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Micronucleus Test of Picrorrhiza Rhizoma Aqueous Extract in Bone Marrow Cells of Male ICR Mice

In this research, the genotoxic effect of Picrorrhiza Rhizoma (PR) aqueous extract was evaluated using the mouse micronucleus test. PR extract was administered once a day for 2 continuous days by oral gavage to male ICR mice at doses of 2000, 1000 and 500 mg/kg. Cyclophosphamide was used as a known...

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Autores principales: Chung, In-Kwon, Cheon, Woo-Hyun, Ku, Sae-Kwang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society of Toxicology 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3834366/
https://www.ncbi.nlm.nih.gov/pubmed/24278560
http://dx.doi.org/10.5487/TR.2011.27.2.119
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author Chung, In-Kwon
Cheon, Woo-Hyun
Ku, Sae-Kwang
author_facet Chung, In-Kwon
Cheon, Woo-Hyun
Ku, Sae-Kwang
author_sort Chung, In-Kwon
collection PubMed
description In this research, the genotoxic effect of Picrorrhiza Rhizoma (PR) aqueous extract was evaluated using the mouse micronucleus test. PR extract was administered once a day for 2 continuous days by oral gavage to male ICR mice at doses of 2000, 1000 and 500 mg/kg. Cyclophosphamide was used as a known genotoxic agent in a positive control. The appearance of a micronucleus (MN) in polychromatic erythrocyte (PCE) is used as an index for genotoxic potential, and PCE ratio is used as an index of cytotoxicity. Although significant (p < 0.01) increase of the number of PCE with one or more nuclei (MNPCE) was detected in cyclophosphamide treated groups, no significant increases of MNPCE numbers were observed in all three different dosages of PR extracts treated mice with over 0.39 of the individual polychromatic erythrocyte ratio in all mice used in this study. The results obtained indicated that PR extract shows no genotoxicity effects up to 2000 mg/kg dosing levels.
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spelling pubmed-38343662013-11-25 Micronucleus Test of Picrorrhiza Rhizoma Aqueous Extract in Bone Marrow Cells of Male ICR Mice Chung, In-Kwon Cheon, Woo-Hyun Ku, Sae-Kwang Toxicol Res Articles In this research, the genotoxic effect of Picrorrhiza Rhizoma (PR) aqueous extract was evaluated using the mouse micronucleus test. PR extract was administered once a day for 2 continuous days by oral gavage to male ICR mice at doses of 2000, 1000 and 500 mg/kg. Cyclophosphamide was used as a known genotoxic agent in a positive control. The appearance of a micronucleus (MN) in polychromatic erythrocyte (PCE) is used as an index for genotoxic potential, and PCE ratio is used as an index of cytotoxicity. Although significant (p < 0.01) increase of the number of PCE with one or more nuclei (MNPCE) was detected in cyclophosphamide treated groups, no significant increases of MNPCE numbers were observed in all three different dosages of PR extracts treated mice with over 0.39 of the individual polychromatic erythrocyte ratio in all mice used in this study. The results obtained indicated that PR extract shows no genotoxicity effects up to 2000 mg/kg dosing levels. The Korean Society of Toxicology 2011-06 /pmc/articles/PMC3834366/ /pubmed/24278560 http://dx.doi.org/10.5487/TR.2011.27.2.119 Text en Copyright ©2011, The Korean Society of Toxicology
spellingShingle Articles
Chung, In-Kwon
Cheon, Woo-Hyun
Ku, Sae-Kwang
Micronucleus Test of Picrorrhiza Rhizoma Aqueous Extract in Bone Marrow Cells of Male ICR Mice
title Micronucleus Test of Picrorrhiza Rhizoma Aqueous Extract in Bone Marrow Cells of Male ICR Mice
title_full Micronucleus Test of Picrorrhiza Rhizoma Aqueous Extract in Bone Marrow Cells of Male ICR Mice
title_fullStr Micronucleus Test of Picrorrhiza Rhizoma Aqueous Extract in Bone Marrow Cells of Male ICR Mice
title_full_unstemmed Micronucleus Test of Picrorrhiza Rhizoma Aqueous Extract in Bone Marrow Cells of Male ICR Mice
title_short Micronucleus Test of Picrorrhiza Rhizoma Aqueous Extract in Bone Marrow Cells of Male ICR Mice
title_sort micronucleus test of picrorrhiza rhizoma aqueous extract in bone marrow cells of male icr mice
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3834366/
https://www.ncbi.nlm.nih.gov/pubmed/24278560
http://dx.doi.org/10.5487/TR.2011.27.2.119
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