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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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Detalles Bibliográficos
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
Descripción
Sumario: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.