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Microbicide Containing Ellagic Acid Can Inhibit HIV-1 Infection
Objectives: Ellagic acid (EA) has a wide range of biological effects. The purpose of this study was to investigate the in vitro effects of EA on HIV-1 replication, viral enzyme activity and cytokine secretion by infected cells. Methods: The anti-HIV-1 activity of EA in solution was determined in vit...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9695535/ https://www.ncbi.nlm.nih.gov/pubmed/36432041 http://dx.doi.org/10.3390/molecules27227941 |
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author | Nittayananta, Wipawee Promsong, Aornrutai Levy, Claire Hladik, Florian Chaitaveep, Nithinart Ungphaiboon, Suwipa Tewtrakul, Supinya Satthakarn, Surada |
author_facet | Nittayananta, Wipawee Promsong, Aornrutai Levy, Claire Hladik, Florian Chaitaveep, Nithinart Ungphaiboon, Suwipa Tewtrakul, Supinya Satthakarn, Surada |
author_sort | Nittayananta, Wipawee |
collection | PubMed |
description | Objectives: Ellagic acid (EA) has a wide range of biological effects. The purpose of this study was to investigate the in vitro effects of EA on HIV-1 replication, viral enzyme activity and cytokine secretion by infected cells. Methods: The anti-HIV-1 activity of EA in solution was determined in vitro using the infection of TZM-bl cells by the nano luciferase-secreting R5-tropic JRCSF strain of HIV-1, which allows for the quantification of viral growth by measuring nano luciferase in the culture supernatants. The effect of EA on the cytokine secretion of TZM-bl cells was determined by a multiplexed bead array after 48 h of HIV-1 exposure. The antiviral effect of EA in the gel formulation (Ellagel), as would be used for vaginal application, was investigated by the inhibition of infection of UC87.CD4.CCR5 cells with R5-tropic pBaLEnv-recombinant HIV-1. Results: EA in solutions of up to 100 µM was not toxic to TZM-bl cells. EA added either 1 h before or 4 h after HIV-1 exposure suppressed the replication of R5-tropic HIV-1 in TZM-bl cells in a dose-dependent manner, with up to 69% inhibition at 50 µM. EA-containing solutions also exhibited a dose-dependent inhibitory effect on HIV-1 replication in U87 cells. When EA was formulated as a gel, Ellagel containing 25 µM and 50 µM EA inhibited HIV-1 replication in U87 cells by 56% and 84%, respectively. In assays of specific HIV-1 enzyme activity, Ellagel inhibited HIV-1 integrase but not protease. EA did not significantly modulate cytokine secretion. Conclusions: We conclude that EA either in solution or in a gel form inhibits HIV infection without adverse effects on target cells. Thus, gel containing EA can be tested as a new microbicide against HIV infection. |
format | Online Article Text |
id | pubmed-9695535 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-96955352022-11-26 Microbicide Containing Ellagic Acid Can Inhibit HIV-1 Infection Nittayananta, Wipawee Promsong, Aornrutai Levy, Claire Hladik, Florian Chaitaveep, Nithinart Ungphaiboon, Suwipa Tewtrakul, Supinya Satthakarn, Surada Molecules Article Objectives: Ellagic acid (EA) has a wide range of biological effects. The purpose of this study was to investigate the in vitro effects of EA on HIV-1 replication, viral enzyme activity and cytokine secretion by infected cells. Methods: The anti-HIV-1 activity of EA in solution was determined in vitro using the infection of TZM-bl cells by the nano luciferase-secreting R5-tropic JRCSF strain of HIV-1, which allows for the quantification of viral growth by measuring nano luciferase in the culture supernatants. The effect of EA on the cytokine secretion of TZM-bl cells was determined by a multiplexed bead array after 48 h of HIV-1 exposure. The antiviral effect of EA in the gel formulation (Ellagel), as would be used for vaginal application, was investigated by the inhibition of infection of UC87.CD4.CCR5 cells with R5-tropic pBaLEnv-recombinant HIV-1. Results: EA in solutions of up to 100 µM was not toxic to TZM-bl cells. EA added either 1 h before or 4 h after HIV-1 exposure suppressed the replication of R5-tropic HIV-1 in TZM-bl cells in a dose-dependent manner, with up to 69% inhibition at 50 µM. EA-containing solutions also exhibited a dose-dependent inhibitory effect on HIV-1 replication in U87 cells. When EA was formulated as a gel, Ellagel containing 25 µM and 50 µM EA inhibited HIV-1 replication in U87 cells by 56% and 84%, respectively. In assays of specific HIV-1 enzyme activity, Ellagel inhibited HIV-1 integrase but not protease. EA did not significantly modulate cytokine secretion. Conclusions: We conclude that EA either in solution or in a gel form inhibits HIV infection without adverse effects on target cells. Thus, gel containing EA can be tested as a new microbicide against HIV infection. MDPI 2022-11-16 /pmc/articles/PMC9695535/ /pubmed/36432041 http://dx.doi.org/10.3390/molecules27227941 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Nittayananta, Wipawee Promsong, Aornrutai Levy, Claire Hladik, Florian Chaitaveep, Nithinart Ungphaiboon, Suwipa Tewtrakul, Supinya Satthakarn, Surada Microbicide Containing Ellagic Acid Can Inhibit HIV-1 Infection |
title | Microbicide Containing Ellagic Acid Can Inhibit HIV-1 Infection |
title_full | Microbicide Containing Ellagic Acid Can Inhibit HIV-1 Infection |
title_fullStr | Microbicide Containing Ellagic Acid Can Inhibit HIV-1 Infection |
title_full_unstemmed | Microbicide Containing Ellagic Acid Can Inhibit HIV-1 Infection |
title_short | Microbicide Containing Ellagic Acid Can Inhibit HIV-1 Infection |
title_sort | microbicide containing ellagic acid can inhibit hiv-1 infection |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9695535/ https://www.ncbi.nlm.nih.gov/pubmed/36432041 http://dx.doi.org/10.3390/molecules27227941 |
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