In vitro activity and cell death mechanism induced by acrylonitrile derivatives against Leishmania amazonensis
Leishmaniasis produces approximately-one million of new cases annually, making it one of the most important tropical diseases. As current treatments are not fully effective and are toxic, it is necessary to develop new therapies that are more effective and less toxic, and cause a controlled cell death, with which we can avoid the immunological problems caused by necrosis. In this work 32 acrylonitriles were studied in vitro against Leishmania amazonensis. Three compounds Q20 (12.41), Q29 (11.2) and Q31 (11.56) had better selectivity than the reference compound, miltefosine (11.14) against promastigotes of these parasites, for this reason they were selected to determine their mechanism of action to know the cell death type of they produce. The results of the mechanisms of action show that these three acrylonitriles tested produce chromatin condensation, decreased mitochondrial membrane potential, altered plasma permeability and production of reactive oxygen species. All these characteristic events seem to indicate programmed cell death. Therefore, this study demonstrates the activity of acrylonitriles derivatives as possible leishmanicidal agents.
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Elsevier BV
2022-05-15
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Subjects: | Chemotherapy, leishmania, acrylonitrile, toxicity, amazonensis, |
Online Access: | http://hdl.handle.net/10261/298809 |
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dig-ipna-es-10261-2988092023-03-13T10:02:25Z In vitro activity and cell death mechanism induced by acrylonitrile derivatives against Leishmania amazonensis Bethencourt-Estrella, Carlos J. Delgado-Hernández, Samuel López-Arencibia, Atteneri San Nicolás-Hernández, Desirée Tejedor, David García-Tellado, Fernando Lorenzo-Morales, Jacob Piñero, José E. Instituto de Salud Carlos III Red de Investigación Cooperativa en Enfermedades Tropicales (España) Centro de Investigación Biomédica en Red de Enfermedades Infecciosas (España) Cabildo de Tenerife Ministerio de Ciencia, Innovación y Universidades (España) Agencia Estatal de Investigación (España) European Commission Agencia Canaria de Investigación, Innovación y Sociedad de la Información Chemotherapy leishmania acrylonitrile toxicity amazonensis Leishmaniasis produces approximately-one million of new cases annually, making it one of the most important tropical diseases. As current treatments are not fully effective and are toxic, it is necessary to develop new therapies that are more effective and less toxic, and cause a controlled cell death, with which we can avoid the immunological problems caused by necrosis. In this work 32 acrylonitriles were studied in vitro against Leishmania amazonensis. Three compounds Q20 (12.41), Q29 (11.2) and Q31 (11.56) had better selectivity than the reference compound, miltefosine (11.14) against promastigotes of these parasites, for this reason they were selected to determine their mechanism of action to know the cell death type of they produce. The results of the mechanisms of action show that these three acrylonitriles tested produce chromatin condensation, decreased mitochondrial membrane potential, altered plasma permeability and production of reactive oxygen species. All these characteristic events seem to indicate programmed cell death. Therefore, this study demonstrates the activity of acrylonitriles derivatives as possible leishmanicidal agents. This work was funded by PI18/01380 from the Instituto de Salud Carlos III, Spain; RICET (project RD16/0027/0001) from the Programa Redes Temáticas de Investigación Cooperativa, FIS (Ministerio Español de Salud, Madrid, Spain); CB21/13/00100 Consorcio Centro De Investigación Biomédica En Red M.P. (CIBER) de Enfermedades Infecciosas, Inst. de Salud Carlos III, Madrid, Spain and Cabildo de Tenerife, MEDI and FDCAN and Spanish Ministry of Science, Innovation and Universities (MICINN), State Research Agency (AEI) and the European Regional Development Funds (ERDF) (21/0587). Spanish Ministry of Science, Innovation and Universities (MICINN), State Research Agency (AEI), the European Regional Development Funds (ERDF) (PGC2018–094503-B-C21), C.J.B.