Synergistic in vitro interactions between (22S,23S)-3β-bromo-5α, 22,23-trihydroxystigmastan-6-one and acyclovir or foscarnet against herpes simplex virus type 1
The replication of herpes simplex virus (HSV) type 1 in Vero cells is inhibited in the presence of (22S,23S)-3β-bromo-5α,22,23- trihydroxystigmastan-6-one (6b), a synthetic brassinosteroid derivative. Since a late step of virus multiplication is hindered by 6b, we performed studies of drug-drug comb...
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Acceso en línea: | https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00093157_v52_n1_p38_Talarico http://hdl.handle.net/20.500.12110/paper_00093157_v52_n1_p38_Talarico |
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paper:paper_00093157_v52_n1_p38_Talarico2023-06-08T14:34:00Z Synergistic in vitro interactions between (22S,23S)-3β-bromo-5α, 22,23-trihydroxystigmastan-6-one and acyclovir or foscarnet against herpes simplex virus type 1 Talarico, Laura Beatriz Castilla, Viviana Ramirez, Javier Alberto Wachsman, Mónica Beatriz (22S,23S)-3β-bromo- 5α,22,23-trihydroxystigmastan-6-one Antiviral drug-drug combinations Brassinosteroid derivatives Herpes simplex 3beta bromo 5alpha,22,23 trihydroxystigmastan 6 one aciclovir antivirus agent foscarnet unclassified drug antiviral activity article controlled study DNA sequence drug activity drug potentiation gene frequency gene mutation gene targeting Herpes simplex virus nonhuman priority journal protein phosphorylation virogenesis Acyclovir Animals Antiviral Agents Cell Line Cell Proliferation Cercopithecus aethiops Cholestanones Drug Synergism Foscarnet Herpesvirus 1, Human Molecular Structure The replication of herpes simplex virus (HSV) type 1 in Vero cells is inhibited in the presence of (22S,23S)-3β-bromo-5α,22,23- trihydroxystigmastan-6-one (6b), a synthetic brassinosteroid derivative. Since a late step of virus multiplication is hindered by 6b, we performed studies of drug-drug combination with acyclovir (ACV) and foscarnet (FOS). It was determined that 6b would act synergistically with low concentrations of ACV and moderate concentrations of FOS against HSV. The best drug combination tested in this study resulted in an increase of 29.3 and 47.2% in antiviral activity for ACV (0.036 μM) and FOS (37.5 μM) in the presence of 14.8 and 6.9 μM of 6b, respectively. Copyright © 2006 S. Karger AG. Fil:Talarico, L.B. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Castilla, V. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Ramirez, J.A. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Wachsman, M.B. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. 2005 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00093157_v52_n1_p38_Talarico http://hdl.handle.net/20.500.12110/paper_00093157_v52_n1_p38_Talarico |
institution |
Universidad de Buenos Aires |
institution_str |
I-28 |
repository_str |
R-134 |
collection |
Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA) |
topic |
(22S,23S)-3β-bromo- 5α,22,23-trihydroxystigmastan-6-one Antiviral drug-drug combinations Brassinosteroid derivatives Herpes simplex 3beta bromo 5alpha,22,23 trihydroxystigmastan 6 one aciclovir antivirus agent foscarnet unclassified drug antiviral activity article controlled study DNA sequence drug activity drug potentiation gene frequency gene mutation gene targeting Herpes simplex virus nonhuman priority journal protein phosphorylation virogenesis Acyclovir Animals Antiviral Agents Cell Line Cell Proliferation Cercopithecus aethiops Cholestanones Drug Synergism Foscarnet Herpesvirus 1, Human Molecular Structure |
spellingShingle |
