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Evaluación del daño oxidativo y por metilación del ADN de pintores expuestos ocupacionalmente a solventes orgánicos y pintura

INTRODUCTION: The exposure to organic solvents and paints has been associated with genotoxicity and a greater risk of neoplasms. However, the type of DNA damage induced in humans by the exposure to these compounds, which would help explain the mechanisms of their genotoxicity, is still not fully cha...

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Autores principales: Londoño-Velasco, Elizabeth, Martínez-Perafán, Fabián, Carvajal, Silvio, García-Vallejo, Felipe, Hoyos-Giraldo, Luz Stella
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Instituto Nacional de Salud 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7357369/
https://www.ncbi.nlm.nih.gov/pubmed/31584761
http://dx.doi.org/10.7705/biomedica.4289
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author Londoño-Velasco, Elizabeth
Martínez-Perafán, Fabián
Carvajal, Silvio
García-Vallejo, Felipe
Hoyos-Giraldo, Luz Stella
author_facet Londoño-Velasco, Elizabeth
Martínez-Perafán, Fabián
Carvajal, Silvio
García-Vallejo, Felipe
Hoyos-Giraldo, Luz Stella
author_sort Londoño-Velasco, Elizabeth
collection PubMed
description INTRODUCTION: The exposure to organic solvents and paints has been associated with genotoxicity and a greater risk of neoplasms. However, the type of DNA damage induced in humans by the exposure to these compounds, which would help explain the mechanisms of their genotoxicity, is still not fully characterized. Due to inadequate practices of occupational safety, car painters in the informal sector are a highly exposed group to organic solvents and paints. OBJECTIVE: To identify the oxidative and methylating damage in the DNA of lymphocytes of car painters exposed to organic solvents and paints. MATERIALS AND METHODS: Isolated peripheral blood lymphocytes from 62 painters and 62 unexposed subjects were analyzed by the modified high-throughput comet assay with the Fpg and AlkA enzymes. The categories used for the evaluation of the DNA damage were basal damage (without enzymes), oxidative and methylating damage. The measurement parameter used to establish the damage was the percentage of DNA in the tail. RESULTS: The percentage of DNA in the tail was higher in the exposed group compared to the unexposed group (p<0.05). In the exposed group, this percentage was higher in the oxidative damage category than the baseline (16.50 vs. 12.87; p<0.001), whereas methylating damage did not show significant differences (14.00 vs. 12.87; p>0.05). CONCLUSION: In this study, exposure to organic solvents and paints was associated with an increase in oxidative lesions in the DNA of car painters’ lymphocytes, such as the production of 8-oxodG and other formamidopyrimidine products which are considered highly mutagenic.
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spelling pubmed-73573692020-07-20 Evaluación del daño oxidativo y por metilación del ADN de pintores expuestos ocupacionalmente a solventes orgánicos y pintura Londoño-Velasco, Elizabeth Martínez-Perafán, Fabián Carvajal, Silvio García-Vallejo, Felipe Hoyos-Giraldo, Luz Stella Biomedica Articulo Original INTRODUCTION: The exposure to organic solvents and paints has been associated with genotoxicity and a greater risk of neoplasms. However, the type of DNA damage induced in humans by the exposure to these compounds, which would help explain the mechanisms of their genotoxicity, is still not fully characterized. Due to inadequate practices of occupational safety, car painters in the informal sector are a highly exposed group to organic solvents and paints. OBJECTIVE: To identify the oxidative and methylating damage in the DNA of lymphocytes of car painters exposed to organic solvents and paints. MATERIALS AND METHODS: Isolated peripheral blood lymphocytes from 62 painters and 62 unexposed subjects were analyzed by the modified high-throughput comet assay with the Fpg and AlkA enzymes. The categories used for the evaluation of the DNA damage were basal damage (without enzymes), oxidative and methylating damage. The measurement parameter used to establish the damage was the percentage of DNA in the tail. RESULTS: The percentage of DNA in the tail was higher in the exposed group compared to the unexposed group (p<0.05). In the exposed group, this percentage was higher in the oxidative damage category than the baseline (16.50 vs. 12.87; p<0.001), whereas methylating damage did not show significant differences (14.00 vs. 12.87; p>0.05). CONCLUSION: In this study, exposure to organic solvents and paints was associated with an increase in oxidative lesions in the DNA of car painters’ lymphocytes, such as the production of 8-oxodG and other formamidopyrimidine products which are considered highly mutagenic. Instituto Nacional de Salud 2019-09-01 /pmc/articles/PMC7357369/ /pubmed/31584761 http://dx.doi.org/10.7705/biomedica.4289 Text en https://creativecommons.org/licenses/by/4.0/ Este es un artículo publicado en acceso abierto bajo una licencia Creative Commons
spellingShingle Articulo Original
Londoño-Velasco, Elizabeth
Martínez-Perafán, Fabián
Carvajal, Silvio
García-Vallejo, Felipe
Hoyos-Giraldo, Luz Stella
Evaluación del daño oxidativo y por metilación del ADN de pintores expuestos ocupacionalmente a solventes orgánicos y pintura
title Evaluación del daño oxidativo y por metilación del ADN de pintores expuestos ocupacionalmente a solventes orgánicos y pintura
title_full Evaluación del daño oxidativo y por metilación del ADN de pintores expuestos ocupacionalmente a solventes orgánicos y pintura
title_fullStr Evaluación del daño oxidativo y por metilación del ADN de pintores expuestos ocupacionalmente a solventes orgánicos y pintura
title_full_unstemmed Evaluación del daño oxidativo y por metilación del ADN de pintores expuestos ocupacionalmente a solventes orgánicos y pintura
title_short Evaluación del daño oxidativo y por metilación del ADN de pintores expuestos ocupacionalmente a solventes orgánicos y pintura
title_sort evaluación del daño oxidativo y por metilación del adn de pintores expuestos ocupacionalmente a solventes orgánicos y pintura
topic Articulo Original
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7357369/
https://www.ncbi.nlm.nih.gov/pubmed/31584761
http://dx.doi.org/10.7705/biomedica.4289
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