-E. (TESIS2020010057) and D.S.N.-H. (TESIS2019010065) was funded by a grant from the Agencia Canaria de Investigación, Innovación y Sociedad de la Información cofunded by FEDER. S.D.-H thanks La Laguna University and Ministry of Science and Innovation for a Junior Posdoctoral contract. Peer reviewed 2023-03-13T10:02:25Z 2023-03-13T10:02:25Z 2022-05-15 artículo Bioorganic Chemistry, 124: 1-12 (2022) 0045-2068 http://hdl.handle.net/10261/298809 10.1016/j.bioorg.2022.105872 1090-2120 en #PLACEHOLDER_PARENT_METADATA_VALUE# info:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2017-2020/PGC2018-094503-B-C21/ES/QUIMICA SOSTENIBLE: DE MOLECULAS PEQUEÑAS A SISTEMAS FUNCIONALES COMPLEJOS/ Publisher's version https://doi.org/10.1016/j.bioorg.2022.105872 Sí open Elsevier BV |
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Chemotherapy leishmania acrylonitrile toxicity amazonensis Chemotherapy leishmania acrylonitrile toxicity amazonensis |
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Chemotherapy leishmania acrylonitrile toxicity amazonensis Chemotherapy leishmania acrylonitrile toxicity amazonensis Bethencourt-Estrella, Carlos J. Delgado-Hernández, Samuel López-Arencibia, Atteneri San Nicolás-Hernández, Desirée Tejedor, David García-Tellado, Fernando Lorenzo-Morales, Jacob Piñero, José E. In vitro activity and cell death mechanism induced by acrylonitrile derivatives against Leishmania amazonensis |
description |
Leishmaniasis produces approximately-one million of new cases annually, making it one of the most important tropical diseases. As current treatments are not fully effective and are toxic, it is necessary to develop new therapies that are more effective and less toxic, and cause a controlled cell death, with which we can avoid the immunological problems caused by necrosis. In this work 32 acrylonitriles were studied in vitro against Leishmania amazonensis. Three compounds Q20 (12.41), Q29 (11.2) and Q31 (11.56) had better selectivity than the reference compound, miltefosine (11.14) against promastigotes of these parasites, for this reason they were selected to determine their mechanism of action to know the cell death type of they produce. The results of the mechanisms of action show that these three acrylonitriles tested produce chromatin condensation, decreased mitochondrial membrane potential, altered plasma permeability and production of reactive oxygen species. All these characteristic events seem to indicate programmed cell death. Therefore, this study demonstrates the activity of acrylonitriles derivatives as possible leishmanicidal agents. |
author2 |
Instituto de Salud Carlos III |
author_facet |
Instituto de Salud Carlos III Bethencourt-Estrella, Carlos J. Delgado-Hernández, Samuel López-Arencibia, Atteneri San Nicolás-Hernández, Desirée Tejedor, David García-Tellado, Fernando Lorenzo-Morales, Jacob Piñero, José E. |
format |
artículo |
topic_facet |
Chemotherapy leishmania acrylonitrile toxicity amazonensis |
author |
Bethencourt-Estrella, Carlos J. Delgado-Hernández, Samuel López-Arencibia, Atteneri San Nicolás-Hernández, Desirée Tejedor, David García-Tellado, Fernando Lorenzo-Morales, Jacob Piñero, José E. |
author_sort |
Bethencourt-Estrella, Carlos J. |
title |
In vitro activity and cell death mechanism induced by acrylonitrile derivatives against Leishmania amazonensis |
title_short |
In vitro activity and cell death mechanism induced by acrylonitrile derivatives against Leishmania amazonensis |
title_full |
In vitro activity and cell death mechanism induced by acrylonitrile derivatives against Leishmania amazonensis |
title_fullStr |
In vitro activity and cell death mechanism induced by acrylonitrile derivatives against Leishmania amazonensis |
title_full_unstemmed |
In vitro activity and cell death mechanism induced by acrylonitrile derivatives against Leishmania amazonensis |
title_sort |
in vitro activity and cell death mechanism induced by acrylonitrile derivatives against leishmania amazonensis |
publisher |
Elsevier BV |
publishDate |
2022-05-15 |
url |
http://hdl.handle.net/10261/298809 |
work_keys_str_mv |
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