(22S,23S)-3β-bromo- 5α,22,23-trihydroxystigmastan-6-one Antiviral drug-drug combinations Brassinosteroid derivatives Herpes simplex 3beta bromo 5alpha,22,23 trihydroxystigmastan 6 one aciclovir antivirus agent foscarnet unclassified drug antiviral activity article controlled study DNA sequence drug activity drug potentiation gene frequency gene mutation gene targeting Herpes simplex virus nonhuman priority journal protein phosphorylation virogenesis Acyclovir Animals Antiviral Agents Cell Line Cell Proliferation Cercopithecus aethiops Cholestanones Drug Synergism Foscarnet Herpesvirus 1, Human Molecular Structure Talarico, Laura Beatriz Castilla, Viviana Ramirez, Javier Alberto Wachsman, Mónica Beatriz Synergistic in vitro interactions between (22S,23S)-3β-bromo-5α, 22,23-trihydroxystigmastan-6-one and acyclovir or foscarnet against herpes simplex virus type 1 |
topic_facet |
(22S,23S)-3β-bromo- 5α,22,23-trihydroxystigmastan-6-one Antiviral drug-drug combinations Brassinosteroid derivatives Herpes simplex 3beta bromo 5alpha,22,23 trihydroxystigmastan 6 one aciclovir antivirus agent foscarnet unclassified drug antiviral activity article controlled study DNA sequence drug activity drug potentiation gene frequency gene mutation gene targeting Herpes simplex virus nonhuman priority journal protein phosphorylation virogenesis Acyclovir Animals Antiviral Agents Cell Line Cell Proliferation Cercopithecus aethiops Cholestanones Drug Synergism Foscarnet Herpesvirus 1, Human Molecular Structure |
description |
The replication of herpes simplex virus (HSV) type 1 in Vero cells is inhibited in the presence of (22S,23S)-3β-bromo-5α,22,23- trihydroxystigmastan-6-one (6b), a synthetic brassinosteroid derivative. Since a late step of virus multiplication is hindered by 6b, we performed studies of drug-drug combination with acyclovir (ACV) and foscarnet (FOS). It was determined that 6b would act synergistically with low concentrations of ACV and moderate concentrations of FOS against HSV. The best drug combination tested in this study resulted in an increase of 29.3 and 47.2% in antiviral activity for ACV (0.036 μM) and FOS (37.5 μM) in the presence of 14.8 and 6.9 μM of 6b, respectively. Copyright © 2006 S. Karger AG. |
author |
Talarico, Laura Beatriz Castilla, Viviana Ramirez, Javier Alberto Wachsman, Mónica Beatriz |
author_facet |
Talarico, Laura Beatriz Castilla, Viviana Ramirez, Javier Alberto Wachsman, Mónica Beatriz |
author_sort |
Talarico, Laura Beatriz |
title |
Synergistic in vitro interactions between (22S,23S)-3β-bromo-5α, 22,23-trihydroxystigmastan-6-one and acyclovir or foscarnet against herpes simplex virus type 1 |
title_short |
Synergistic in vitro interactions between (22S,23S)-3β-bromo-5α, 22,23-trihydroxystigmastan-6-one and acyclovir or foscarnet against herpes simplex virus type 1 |
title_full |
Synergistic in vitro interactions between (22S,23S)-3β-bromo-5α, 22,23-trihydroxystigmastan-6-one and acyclovir or foscarnet against herpes simplex virus type 1 |
title_fullStr |
Synergistic in vitro interactions between (22S,23S)-3β-bromo-5α, 22,23-trihydroxystigmastan-6-one and acyclovir or foscarnet against herpes simplex virus type 1 |
title_full_unstemmed |
Synergistic in vitro interactions between (22S,23S)-3β-bromo-5α, 22,23-trihydroxystigmastan-6-one and acyclovir or foscarnet against herpes simplex virus type 1 |
title_sort |
synergistic in vitro interactions between (22s,23s)-3β-bromo-5α, 22,23-trihydroxystigmastan-6-one and acyclovir or foscarnet against herpes simplex virus type 1 |
publishDate |
2005 |
url |
https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00093157_v52_n1_p38_Talarico http://hdl.handle.net/20.500.12110/paper_00093157_v52_n1_p38_Talarico |
work_keys_str_mv |
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