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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2018
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.
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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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