel. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mendoza. Instituto de Histología y Embriología de Mendoza Dr. Mario H. Burgos. Universidad Nacional de Cuyo. Facultad de Ciencias Médicas. Instituto de Histología y Embriología de Mendoza Dr. Mario H. Burgos; Argentina
Fil: Bastida, Jaume. Universidad de Barcelona. Facultad de Farmacia; España
Fil: Alonso Padilla, Julio. Universidad de Barcelona; España
Fil: Feresin, Gabriela Egly. Universidad Nacional de San Juan. Facultad de Ingeniería. Instituto de Biotecnología; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - San Juan; Argentina - Materia
-
AMARYLLIDACEAE ALKALOIDS
CHAGAS DISEASE
ANTIPARASITIC ASSAYS
NEGLECTED DISEASE
CANDIMINE
TRYPANOSOMA CRUZI - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
- Repositorio
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/224977
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CONICET Digital (CONICET) |
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Candimine from Hippeastrum escoipense (Amaryllidaceae): Anti-Trypanosoma cruzi activity and synergistic effect with benznidazoleOrtiz, Javier EstebanPiñeiro Gomez, Mauricio DanielMartines Peinado, NievesBarrera, Patricia AndreaSosa, MiguelBastida, JaumeAlonso Padilla, JulioFeresin, Gabriela EglyAMARYLLIDACEAE ALKALOIDSCHAGAS DISEASEANTIPARASITIC ASSAYSNEGLECTED DISEASECANDIMINETRYPANOSOMA CRUZIhttps://purl.org/becyt/ford/1.4https://purl.org/becyt/ford/1Background: Chagas disease (CD), caused by Trypanosoma cruzi, represents a healththreat to around 20 million people worldwide. Side effects of benznidazole (Bzn)cause 15-20% of patients to discontinue their treatment. Evidence has increased infavour of the use of drug combinations to improve the efficacy and tolerance of thetreatment. Natural products are well known to provide structures that could serve asnew drugs or scaffolds for CD treatment. Spp of the Amaryllidoideae sub family ofAmaryllidaceae family are known by its bioactives alkaloids, which have a reportedantiparasitic activity.Purpose: To evaluate the anti-T. cruzi activity of the isolated alkaloid candimine(Cnd) from Hippeastrum escoipense Slanis & Huaylla; and to assess the combinationeffect between Cnd and Bzn against different life stages of T. cruzi parasites.Methods: The chemical profile of H. escoipense alkaloids extract (AE-H. escoipense),including quantitation of Cnd was performed through GC/MS and UPLC-MS/MStechniques. Subsequently, Cnd was isolated using Shephadex LH20. Then, the AE-H.escoipense and Cnd were tested against T. cruzi, (epimastigotes, trypomastigotes, andamastigotes) by in vitro proliferation and viability assays. The cytotoxicity wasevaluated against Vero and HepG2 mammalian cells. The ultrastructural analysis wasperform by Transmission Electron Microcopy (TEM) and mitochondrial activity wascarried out by MTT assay. Drug combination assay between Cnd and Bzn wasevaluated using the Chou-Talalay method.4Results: The AE-H. escoipense and Cnd showed high and specific anti-T. cruziactivity, comparable to Bzn. Cnd induces ultrastructural changes in T. cruzi, such asvacuolization, membrane blebs and increases the mitochondrial activity. Regarding,the interaction between Cnd and Bzn generates synergism in the combinations of0.25×IC50 in epimastigotes, 2×IC50 in trypomastigotes+amastigotes, and 0.25, 2, and4×IC50 in amastigotes.Conclusion: The synergism between Cnd and Bzn indicates that the combination atthe concentration of 4×IC50 could be useful as an effective new therapy against CD inthe chronic stage. Thus, Cnd isolated from the leaves of the H. escoipense emerges aspotential candidate for the development of a new drug for the treatment of CD.Fil: Ortiz, Javier Esteban. Universidad Nacional de San Juan. Facultad de Ingeniería. Instituto de Biotecnología; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - San Juan; ArgentinaFil: Piñeiro Gomez, Mauricio Daniel. Universidad Nacional de San Juan. Facultad de Ingeniería. Instituto de Biotecnología; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - San Juan; ArgentinaFil: Martines Peinado, Nieves. Universidad de Barcelona; EspañaFil: Barrera, Patricia Andrea. