The combined effects of BDE47 and BaP on oxidatively generated DNA damage in L02 cells and the possible molecular mechanism

Polybrominated diphenyl ethers (PBDEs) and polycyclic aromatic hydrocarbons (PAHs) coexist widely in the environment and have generated adverse effects on the environment and human health. The purpose of this study was to investigate the combined toxic effects of these chemicals and the related mech...

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Veröffentlicht in:Mutation research 2011-04, Vol.721 (2), p.192-198
Hauptverfasser: An, Jing, Yin, Lingling, Shang, Yu, Zhong, Yufang, Zhang, Xinyu, Wu, Minghong, Yu, Zhiqiang, Sheng, Guoying, Fu, Jiamo, Huang, Yuecheng
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container_issue 2
container_start_page 192
container_title Mutation research
container_volume 721
creator An, Jing
Yin, Lingling
Shang, Yu
Zhong, Yufang
Zhang, Xinyu
Wu, Minghong
Yu, Zhiqiang
Sheng, Guoying
Fu, Jiamo
Huang, Yuecheng
description Polybrominated diphenyl ethers (PBDEs) and polycyclic aromatic hydrocarbons (PAHs) coexist widely in the environment and have generated adverse effects on the environment and human health. The purpose of this study was to investigate the combined toxic effects of these chemicals and the related mechanism. L02 cells were exposed to BDE47 (5, 10 μmol/L) or/and BaP (50 μmol/L) in different administration order. The cell growth and survival, DNA strand breaks, oxidative stress index (ROS, SOD, GSH, and MDA), LDH release and the expression level of CYP1 family members were measured. The result showed that BDE47 or/and BaP had no effect on the cell growth and survival under the present conditions. However, compared with the groups treated with BDE47 or BaP alone, the combined-treated groups induced significantly elevated DNA strand breaks, ROS production, and MDA level. Especially, pretreatment with BDE47 followed by BaP led to the strongest effects. Addition of the antioxidant N-acetyl- l-cysteine (NAC) markedly reduced the ROS level and partly suppressed the DNA strand breaks induced by BDE47 or/and BaP. Meanwhile, the combined treatment groups also markedly increased the SOD activity, GSH content, and LDH release level compared with the control group. The real-time PCR results showed that BaP could significantly induce the expression of CYP1A1 and CYP1B1, however, the pre-treatment with BDE47 appeared to attenuate the BaP-induced CYP1 expression. All of above findings indicated that BDE47 and BaP had a synergistic effect on oxidatively generated DNA damage in L02 cells via regulation on the oxidative stress response and the expression of CYP1 metabolism enzymes.
doi_str_mv 10.1016/j.mrgentox.2011.02.002
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The purpose of this study was to investigate the combined toxic effects of these chemicals and the related mechanism. L02 cells were exposed to BDE47 (5, 10 μmol/L) or/and BaP (50 μmol/L) in different administration order. The cell growth and survival, DNA strand breaks, oxidative stress index (ROS, SOD, GSH, and MDA), LDH release and the expression level of CYP1 family members were measured. The result showed that BDE47 or/and BaP had no effect on the cell growth and survival under the present conditions. However, compared with the groups treated with BDE47 or BaP alone, the combined-treated groups induced significantly elevated DNA strand breaks, ROS production, and MDA level. Especially, pretreatment with BDE47 followed by BaP led to the strongest effects. Addition of the antioxidant N-acetyl- l-cysteine (NAC) markedly reduced the ROS level and partly suppressed the DNA strand breaks induced by BDE47 or/and BaP. Meanwhile, the combined treatment groups also markedly increased the SOD activity, GSH content, and LDH release level compared with the control group. The real-time PCR results showed that BaP could significantly induce the expression of CYP1A1 and CYP1B1, however, the pre-treatment with BDE47 appeared to attenuate the BaP-induced CYP1 expression. All of above findings indicated that BDE47 and BaP had a synergistic effect on oxidatively generated DNA damage in L02 cells via regulation on the oxidative stress response and the expression of CYP1 metabolism enzymes.</abstract><cop>Amsterdam</cop><pub>Elsevier B.V</pub><pmid>21316482</pmid><doi>10.1016/j.mrgentox.2011.02.002</doi><tpages>7</tpages></addata></record>
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subjects Antioxidants
Aryl Hydrocarbon Hydroxylases - metabolism
BaP
BDE47
Benzo(a)pyrene - administration & dosage
Benzo(a)pyrene - toxicity
Biological and medical sciences
Cell growth
Cell Line, Transformed
Cell Proliferation - drug effects
Cell Survival - drug effects
CYP1
Cytochrome P-450 CYP1A1 - metabolism
Cytochrome P-450 CYP1B1
DNA Damage
DNA strand break
Environmental impact
Fundamental and applied biological sciences. Psychology
Genetics of eukaryotes. Biological and molecular evolution
Halogenated Diphenyl Ethers - administration & dosage
Halogenated Diphenyl Ethers - toxicity
Human exposure
Humans
Hydro-Lyases - metabolism
Medical sciences
Metabolism
Mutagens - toxicity
Oxidative stress
Oxidative Stress - drug effects
Polycyclic aromatic hydrocarbons
Toxicity
Toxicology
title The combined effects of BDE47 and BaP on oxidatively generated DNA damage in L02 cells and the possible molecular mechanism
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