Lack of clastogenic effects of L-thyroxine in whole-blood cultured human lymphocytes
Thyroid hormones stimulate aerobic metabolism which may lead to oxidative stress accompanied by damage to various cellular macromolecules, including DNA. Previous comet assay studies have shown that thyroid hormones cause DNA damage due to the creation of reactive oxygen species (ROS). However, cyto...
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Format: | Article |
Language: | English |
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Sociedade Brasileira de Genética
2007-01-01
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Series: | Genetics and Molecular Biology |
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Online Access: | http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572007000600019 |
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author | Ninoslav Djelic Dijana Djelic Biljana Spremo-Potparevic Lada Zivkovic Biljana Markovic Olivera Lozance Milos Blagojevic |
author_facet | Ninoslav Djelic Dijana Djelic Biljana Spremo-Potparevic Lada Zivkovic Biljana Markovic Olivera Lozance Milos Blagojevic |
author_sort | Ninoslav Djelic |
collection | DOAJ |
description | Thyroid hormones stimulate aerobic metabolism which may lead to oxidative stress accompanied by damage to various cellular macromolecules, including DNA. Previous comet assay studies have shown that thyroid hormones cause DNA damage due to the creation of reactive oxygen species (ROS). However, cytogenetic studies have been equivocal because although an increase in the sister-chromatid exchange frequency per cell has been reported increased micronuclei frequency has not. We used cytogenetic examination of chromosome breakage and aberrations in whole-blood cultures of human peripheral blood lymphocytes to investigate possible clastogenic effects when lymphocytes were exposed to 0.002 µM to 50 µM of L-thyroxine for 24 h and 48 h, these concentrations being chosen because they had been used in previous studies of sister-chromatid exchange and micronuclei frequency. Under our experimental conditions thyroxine did not induced any statistically significant increase in chromosome breakage or aberrations. This lack of clastogenic effects is in contrast to the reported comet assay results obtained using purified lymphocytes, possibly because whole-blood cultures contain catalase and glutathione peroxidase capable of reducing the effects of reactive oxygen species. |
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issn | 1415-4757 1678-4685 |
language | English |
last_indexed | 2024-04-12T11:43:07Z |
publishDate | 2007-01-01 |
publisher | Sociedade Brasileira de Genética |
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series | Genetics and Molecular Biology |
spelling | doaj.art-b197de014f66490284a45d2273f521e82022-12-22T03:34:33ZengSociedade Brasileira de GenéticaGenetics and Molecular Biology1415-47571678-46852007-01-013041144114910.1590/S1415-47572007000600019Lack of clastogenic effects of L-thyroxine in whole-blood cultured human lymphocytesNinoslav DjelicDijana DjelicBiljana Spremo-PotparevicLada ZivkovicBiljana MarkovicOlivera LozanceMilos BlagojevicThyroid hormones stimulate aerobic metabolism which may lead to oxidative stress accompanied by damage to various cellular macromolecules, including DNA. Previous comet assay studies have shown that thyroid hormones cause DNA damage due to the creation of reactive oxygen species (ROS). However, cytogenetic studies have been equivocal because although an increase in the sister-chromatid exchange frequency per cell has been reported increased micronuclei frequency has not. We used cytogenetic examination of chromosome breakage and aberrations in whole-blood cultures of human peripheral blood lymphocytes to investigate possible clastogenic effects when lymphocytes were exposed to 0.002 µM to 50 µM of L-thyroxine for 24 h and 48 h, these concentrations being chosen because they had been used in previous studies of sister-chromatid exchange and micronuclei frequency. Under our experimental conditions thyroxine did not induced any statistically significant increase in chromosome breakage or aberrations. This lack of clastogenic effects is in contrast to the reported comet assay results obtained using purified lymphocytes, possibly because whole-blood cultures contain catalase and glutathione peroxidase capable of reducing the effects of reactive oxygen species.http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572007000600019thyroxinehuman lymphocyteschromosome aberrationsmitotic indexROS |
spellingShingle | Ninoslav Djelic Dijana Djelic Biljana Spremo-Potparevic Lada Zivkovic Biljana Markovic Olivera Lozance Milos Blagojevic Lack of clastogenic effects of L-thyroxine in whole-blood cultured human lymphocytes Genetics and Molecular Biology thyroxine human lymphocytes chromosome aberrations mitotic index ROS |
title | Lack of clastogenic effects of L-thyroxine in whole-blood cultured human lymphocytes |
title_full | Lack of clastogenic effects of L-thyroxine in whole-blood cultured human lymphocytes |
title_fullStr | Lack of clastogenic effects of L-thyroxine in whole-blood cultured human lymphocytes |
title_full_unstemmed | Lack of clastogenic effects of L-thyroxine in whole-blood cultured human lymphocytes |
title_short | Lack of clastogenic effects of L-thyroxine in whole-blood cultured human lymphocytes |
title_sort | lack of clastogenic effects of l thyroxine in whole blood cultured human lymphocytes |
topic | thyroxine human lymphocytes chromosome aberrations mitotic index ROS |
url | http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572007000600019 |
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