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mendoza. Instituto de Histología y Embriología de Mendoza Dr. Mario H. Burgos. Universidad Nacional de Cuyo. Facultad de Ciencias Médicas. Instituto de Histología y Embriología de Mendoza Dr. Mario H. Burgos; ArgentinaFil: Sosa, Miguel. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mendoza. Instituto de Histología y Embriología de Mendoza Dr. Mario H. Burgos. Universidad Nacional de Cuyo. Facultad de Ciencias Médicas. Instituto de Histología y Embriología de Mendoza Dr. Mario H. Burgos; ArgentinaFil: Bastida, Jaume. Universidad de Barcelona. Facultad de Farmacia; EspañaFil: Alonso Padilla, Julio. Universidad de Barcelona; EspañaFil: Feresin, Gabriela Egly. Universidad Nacional de San Juan. Facultad de Ingeniería. Instituto de Biotecnología; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - San Juan; ArgentinaElsevier Gmbh2023-03info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfapplication/pdfapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/224977Ortiz, Javier Esteban; Piñeiro Gomez, Mauricio Daniel; Martines Peinado, Nieves; Barrera, Patricia Andrea; Sosa, Miguel; et al.; Candimine from Hippeastrum escoipense (Amaryllidaceae): Anti-Trypanosoma cruzi activity and synergistic effect with benznidazole; Elsevier Gmbh; Phytomedicine; 114; 3-2023; 1-300944-7113CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/https://linkinghub.elsevier.com/retrieve/pii/S0944711323001496info:eu-repo/semantics/altIdentifier/doi/10.1016/j.phymed.2023.154788info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-03T09:51:50Zoai:ri.conicet.gov.ar:11336/224977instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-09-03 09:51:50.67CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
dc.title.none.fl_str_mv |
Candimine from Hippeastrum escoipense (Amaryllidaceae): Anti-Trypanosoma cruzi activity and synergistic effect with benznidazole |
title |
Candimine from Hippeastrum escoipense (Amaryllidaceae): Anti-Trypanosoma cruzi activity and synergistic effect with benznidazole |
spellingShingle |
Candimine from Hippeastrum escoipense (Amaryllidaceae): Anti-Trypanosoma cruzi activity and synergistic effect with benznidazole Ortiz, Javier Esteban AMARYLLIDACEAE ALKALOIDS CHAGAS DISEASE ANTIPARASITIC ASSAYS NEGLECTED DISEASE CANDIMINE TRYPANOSOMA CRUZI |
title_short |
Candimine from Hippeastrum escoipense (Amaryllidaceae): Anti-Trypanosoma cruzi activity and synergistic effect with benznidazole |
title_full |
Candimine from Hippeastrum escoipense (Amaryllidaceae): Anti-Trypanosoma cruzi activity and synergistic effect with benznidazole |
title_fullStr |
Candimine from Hippeastrum escoipense (Amaryllidaceae): Anti-Trypanosoma cruzi activity and synergistic effect with benznidazole |
title_full_unstemmed |
Candimine from Hippeastrum escoipense (Amaryllidaceae): Anti-Trypanosoma cruzi activity and synergistic effect with benznidazole |
title_sort |
Candimine from Hippeastrum escoipense (Amaryllidaceae): Anti-Trypanosoma cruzi activity and synergistic effect with benznidazole |
dc.creator.none.fl_str_mv |
Ortiz, Javier Esteban Piñeiro Gomez, Mauricio Daniel Martines Peinado, Nieves Barrera, Patricia Andrea Sosa, Miguel Bastida, Jaume Alonso Padilla, Julio Feresin, Gabriela Egly |
author |
Ortiz, Javier Esteban |
author_facet |
Ortiz, Javier Esteban Piñeiro Gomez, Mauricio Daniel Martines Peinado, Nieves Barrera, Patricia Andrea Sosa, Miguel Bastida, Jaume Alonso Padilla, Julio Feresin, Gabriela Egly |
author_role |
author |
author2 |
Piñeiro Gomez, Mauricio Daniel Martines Peinado, Nieves Barrera, Patricia Andrea Sosa, Miguel Bastida, Jaume Alonso Padilla, Julio Feresin, Gabriela Egly |
author2_role |
author author author author author author author |
dc.subject.none.fl_str_mv |
AMARYLLIDACEAE ALKALOIDS CHAGAS DISEASE ANTIPARASITIC ASSAYS NEGLECTED DISEASE CANDIMINE TRYPANOSOMA CRUZI |
topic |
AMARYLLIDACEAE ALKALOIDS CHAGAS DISEASE ANTIPARASITIC ASSAYS NEGLECTED DISEASE CANDIMINE TRYPANOSOMA CRUZI |
purl_subject.fl_str_mv |
https://purl.org/becyt/ford/1.4 https://purl.org/becyt/ford/1 |
