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Ultrastructural alterations in Plasmodium falciparum induced by chalcone derivatives
OBJECTIVE: Chalcones (1, 3-diaryl-2-propen-1-ones) and their derivatives are widely explored from the past decade for its antimalarial activity. To elucidate their mechanism of action on the malaria parasite, the ultrastructural changes with the action of these derivatives in different organelles of...
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/PMC7296763/ https://www.ncbi.nlm.nih.gov/pubmed/32539868 http://dx.doi.org/10.1186/s13104-020-05132-z |
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author | Sinha, Shweta Radotra, B. D. Medhi, Bikash Batovska, Daniela I. Markova, Nadezhda Sehgal, Rakesh |
author_facet | Sinha, Shweta Radotra, B. D. Medhi, Bikash Batovska, Daniela I. Markova, Nadezhda Sehgal, Rakesh |
author_sort | Sinha, Shweta |
collection | PubMed |
description | OBJECTIVE: Chalcones (1, 3-diaryl-2-propen-1-ones) and their derivatives are widely explored from the past decade for its antimalarial activity. To elucidate their mechanism of action on the malaria parasite, the ultrastructural changes with the action of these derivatives in different organelles of the parasite were studied in vitro. Infected RBCs [CQ sensitive (MRC-2) and CQ resistant (RKL-9) Plasmodium strain] were treated with three chalcone derivatives 1, 2 and 3 and standard drugs, i.e., CQ and artemisinin at twice their respective IC(50) values for 24 h and then harvested, washed, fixed, embedded and stained to visualize ultra-structure changes before and after intervention of treatment under in vitro condition through transmission electron microscope. RESULTS: The ultrastructural changes demonstrate the significant disturbance of all parasite membranes, including those of the nucleus, mitochondria and food vacuole, in association with a marked reduction of ribosomes in the trophozoites and cessation of developing schizonts which suggest multiple mechanisms of action by which chalcone derivatives act on the malaria parasite. The present study opens up perspectives for further exploration of these derivatives in vivo malaria model to discover more about its effect and mechanism of action. |
format | Online Article Text |
id | pubmed-7296763 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-72967632020-06-16 Ultrastructural alterations in Plasmodium falciparum induced by chalcone derivatives Sinha, Shweta Radotra, B. D. Medhi, Bikash Batovska, Daniela I. Markova, Nadezhda Sehgal, Rakesh BMC Res Notes Research Note OBJECTIVE: Chalcones (1, 3-diaryl-2-propen-1-ones) and their derivatives are widely explored from the past decade for its antimalarial activity. To elucidate their mechanism of action on the malaria parasite, the ultrastructural changes with the action of these derivatives in different organelles of the parasite were studied in vitro. Infected RBCs [CQ sensitive (MRC-2) and CQ resistant (RKL-9) Plasmodium strain] were treated with three chalcone derivatives 1, 2 and 3 and standard drugs, i.e., CQ and artemisinin at twice their respective IC(50) values for 24 h and then harvested, washed, fixed, embedded and stained to visualize ultra-structure changes before and after intervention of treatment under in vitro condition through transmission electron microscope. RESULTS: The ultrastructural changes demonstrate the significant disturbance of all parasite membranes, including those of the nucleus, mitochondria and food vacuole, in association with a marked reduction of ribosomes in the trophozoites and cessation of developing schizonts which suggest multiple mechanisms of action by which chalcone derivatives act on the malaria parasite. The present study opens up perspectives for further exploration of these derivatives in vivo malaria model to discover more about its effect and mechanism of action. BioMed Central 2020-06-15 /pmc/articles/PMC7296763/ /pubmed/32539868 http://dx.doi.org/10.1186/s13104-020-05132-z 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 Note Sinha, Shweta Radotra, B. D. Medhi, Bikash Batovska, Daniela I. Markova, Nadezhda Sehgal, Rakesh Ultrastructural alterations in Plasmodium falciparum induced by chalcone derivatives |
title | Ultrastructural alterations in Plasmodium falciparum induced by chalcone derivatives |
title_full | Ultrastructural alterations in Plasmodium falciparum induced by chalcone derivatives |
title_fullStr | Ultrastructural alterations in Plasmodium falciparum induced by chalcone derivatives |
title_full_unstemmed | Ultrastructural alterations in Plasmodium falciparum induced by chalcone derivatives |
title_short | Ultrastructural alterations in Plasmodium falciparum induced by chalcone derivatives |
title_sort | ultrastructural alterations in plasmodium falciparum induced by chalcone derivatives |
topic | Research Note |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7296763/ https://www.ncbi.nlm.nih.gov/pubmed/32539868 http://dx.doi.org/10.1186/s13104-020-05132-z |
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