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Amaryllidaceae alkaloids with anti-Trypanosoma cruzi activity
BACKGROUND: Chagas disease, caused by the protozoan Trypanosoma cruzi, is a neglected disease that affects ~7 million people worldwide. Development of new drugs to treat the infection remains a priority since those currently available have frequent side effects and limited efficacy at the chronic st...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7288428/ https://www.ncbi.nlm.nih.gov/pubmed/32522289 http://dx.doi.org/10.1186/s13071-020-04171-6 |
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author | Martinez-Peinado, Nieves Cortes-Serra, Nuria Torras-Claveria, Laura Pinazo, Maria-Jesus Gascon, Joaquim Bastida, Jaume Alonso-Padilla, Julio |
author_facet | Martinez-Peinado, Nieves Cortes-Serra, Nuria Torras-Claveria, Laura Pinazo, Maria-Jesus Gascon, Joaquim Bastida, Jaume Alonso-Padilla, Julio |
author_sort | Martinez-Peinado, Nieves |
collection | PubMed |
description | BACKGROUND: Chagas disease, caused by the protozoan Trypanosoma cruzi, is a neglected disease that affects ~7 million people worldwide. Development of new drugs to treat the infection remains a priority since those currently available have frequent side effects and limited efficacy at the chronic stage. Natural products provide a pool of diversity structures to lead the chemical synthesis of novel molecules for this purpose. Herein we analyzed the anti-T. cruzi activity of nine alkaloids derived from plants of the family Amaryllidaceae. METHODS: The activity of each alkaloid was assessed by means of an anti-T. cruzi phenotypic assay. We further evaluated the compounds that inhibited parasite growth on two distinct cytotoxicity assays to discard those that were toxic to host cells and assure parasite selectivity. RESULTS: We identified a single compound (hippeastrine) that was selectively active against the parasite yielding selectivity indexes of 12.7 and 35.2 against Vero and HepG2 cells, respectively. Moreover, it showed specific activity against the amastigote stage (IC(50) = 3.31 μM). CONCLUSIONS: Results reported here suggest that natural products are an interesting source of new compounds for the development of drugs against Chagas disease. [Image: see text] |
format | Online Article Text |
id | pubmed-7288428 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-72884282020-06-11 Amaryllidaceae alkaloids with anti-Trypanosoma cruzi activity Martinez-Peinado, Nieves Cortes-Serra, Nuria Torras-Claveria, Laura Pinazo, Maria-Jesus Gascon, Joaquim Bastida, Jaume Alonso-Padilla, Julio Parasit Vectors Research BACKGROUND: Chagas disease, caused by the protozoan Trypanosoma cruzi, is a neglected disease that affects ~7 million people worldwide. Development of new drugs to treat the infection remains a priority since those currently available have frequent side effects and limited efficacy at the chronic stage. Natural products provide a pool of diversity structures to lead the chemical synthesis of novel molecules for this purpose. Herein we analyzed the anti-T. cruzi activity of nine alkaloids derived from plants of the family Amaryllidaceae. METHODS: The activity of each alkaloid was assessed by means of an anti-T. cruzi phenotypic assay. We further evaluated the compounds that inhibited parasite growth on two distinct cytotoxicity assays to discard those that were toxic to host cells and assure parasite selectivity. RESULTS: We identified a single compound (hippeastrine) that was selectively active against the parasite yielding selectivity indexes of 12.7 and 35.2 against Vero and HepG2 cells, respectively. Moreover, it showed specific activity against the amastigote stage (IC(50) = 3.31 μM). CONCLUSIONS: Results reported here suggest that natural products are an interesting source of new compounds for the development of drugs against Chagas disease. [Image: see text] BioMed Central 2020-06-10 /pmc/articles/PMC7288428/ /pubmed/32522289 http://dx.doi.org/10.1186/s13071-020-04171-6 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Martinez-Peinado, Nieves Cortes-Serra, Nuria Torras-Claveria, Laura Pinazo, Maria-Jesus Gascon, Joaquim Bastida, Jaume Alonso-Padilla, Julio Amaryllidaceae alkaloids with anti-Trypanosoma cruzi activity |
title | Amaryllidaceae alkaloids with anti-Trypanosoma cruzi activity |
title_full | Amaryllidaceae alkaloids with anti-Trypanosoma cruzi activity |
title_fullStr | Amaryllidaceae alkaloids with anti-Trypanosoma cruzi activity |
title_full_unstemmed | Amaryllidaceae alkaloids with anti-Trypanosoma cruzi activity |
title_short | Amaryllidaceae alkaloids with anti-Trypanosoma cruzi activity |
title_sort | amaryllidaceae alkaloids with anti-trypanosoma cruzi activity |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7288428/ https://www.ncbi.nlm.nih.gov/pubmed/32522289 http://dx.doi.org/10.1186/s13071-020-04171-6 |
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