dc.description.none.fl_txt_mv |
Background: Chagas disease (CD), caused by Trypanosoma cruzi, represents a healththreat to around 20 million people worldwide. Side effects of benznidazole (Bzn)cause 15-20% of patients to discontinue their treatment. Evidence has increased infavour of the use of drug combinations to improve the efficacy and tolerance of thetreatment. Natural products are well known to provide structures that could serve asnew drugs or scaffolds for CD treatment. Spp of the Amaryllidoideae sub family ofAmaryllidaceae family are known by its bioactives alkaloids, which have a reportedantiparasitic activity.Purpose: To evaluate the anti-T. cruzi activity of the isolated alkaloid candimine(Cnd) from Hippeastrum escoipense Slanis & Huaylla; and to assess the combinationeffect between Cnd and Bzn against different life stages of T. cruzi parasites.Methods: The chemical profile of H. escoipense alkaloids extract (AE-H. escoipense),including quantitation of Cnd was performed through GC/MS and UPLC-MS/MStechniques. Subsequently, Cnd was isolated using Shephadex LH20. Then, the AE-H.escoipense and Cnd were tested against T. cruzi, (epimastigotes, trypomastigotes, andamastigotes) by in vitro proliferation and viability assays. The cytotoxicity wasevaluated against Vero and HepG2 mammalian cells. The ultrastructural analysis wasperform by Transmission Electron Microcopy (TEM) and mitochondrial activity wascarried out by MTT assay. Drug combination assay between Cnd and Bzn wasevaluated using the Chou-Talalay method.4Results: The AE-H. escoipense and Cnd showed high and specific anti-T. cruziactivity, comparable to Bzn. Cnd induces ultrastructural changes in T. cruzi, such asvacuolization, membrane blebs and increases the mitochondrial activity. Regarding,the interaction between Cnd and Bzn generates synergism in the combinations of0.25×IC50 in epimastigotes, 2×IC50 in trypomastigotes+amastigotes, and 0.25, 2, and4×IC50 in amastigotes.Conclusion: The synergism between Cnd and Bzn indicates that the combination atthe concentration of 4×IC50 could be useful as an effective new therapy against CD inthe chronic stage. Thus, Cnd isolated from the leaves of the H. escoipense emerges aspotential candidate for the development of a new drug for the treatment of CD. Fil: Ortiz, Javier Esteban. Universidad Nacional de San Juan. Facultad de Ingeniería. Instituto de Biotecnología; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - San Juan; Argentina Fil: Piñeiro Gomez, Mauricio Daniel. Universidad Nacional de San Juan. Facultad de Ingeniería. Instituto de Biotecnología; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - San Juan; Argentina Fil: Martines Peinado, Nieves. Universidad de Barcelona; España Fil: Barrera, Patricia Andrea. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mendoza. Instituto de Histología y Embriología de Mendoza Dr. Mario H. Burgos. Universidad Nacional de Cuyo. Facultad de Ciencias Médicas. Instituto de Histología y Embriología de Mendoza Dr. Mario H. Burgos; Argentina Fil: Sosa, Miguel. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mendoza. Instituto de Histología y Embriología de Mendoza Dr. Mario H. Burgos. Universidad Nacional de Cuyo. Facultad de Ciencias Médicas. Instituto de Histología y Embriología de Mendoza Dr. Mario H. Burgos; Argentina Fil: Bastida, Jaume. Universidad de Barcelona. Facultad de Farmacia; España Fil: Alonso Padilla, Julio. Universidad de Barcelona; España Fil: Feresin, Gabriela Egly. Universidad Nacional de San Juan. Facultad de Ingeniería. Instituto de Biotecnología; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - San Juan; Argentina |
description |
