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Vitamin B12 protects against DNA damage induced by hydrochlorothiazide
DNA damage induced by hydrochlorothiazide was previously reported in cultured human lymphocytes. In this study, we aimed to investigate the harmful effects of hydrochlorothiazide on DNA by measuring the spontaneous frequency of sister chromatid exchanges (SCEs) in cultured human lymphocytes. We also...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6128724/ https://www.ncbi.nlm.nih.gov/pubmed/30202218 http://dx.doi.org/10.1016/j.jsps.2018.04.005 |
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author | Alzoubi, Karem H. Bayraktar, Erva Khabour, Omar Al-Azzam, Sayer I. |
author_facet | Alzoubi, Karem H. Bayraktar, Erva Khabour, Omar Al-Azzam, Sayer I. |
author_sort | Alzoubi, Karem H. |
collection | PubMed |
description | DNA damage induced by hydrochlorothiazide was previously reported in cultured human lymphocytes. In this study, we aimed to investigate the harmful effects of hydrochlorothiazide on DNA by measuring the spontaneous frequency of sister chromatid exchanges (SCEs) in cultured human lymphocytes. We also aimed to investigate the possible protection of that damage by vitamin B12. The results showed that hydrochlorothiazide (5 µg/mL) significantly increased the frequency of sister chromatid exchanges (P < 0.001) in human lymphocytes in comparison with control. Additionally, the frequency of hydrochlorothiazide-induced SCEs was significantly decreased by co-treatment with vitamin B12 at concentration of 13.5 µg/mL (P < 0.001). In conclusion, hydrochlorothiazide is genotoxic to human lymphocytes and its toxicity is reduced by vitamin B12. |
format | Online Article Text |
id | pubmed-6128724 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-61287242018-09-10 Vitamin B12 protects against DNA damage induced by hydrochlorothiazide Alzoubi, Karem H. Bayraktar, Erva Khabour, Omar Al-Azzam, Sayer I. Saudi Pharm J Article DNA damage induced by hydrochlorothiazide was previously reported in cultured human lymphocytes. In this study, we aimed to investigate the harmful effects of hydrochlorothiazide on DNA by measuring the spontaneous frequency of sister chromatid exchanges (SCEs) in cultured human lymphocytes. We also aimed to investigate the possible protection of that damage by vitamin B12. The results showed that hydrochlorothiazide (5 µg/mL) significantly increased the frequency of sister chromatid exchanges (P < 0.001) in human lymphocytes in comparison with control. Additionally, the frequency of hydrochlorothiazide-induced SCEs was significantly decreased by co-treatment with vitamin B12 at concentration of 13.5 µg/mL (P < 0.001). In conclusion, hydrochlorothiazide is genotoxic to human lymphocytes and its toxicity is reduced by vitamin B12. Elsevier 2018-09 2018-04-03 /pmc/articles/PMC6128724/ /pubmed/30202218 http://dx.doi.org/10.1016/j.jsps.2018.04.005 Text en © 2018 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Alzoubi, Karem H. Bayraktar, Erva Khabour, Omar Al-Azzam, Sayer I. Vitamin B12 protects against DNA damage induced by hydrochlorothiazide |
title | Vitamin B12 protects against DNA damage induced by hydrochlorothiazide |
title_full | Vitamin B12 protects against DNA damage induced by hydrochlorothiazide |
title_fullStr | Vitamin B12 protects against DNA damage induced by hydrochlorothiazide |
title_full_unstemmed | Vitamin B12 protects against DNA damage induced by hydrochlorothiazide |
title_short | Vitamin B12 protects against DNA damage induced by hydrochlorothiazide |
title_sort | vitamin b12 protects against dna damage induced by hydrochlorothiazide |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6128724/ https://www.ncbi.nlm.nih.gov/pubmed/30202218 http://dx.doi.org/10.1016/j.jsps.2018.04.005 |
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