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Antimutagenicity of Methanolic Extracts from Anemopsis californica in Relation to Their Antioxidant Activity

Anemopsis californica has been used empirically to treat infectious diseases. However, there are no antimutagenic evaluation reports on this plant. The present study evaluated the antioxidant activity in relation to the mutagenic and antimutagenic activity properties of leaf (LME) and stem (SME) met...

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Autores principales: Del-Toro-Sánchez, Carmen Lizette, Bautista-Bautista, Nereyda, Blasco-Cabal, José Luis, Gonzalez-Ávila, Marisela, Gutiérrez-Lomelí, Melesio, Arriaga-Alba, Myriam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4135139/
https://www.ncbi.nlm.nih.gov/pubmed/25152760
http://dx.doi.org/10.1155/2014/273878
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author Del-Toro-Sánchez, Carmen Lizette
Bautista-Bautista, Nereyda
Blasco-Cabal, José Luis
Gonzalez-Ávila, Marisela
Gutiérrez-Lomelí, Melesio
Arriaga-Alba, Myriam
author_facet Del-Toro-Sánchez, Carmen Lizette
Bautista-Bautista, Nereyda
Blasco-Cabal, José Luis
Gonzalez-Ávila, Marisela
Gutiérrez-Lomelí, Melesio
Arriaga-Alba, Myriam
author_sort Del-Toro-Sánchez, Carmen Lizette
collection PubMed
description Anemopsis californica has been used empirically to treat infectious diseases. However, there are no antimutagenic evaluation reports on this plant. The present study evaluated the antioxidant activity in relation to the mutagenic and antimutagenic activity properties of leaf (LME) and stem (SME) methanolic extracts of A. californica collected in the central Mexican state of Querétaro. Antioxidant properties and total phenols of extracts were evaluated using DPPH (1,1-diphenyl-2-picrylhydrazyl) and Folin-Ciocalteu methods, respectively. Mutagenicity was evaluated using the Ames test employing Salmonella enterica serovar Typhimurium strains (TA98, TA100, and TA102), with and without an aroclor 1254 (S9 mixture). Antimutagenesis was performed against mutations induced on the Ames test with MNNG, 2AA, or 4NQO. SME presented the highest antioxidant capacity and total phenolic content. None of the extracts exhibited mutagenicity in the Ames test. The extracts produced a significant reduction in 2AA-induced mutations in S. typhimurium TA98. In both extracts, mutagenesis induced by 4NQO or methyl-N′-nitro-N-nitrosoguanidine (MNNG) was reduced only if the exposure of strains was <10 μg/Petri dish. A. californca antioxidant properties and its capacity to reduce point mutations render it suitable to enhance medical cancer treatments. The significant effect against antimutagenic 2AA suggests that their consumption would provide protection against carcinogenic polycyclic aromatic compounds.
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spelling pubmed-41351392014-08-24 Antimutagenicity of Methanolic Extracts from Anemopsis californica in Relation to Their Antioxidant Activity Del-Toro-Sánchez, Carmen Lizette Bautista-Bautista, Nereyda Blasco-Cabal, José Luis Gonzalez-Ávila, Marisela Gutiérrez-Lomelí, Melesio Arriaga-Alba, Myriam Evid Based Complement Alternat Med Research Article Anemopsis californica has been used empirically to treat infectious diseases. However, there are no antimutagenic evaluation reports on this plant. The present study evaluated the antioxidant activity in relation to the mutagenic and antimutagenic activity properties of leaf (LME) and stem (SME) methanolic extracts of A. californica collected in the central Mexican state of Querétaro. Antioxidant properties and total phenols of extracts were evaluated using DPPH (1,1-diphenyl-2-picrylhydrazyl) and Folin-Ciocalteu methods, respectively. Mutagenicity was evaluated using the Ames test employing Salmonella enterica serovar Typhimurium strains (TA98, TA100, and TA102), with and without an aroclor 1254 (S9 mixture). Antimutagenesis was performed against mutations induced on the Ames test with MNNG, 2AA, or 4NQO. SME presented the highest antioxidant capacity and total phenolic content. None of the extracts exhibited mutagenicity in the Ames test. The extracts produced a significant reduction in 2AA-induced mutations in S. typhimurium TA98. In both extracts, mutagenesis induced by 4NQO or methyl-N′-nitro-N-nitrosoguanidine (MNNG) was reduced only if the exposure of strains was <10 μg/Petri dish. A. californca antioxidant properties and its capacity to reduce point mutations render it suitable to enhance medical cancer treatments. The significant effect against antimutagenic 2AA suggests that their consumption would provide protection against carcinogenic polycyclic aromatic compounds. Hindawi Publishing Corporation 2014 2014-07-23 /pmc/articles/PMC4135139/ /pubmed/25152760 http://dx.doi.org/10.1155/2014/273878 Text en Copyright © 2014 Carmen Lizette Del-Toro-Sánchez et al. https://creativecommons.org/licenses/by/3.0/ 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
Del-Toro-Sánchez, Carmen Lizette
Bautista-Bautista, Nereyda
Blasco-Cabal, José Luis
Gonzalez-Ávila, Marisela
Gutiérrez-Lomelí, Melesio
Arriaga-Alba, Myriam
Antimutagenicity of Methanolic Extracts from Anemopsis californica in Relation to Their Antioxidant Activity
title Antimutagenicity of Methanolic Extracts from Anemopsis californica in Relation to Their Antioxidant Activity
title_full Antimutagenicity of Methanolic Extracts from Anemopsis californica in Relation to Their Antioxidant Activity
title_fullStr Antimutagenicity of Methanolic Extracts from Anemopsis californica in Relation to Their Antioxidant Activity
title_full_unstemmed Antimutagenicity of Methanolic Extracts from Anemopsis californica in Relation to Their Antioxidant Activity
title_short Antimutagenicity of Methanolic Extracts from Anemopsis californica in Relation to Their Antioxidant Activity
title_sort antimutagenicity of methanolic extracts from anemopsis californica in relation to their antioxidant activity
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4135139/
https://www.ncbi.nlm.nih.gov/pubmed/25152760
http://dx.doi.org/10.1155/2014/273878
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