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Biotoxicological Analyses of Trimeroside from Baccharis trimera Using a Battery of In Vitro Test Systems
The use in folk medicine of Baccharis trimera and recent studies on DNA damage by oxidative stress mechanisms have motivated this study. We investigated the biotoxicological effects of trimeroside from this plant. Aqueous extract from aerial parts of B. trimera was fractioned by flash chromatography...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6120265/ https://www.ncbi.nlm.nih.gov/pubmed/30210656 http://dx.doi.org/10.1155/2018/7804135 |
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author | dos Santos, Marcela Silva da Silva, Juliana Menezes, Ana Paula Simões de Barros, Francisco Maikon Corrêa Lemes, Maria Luisa Brodt Rossatto, Raíssa R. Feistel, Cleverson de Almeida, Indara Dedigo Grivicich, Ivana Prado, Lismare Picada, Jaqueline Nascimento de Barros Falcão Ferraz, Alexandre |
author_facet | dos Santos, Marcela Silva da Silva, Juliana Menezes, Ana Paula Simões de Barros, Francisco Maikon Corrêa Lemes, Maria Luisa Brodt Rossatto, Raíssa R. Feistel, Cleverson de Almeida, Indara Dedigo Grivicich, Ivana Prado, Lismare Picada, Jaqueline Nascimento de Barros Falcão Ferraz, Alexandre |
author_sort | dos Santos, Marcela Silva |
collection | PubMed |
description | The use in folk medicine of Baccharis trimera and recent studies on DNA damage by oxidative stress mechanisms have motivated this study. We investigated the biotoxicological effects of trimeroside from this plant. Aqueous extract from aerial parts of B. trimera was fractioned by flash chromatography for further isolation by thin-layer chromatography. The novel nor-monoterpene glycoside, trimeroside, and three flavonoids, cirsimaritin, luteolin and quercetin, were isolated. The genotoxic and mutagenic potential of trimeroside was determined by Salmonella/microsome (TA98 and TA100), comet assay, and cytokinesis-block micronucleus cytome assay (CBMN-cyt) in HepG2 cells. We also screened trimeroside into different human tumoral cell lines by sulforhodamine B (SRB) assay. Mutagenicity was detected in TA100 strain with metabolic activation. Genotoxic effects were not observed in HepG2 by comet assay. However, a decrease in the nuclear index division in the 2.0 mg·mL(−1) concentration and an increase of nucleoplasmic bridges in the 1.5 mg·mL(−1) concentration were detected by CBMN-cyt assay indicating cytotoxic and mutagenic effects. In SRB assay, trimeroside showed weak antiproliferative activity against the cell lines. |
format | Online Article Text |
id | pubmed-6120265 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-61202652018-09-12 Biotoxicological Analyses of Trimeroside from Baccharis trimera Using a Battery of In Vitro Test Systems dos Santos, Marcela Silva da Silva, Juliana Menezes, Ana Paula Simões de Barros, Francisco Maikon Corrêa Lemes, Maria Luisa Brodt Rossatto, Raíssa R. Feistel, Cleverson de Almeida, Indara Dedigo Grivicich, Ivana Prado, Lismare Picada, Jaqueline Nascimento de Barros Falcão Ferraz, Alexandre Oxid Med Cell Longev Research Article The use in folk medicine of Baccharis trimera and recent studies on DNA damage by oxidative stress mechanisms have motivated this study. We investigated the biotoxicological effects of trimeroside from this plant. Aqueous extract from aerial parts of B. trimera was fractioned by flash chromatography for further isolation by thin-layer chromatography. The novel nor-monoterpene glycoside, trimeroside, and three flavonoids, cirsimaritin, luteolin and quercetin, were isolated. The genotoxic and mutagenic potential of trimeroside was determined by Salmonella/microsome (TA98 and TA100), comet assay, and cytokinesis-block micronucleus cytome assay (CBMN-cyt) in HepG2 cells. We also screened trimeroside into different human tumoral cell lines by sulforhodamine B (SRB) assay. Mutagenicity was detected in TA100 strain with metabolic activation. Genotoxic effects were not observed in HepG2 by comet assay. However, a decrease in the nuclear index division in the 2.0 mg·mL(−1) concentration and an increase of nucleoplasmic bridges in the 1.5 mg·mL(−1) concentration were detected by CBMN-cyt assay indicating cytotoxic and mutagenic effects. In SRB assay, trimeroside showed weak antiproliferative activity against the cell lines. Hindawi 2018-08-19 /pmc/articles/PMC6120265/ /pubmed/30210656 http://dx.doi.org/10.1155/2018/7804135 Text en Copyright © 2018 Marcela Silva dos Santos et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article dos Santos, Marcela Silva da Silva, Juliana Menezes, Ana Paula Simões de Barros, Francisco Maikon Corrêa Lemes, Maria Luisa Brodt Rossatto, Raíssa R. Feistel, Cleverson de Almeida, Indara Dedigo Grivicich, Ivana Prado, Lismare Picada, Jaqueline Nascimento de Barros Falcão Ferraz, Alexandre Biotoxicological Analyses of Trimeroside from Baccharis trimera Using a Battery of In Vitro Test Systems |
title | Biotoxicological Analyses of Trimeroside from Baccharis trimera Using a Battery of In Vitro Test Systems |
title_full | Biotoxicological Analyses of Trimeroside from Baccharis trimera Using a Battery of In Vitro Test Systems |
title_fullStr | Biotoxicological Analyses of Trimeroside from Baccharis trimera Using a Battery of In Vitro Test Systems |
title_full_unstemmed | Biotoxicological Analyses of Trimeroside from Baccharis trimera Using a Battery of In Vitro Test Systems |
title_short | Biotoxicological Analyses of Trimeroside from Baccharis trimera Using a Battery of In Vitro Test Systems |
title_sort | biotoxicological analyses of trimeroside from baccharis trimera using a battery of in vitro test systems |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6120265/ https://www.ncbi.nlm.nih.gov/pubmed/30210656 http://dx.doi.org/10.1155/2018/7804135 |
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