Background: Chagas disease (CD), caused by Trypanosoma cruzi, represents a healththreat to around 20 million people worldwide. Side effects of benznidazole (Bzn)cause 15-20% of patients to discontinue their treatment. Evidence has increased infavour of the use of drug combinations to improve the efficacy and tolerance of thetreatment. Natural products are well known to provide structures that could serve asnew drugs or scaffolds for CD treatment. Spp of the Amaryllidoideae sub family ofAmaryllidaceae family are known by its bioactives alkaloids, which have a reportedantiparasitic activity.Purpose: To evaluate the anti-T. cruzi activity of the isolated alkaloid candimine(Cnd) from Hippeastrum escoipense Slanis & Huaylla; and to assess the combinationeffect between Cnd and Bzn against different life stages of T. cruzi parasites.Methods: The chemical profile of H. escoipense alkaloids extract (AE-H. escoipense),including quantitation of Cnd was performed through GC/MS and UPLC-MS/MStechniques. Subsequently, Cnd was isolated using Shephadex LH20. Then, the AE-H.escoipense and Cnd were tested against T. cruzi, (epimastigotes, trypomastigotes, andamastigotes) by in vitro proliferation and viability assays. The cytotoxicity wasevaluated against Vero and HepG2 mammalian cells. The ultrastructural analysis wasperform by Transmission Electron Microcopy (TEM) and mitochondrial activity wascarried out by MTT assay. Drug combination assay between Cnd and Bzn wasevaluated using the Chou-Talalay method.4Results: The AE-H. escoipense and Cnd showed high and specific anti-T. cruziactivity, comparable to Bzn. Cnd induces ultrastructural changes in T. cruzi, such asvacuolization, membrane blebs and increases the mitochondrial activity. Regarding,the interaction between Cnd and Bzn generates synergism in the combinations of0.25×IC50 in epimastigotes, 2×IC50 in trypomastigotes+amastigotes, and 0.25, 2, and4×IC50 in amastigotes.Conclusion: The synergism between Cnd and Bzn indicates that the combination atthe concentration of 4×IC50 could be useful as an effective new therapy against CD inthe chronic stage. Thus, Cnd isolated from the leaves of the H. escoipense emerges aspotential candidate for the development of a new drug for the treatment of CD. |
publishDate |
2023 |
dc.date.none.fl_str_mv |
2023-03 |
dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion http://purl.org/coar/resource_type/c_6501 info:ar-repo/semantics/articulo |
format |
article |
status_str |
publishedVersion |
dc.identifier.none.fl_str_mv |
http://hdl.handle.net/11336/224977 Ortiz, Javier Esteban; Piñeiro Gomez, Mauricio Daniel; Martines Peinado, Nieves; Barrera, Patricia Andrea; Sosa, Miguel; et al.; Candimine from Hippeastrum escoipense (Amaryllidaceae): Anti-Trypanosoma cruzi activity and synergistic effect with benznidazole; Elsevier Gmbh; Phytomedicine; 114; 3-2023; 1-30 0944-7113 CONICET Digital CONICET |
url |
http://hdl.handle.net/11336/224977 |
identifier_str_mv |
Ortiz, Javier Esteban; Piñeiro Gomez, Mauricio Daniel; Martines Peinado, Nieves; Barrera, Patricia Andrea; Sosa, Miguel; et al.; Candimine from Hippeastrum escoipense (Amaryllidaceae): Anti-Trypanosoma cruzi activity and synergistic effect with benznidazole; Elsevier Gmbh; Phytomedicine; 114; 3-2023; 1-30 0944-7113 CONICET Digital CONICET |
dc.language.none.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
info:eu-repo/semantics/altIdentifier/url/https://linkinghub.elsevier.com/retrieve/pii/S0944711323001496 info:eu-repo/semantics/altIdentifier/doi/10.1016/j.phymed.2023.154788 |
dc.rights.none.fl_str_mv |
info:eu-repo/semantics/openAccess https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
eu_rights_str_mv |
openAccess |
rights_invalid_str_mv |
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
dc.format.none.fl_str_mv |
application/pdf application/pdf application/pdf application/pdf application/pdf |
dc.publisher.none.fl_str_mv |
Elsevier Gmbh |
publisher.none.fl_str_mv |
Elsevier Gmbh |
dc.source.none.fl_str_mv |
reponame:CONICET Digital (CONICET) instname:Consejo Nacional de Investigaciones Científicas y Técnicas |
reponame_str |
CONICET Digital (CONICET) |
collection |
CONICET Digital (CONICET) |
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Consejo Nacional de Investigaciones Científicas y Técnicas |
repository.name.fl_str_mv |
CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas |
repository.mail.fl_str_mv |
dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar |
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1842269119932530688 |
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13.13397 |