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Acacia mangium: A promising plant for isolating anti-hepatitis C virus agents
Background: Medicinal plants are potential resources for isolating drug candidates. Various plants have been reported to possess pharmacological effects including anti-hepatitis C activities. The current study examined the anti-hepatitis C virus (HCV) activities of Acacia mangium extracts in solvent...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
F1000 Research Limited
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10690042/ https://www.ncbi.nlm.nih.gov/pubmed/38046541 http://dx.doi.org/10.12688/f1000research.124947.3 |
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author | Wahyuni, Tutik Sri Sukma, Nida S. Permanasari, Adita A. Aoki-Utsubo, Chie Widyawaruyanti, Aty Hafid, Achmad Fuad |
author_facet | Wahyuni, Tutik Sri Sukma, Nida S. Permanasari, Adita A. Aoki-Utsubo, Chie Widyawaruyanti, Aty Hafid, Achmad Fuad |
author_sort | Wahyuni, Tutik Sri |
collection | PubMed |
description | Background: Medicinal plants are potential resources for isolating drug candidates. Various plants have been reported to possess pharmacological effects including anti-hepatitis C activities. The current study examined the anti-hepatitis C virus (HCV) activities of Acacia mangium extracts in solvents with various polarities and further evaluated the mechanism of action of the extracts using Western blotting and combination treatment models. Methods: The leaves of A. mangium were extracted in two phases, first in ethanol and then in solvents with different polarities (n-hexane, dichloromethane, and methanol). HCV-infected Huh7it-1 cells were treated with the extracts at concentrations of 0.01, 0.1, 1, 10, 50, and 100 µg/mL. Results: The results revealed the strong anti-HCV activities of the extracts. The 50% inhibition concentrations (IC (50)s) of the ethanol, n-hexane, dichloromethane and methanol extracts were of 4.6 ± 0.3, 2.9 ± 0.2, 0.2 ± 0.3, and 2.8 ± 0.2 μg/mL, respectively, and no cytotoxic effect was detected. These extracts displayed stronger effects than the positive control ribavirin. The mode of action of the ethanol extract was evaluated at 30 µg/mL, revealing that the inhibitory effect was stronger on the post-entry step than on the entry step. Western blotting revealed that the extracts decreased NS3 protein expression, indicating that virus replication was suppressed. Further evaluation illustrated that combined treatment with the ethanol extract enhanced the anti-viral activity of simeprevir. Conclusions: These results indicated that A. mangium leaves could represent sources of anti-HCV agents. |
format | Online Article Text |
id | pubmed-10690042 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | F1000 Research Limited |
record_format | MEDLINE/PubMed |
spelling | pubmed-106900422023-12-02 Acacia mangium: A promising plant for isolating anti-hepatitis C virus agents Wahyuni, Tutik Sri Sukma, Nida S. Permanasari, Adita A. Aoki-Utsubo, Chie Widyawaruyanti, Aty Hafid, Achmad Fuad F1000Res Research Article Background: Medicinal plants are potential resources for isolating drug candidates. Various plants have been reported to possess pharmacological effects including anti-hepatitis C activities. The current study examined the anti-hepatitis C virus (HCV) activities of Acacia mangium extracts in solvents with various polarities and further evaluated the mechanism of action of the extracts using Western blotting and combination treatment models. Methods: The leaves of A. mangium were extracted in two phases, first in ethanol and then in solvents with different polarities (n-hexane, dichloromethane, and methanol). HCV-infected Huh7it-1 cells were treated with the extracts at concentrations of 0.01, 0.1, 1, 10, 50, and 100 µg/mL. Results: The results revealed the strong anti-HCV activities of the extracts. The 50% inhibition concentrations (IC (50)s) of the ethanol, n-hexane, dichloromethane and methanol extracts were of 4.6 ± 0.3, 2.9 ± 0.2, 0.2 ± 0.3, and 2.8 ± 0.2 μg/mL, respectively, and no cytotoxic effect was detected. These extracts displayed stronger effects than the positive control ribavirin. The mode of action of the ethanol extract was evaluated at 30 µg/mL, revealing that the inhibitory effect was stronger on the post-entry step than on the entry step. Western blotting revealed that the extracts decreased NS3 protein expression, indicating that virus replication was suppressed. Further evaluation illustrated that combined treatment with the ethanol extract enhanced the anti-viral activity of simeprevir. Conclusions: These results indicated that A. mangium leaves could represent sources of anti-HCV agents. F1000 Research Limited 2023-08-02 /pmc/articles/PMC10690042/ /pubmed/38046541 http://dx.doi.org/10.12688/f1000research.124947.3 Text en Copyright: © 2023 Wahyuni TS et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Wahyuni, Tutik Sri Sukma, Nida S. Permanasari, Adita A. Aoki-Utsubo, Chie Widyawaruyanti, Aty Hafid, Achmad Fuad Acacia mangium: A promising plant for isolating anti-hepatitis C virus agents |
title |
Acacia mangium: A promising plant for isolating anti-hepatitis C virus agents |
title_full |
Acacia mangium: A promising plant for isolating anti-hepatitis C virus agents |
title_fullStr |
Acacia mangium: A promising plant for isolating anti-hepatitis C virus agents |
title_full_unstemmed |
Acacia mangium: A promising plant for isolating anti-hepatitis C virus agents |
title_short |
Acacia mangium: A promising plant for isolating anti-hepatitis C virus agents |
title_sort | acacia mangium: a promising plant for isolating anti-hepatitis c virus agents |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10690042/ https://www.ncbi.nlm.nih.gov/pubmed/38046541 http://dx.doi.org/10.12688/f1000research.124947.3 |
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