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Analysis of the Interactions of Botanical Extract Combinations Against the Viability of Prostate Cancer Cell Lines

Herbal medicines are often combinations of botanical extracts that are assumed to have additive or synergistic effects. The purpose of this investigation was to compare the effect of individual botanical extracts with combinations of extracts on prostate cell viability. We then modeled the interacti...

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Detalles Bibliográficos
Autores principales: Adams, Lynn S., Seeram, Navindra P., Hardy, Mary L., Carpenter, Catherine, Heber, David
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1375246/
https://www.ncbi.nlm.nih.gov/pubmed/16550232
http://dx.doi.org/10.1093/ecam/nel001
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author Adams, Lynn S.
Seeram, Navindra P.
Hardy, Mary L.
Carpenter, Catherine
Heber, David
author_facet Adams, Lynn S.
Seeram, Navindra P.
Hardy, Mary L.
Carpenter, Catherine
Heber, David
author_sort Adams, Lynn S.
collection PubMed
description Herbal medicines are often combinations of botanical extracts that are assumed to have additive or synergistic effects. The purpose of this investigation was to compare the effect of individual botanical extracts with combinations of extracts on prostate cell viability. We then modeled the interactions between botanical extracts in combination isobolographically. Scutellaria baicalensis, Rabdosia rubescens, Panax-pseudo ginseng, Dendranthema morifolium, Glycyrrhiza uralensis and Serenoa repens were collected, taxonomically identified and extracts prepared. Effects of the extracts on cell viability were quantitated in prostate cell lines using a luminescent ATP cell viability assay. Combinations of two botanical extracts of the four most active extracts were tested in the 22Rv1 cell line and their interactions assessed using isobolographic analysis. Each extract significantly inhibited the proliferation of prostate cell lines in a time- and dose-dependent manner except S. repens. The most active extracts, S. baicalensis, D. morifolium, G. uralensis and R. rubescens were tested as two-extract combinations. S. baicalensis and D. morifolium when combined were additive with a trend toward synergy, whereas D. morifolium and R. rubescens together were additive. The remaining two-extract combinations showed antagonism. The four extracts together were significantly more effective than the two-by-two combinations and the individual extracts alone. Combining the four herbal extracts significantly enhanced their activity in the cell lines tested compared with extracts alone. The less predictable nature of the two-way combinations suggests a need for careful characterization of the effects of each individual herb based on their intended use.
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spelling pubmed-13752462006-03-20 Analysis of the Interactions of Botanical Extract Combinations Against the Viability of Prostate Cancer Cell Lines Adams, Lynn S. Seeram, Navindra P. Hardy, Mary L. Carpenter, Catherine Heber, David Evid Based Complement Alternat Med Original Articles Herbal medicines are often combinations of botanical extracts that are assumed to have additive or synergistic effects. The purpose of this investigation was to compare the effect of individual botanical extracts with combinations of extracts on prostate cell viability. We then modeled the interactions between botanical extracts in combination isobolographically. Scutellaria baicalensis, Rabdosia rubescens, Panax-pseudo ginseng, Dendranthema morifolium, Glycyrrhiza uralensis and Serenoa repens were collected, taxonomically identified and extracts prepared. Effects of the extracts on cell viability were quantitated in prostate cell lines using a luminescent ATP cell viability assay. Combinations of two botanical extracts of the four most active extracts were tested in the 22Rv1 cell line and their interactions assessed using isobolographic analysis. Each extract significantly inhibited the proliferation of prostate cell lines in a time- and dose-dependent manner except S. repens. The most active extracts, S. baicalensis, D. morifolium, G. uralensis and R. rubescens were tested as two-extract combinations. S. baicalensis and D. morifolium when combined were additive with a trend toward synergy, whereas D. morifolium and R. rubescens together were additive. The remaining two-extract combinations showed antagonism. The four extracts together were significantly more effective than the two-by-two combinations and the individual extracts alone. Combining the four herbal extracts significantly enhanced their activity in the cell lines tested compared with extracts alone. The less predictable nature of the two-way combinations suggests a need for careful characterization of the effects of each individual herb based on their intended use. Oxford University Press 2006-03 /pmc/articles/PMC1375246/ /pubmed/16550232 http://dx.doi.org/10.1093/ecam/nel001 Text en © The Author (2006). Published by Oxford University Press. All rights reserved
spellingShingle Original Articles
Adams, Lynn S.
Seeram, Navindra P.
Hardy, Mary L.
Carpenter, Catherine
Heber, David
Analysis of the Interactions of Botanical Extract Combinations Against the Viability of Prostate Cancer Cell Lines
title Analysis of the Interactions of Botanical Extract Combinations Against the Viability of Prostate Cancer Cell Lines
title_full Analysis of the Interactions of Botanical Extract Combinations Against the Viability of Prostate Cancer Cell Lines
title_fullStr Analysis of the Interactions of Botanical Extract Combinations Against the Viability of Prostate Cancer Cell Lines
title_full_unstemmed Analysis of the Interactions of Botanical Extract Combinations Against the Viability of Prostate Cancer Cell Lines
title_short Analysis of the Interactions of Botanical Extract Combinations Against the Viability of Prostate Cancer Cell Lines
title_sort analysis of the interactions of botanical extract combinations against the viability of prostate cancer cell lines
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1375246/
https://www.ncbi.nlm.nih.gov/pubmed/16550232
http://dx.doi.org/10.1093/ecam/nel001
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