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Inhibition of Plasmodium Liver Infection by Ivermectin
Avermectins are powerful endectocides with an established potential to reduce the incidence of vector-borne diseases. Here, we show that several avermectins inhibit the hepatic stage of Plasmodium infection in vitro. Notably, ivermectin potently inhibits liver infection in vivo by impairing parasite...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Microbiology
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5278742/ https://www.ncbi.nlm.nih.gov/pubmed/27895022 http://dx.doi.org/10.1128/AAC.02005-16 |
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author | Mendes, António M. Albuquerque, Inês S. Machado, Marta Pissarra, Joana Meireles, Patrícia Prudêncio, Miguel |
author_facet | Mendes, António M. Albuquerque, Inês S. Machado, Marta Pissarra, Joana Meireles, Patrícia Prudêncio, Miguel |
author_sort | Mendes, António M. |
collection | PubMed |
description | Avermectins are powerful endectocides with an established potential to reduce the incidence of vector-borne diseases. Here, we show that several avermectins inhibit the hepatic stage of Plasmodium infection in vitro. Notably, ivermectin potently inhibits liver infection in vivo by impairing parasite development inside hepatocytes. This impairment has a clear impact on the ensuing blood stage parasitemia, reducing disease severity and enhancing host survival. Ivermectin has been proposed as a tool to control malaria transmission because of its effects on the mosquito vector. Our study extends the effect of ivermectin to the early stages of mammalian host infection and supports the inclusion of this multipurpose drug in malaria control strategies. |
format | Online Article Text |
id | pubmed-5278742 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | American Society for Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-52787422017-02-06 Inhibition of Plasmodium Liver Infection by Ivermectin Mendes, António M. Albuquerque, Inês S. Machado, Marta Pissarra, Joana Meireles, Patrícia Prudêncio, Miguel Antimicrob Agents Chemother Experimental Therapeutics Avermectins are powerful endectocides with an established potential to reduce the incidence of vector-borne diseases. Here, we show that several avermectins inhibit the hepatic stage of Plasmodium infection in vitro. Notably, ivermectin potently inhibits liver infection in vivo by impairing parasite development inside hepatocytes. This impairment has a clear impact on the ensuing blood stage parasitemia, reducing disease severity and enhancing host survival. Ivermectin has been proposed as a tool to control malaria transmission because of its effects on the mosquito vector. Our study extends the effect of ivermectin to the early stages of mammalian host infection and supports the inclusion of this multipurpose drug in malaria control strategies. American Society for Microbiology 2017-01-24 /pmc/articles/PMC5278742/ /pubmed/27895022 http://dx.doi.org/10.1128/AAC.02005-16 Text en Copyright © 2017 Mendes et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (http://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Experimental Therapeutics Mendes, António M. Albuquerque, Inês S. Machado, Marta Pissarra, Joana Meireles, Patrícia Prudêncio, Miguel Inhibition of Plasmodium Liver Infection by Ivermectin |
title | Inhibition of Plasmodium Liver Infection by Ivermectin |
title_full | Inhibition of Plasmodium Liver Infection by Ivermectin |
title_fullStr | Inhibition of Plasmodium Liver Infection by Ivermectin |
title_full_unstemmed | Inhibition of Plasmodium Liver Infection by Ivermectin |
title_short | Inhibition of Plasmodium Liver Infection by Ivermectin |
title_sort | inhibition of plasmodium liver infection by ivermectin |
topic | Experimental Therapeutics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5278742/ https://www.ncbi.nlm.nih.gov/pubmed/27895022 http://dx.doi.org/10.1128/AAC.02005-16 |
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