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Immunomodulatory Effects of Asiaticoside Against Shigella flexneri-Infected Macrophages
Macrophages provide the first line of defense against Shigella flexneri infection in the gastrointestinal tract by inducing a variety of inflammatory and antimicrobial responses. Secondary metabolites of plants are used as drugs against infections that are resistant to common antibiotics. In this st...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Penerbit Universiti Sains Malaysia
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8300950/ https://www.ncbi.nlm.nih.gov/pubmed/34367513 http://dx.doi.org/10.21315/tlsr2021.32.2.3 |
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author | Michael, Shalini Zakaria, Nor Munirah Abbas, Muhammad Adamu Abdullah, Hasmah Suppian, Rapeah |
author_facet | Michael, Shalini Zakaria, Nor Munirah Abbas, Muhammad Adamu Abdullah, Hasmah Suppian, Rapeah |
author_sort | Michael, Shalini |
collection | PubMed |
description | Macrophages provide the first line of defense against Shigella flexneri infection in the gastrointestinal tract by inducing a variety of inflammatory and antimicrobial responses. Secondary metabolites of plants are used as drugs against infections that are resistant to common antibiotics. In this study, the innate effects of asiaticoside on the proinflammatory activity of mouse macrophages infected with S. flexneri were investigated. The viability of the infected mouse macrophages were examined using viability assay, while the pro-inflammatory cytokines productions were determined using the enzyme-linked immunosorbent assay (ELISA) for determination of IL-1β, IL-12 p40 and TNF-α levels. The production of nitric oxide (NO) and the expression of inducible nitric oxide synthase (iNOS) protein were determined using the Griess assay and western blot, respectively. Statistical analyses were performed using the Statistical Package of Social Sciences (SPSS) software, version 20. The data obtained from independent experiments (n = 3) were presented as the mean ± standard error of mean (SEM). The results showed that, asiaticoside stimulated the infected macrophages by stimulating increased production of TNF-α, IL-12 p40 and NO as well as increased expression of iNOS in a dose-dependent manner. In contrast the viability of the cells and the production of IL-1β and were reduced also in a dose-dependent manner when compared to untreated cells. These results indicate that asiaticoside has immunomodulatory effects on the innate immune function of infected macrophages, showing the potential use of this compound to reduce the clinical symptoms of the infections. |
format | Online Article Text |
id | pubmed-8300950 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Penerbit Universiti Sains Malaysia |
record_format | MEDLINE/PubMed |
spelling | pubmed-83009502021-08-05 Immunomodulatory Effects of Asiaticoside Against Shigella flexneri-Infected Macrophages Michael, Shalini Zakaria, Nor Munirah Abbas, Muhammad Adamu Abdullah, Hasmah Suppian, Rapeah Trop Life Sci Res Article Macrophages provide the first line of defense against Shigella flexneri infection in the gastrointestinal tract by inducing a variety of inflammatory and antimicrobial responses. Secondary metabolites of plants are used as drugs against infections that are resistant to common antibiotics. In this study, the innate effects of asiaticoside on the proinflammatory activity of mouse macrophages infected with S. flexneri were investigated. The viability of the infected mouse macrophages were examined using viability assay, while the pro-inflammatory cytokines productions were determined using the enzyme-linked immunosorbent assay (ELISA) for determination of IL-1β, IL-12 p40 and TNF-α levels. The production of nitric oxide (NO) and the expression of inducible nitric oxide synthase (iNOS) protein were determined using the Griess assay and western blot, respectively. Statistical analyses were performed using the Statistical Package of Social Sciences (SPSS) software, version 20. The data obtained from independent experiments (n = 3) were presented as the mean ± standard error of mean (SEM). The results showed that, asiaticoside stimulated the infected macrophages by stimulating increased production of TNF-α, IL-12 p40 and NO as well as increased expression of iNOS in a dose-dependent manner. In contrast the viability of the cells and the production of IL-1β and were reduced also in a dose-dependent manner when compared to untreated cells. These results indicate that asiaticoside has immunomodulatory effects on the innate immune function of infected macrophages, showing the potential use of this compound to reduce the clinical symptoms of the infections. Penerbit Universiti Sains Malaysia 2021-06 2021-06-29 /pmc/articles/PMC8300950/ /pubmed/34367513 http://dx.doi.org/10.21315/tlsr2021.32.2.3 Text en © Penerbit Universiti Sains Malaysia, 2021 https://creativecommons.org/licenses/by/4.0/This work is licensed under the terms of the Creative Commons Attribution (CC BY) (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ). |
spellingShingle | Article Michael, Shalini Zakaria, Nor Munirah Abbas, Muhammad Adamu Abdullah, Hasmah Suppian, Rapeah Immunomodulatory Effects of Asiaticoside Against Shigella flexneri-Infected Macrophages |
title | Immunomodulatory Effects of Asiaticoside Against Shigella flexneri-Infected Macrophages |
title_full | Immunomodulatory Effects of Asiaticoside Against Shigella flexneri-Infected Macrophages |
title_fullStr | Immunomodulatory Effects of Asiaticoside Against Shigella flexneri-Infected Macrophages |
title_full_unstemmed | Immunomodulatory Effects of Asiaticoside Against Shigella flexneri-Infected Macrophages |
title_short | Immunomodulatory Effects of Asiaticoside Against Shigella flexneri-Infected Macrophages |
title_sort | immunomodulatory effects of asiaticoside against shigella flexneri-infected macrophages |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8300950/ https://www.ncbi.nlm.nih.gov/pubmed/34367513 http://dx.doi.org/10.21315/tlsr2021.32.2.3 |
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