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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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 |
format | Article |
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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.</description><identifier>ISSN: 1383-5718</identifier><identifier>ISSN: 0027-5107</identifier><identifier>EISSN: 1879-3592</identifier><identifier>DOI: 10.1016/j.mrgentox.2011.02.002</identifier><identifier>PMID: 21316482</identifier><language>eng</language><publisher>Amsterdam: Elsevier B.V</publisher><subject>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</subject><ispartof>Mutation research, 2011-04, Vol.721 (2), p.192-198</ispartof><rights>2011 Elsevier B.V.</rights><rights>2015 INIST-CNRS</rights><rights>Copyright © 2011 Elsevier B.V. All rights reserved.</rights><rights>Copyright Elsevier BV Apr 3, 2011</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c522t-99edf6ad36401975cd64b4ea3345f72465b2a94714c6d840d2edf8b588fb99813</citedby><cites>FETCH-LOGICAL-c522t-99edf6ad36401975cd64b4ea3345f72465b2a94714c6d840d2edf8b588fb99813</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S138357181100043X$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65534</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=24084668$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21316482$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>An, Jing</creatorcontrib><creatorcontrib>Yin, Lingling</creatorcontrib><creatorcontrib>Shang, Yu</creatorcontrib><creatorcontrib>Zhong, Yufang</creatorcontrib><creatorcontrib>Zhang, Xinyu</creatorcontrib><creatorcontrib>Wu, Minghong</creatorcontrib><creatorcontrib>Yu, Zhiqiang</creatorcontrib><creatorcontrib>Sheng, Guoying</creatorcontrib><creatorcontrib>Fu, Jiamo</creatorcontrib><creatorcontrib>Huang, Yuecheng</creatorcontrib><title>The combined effects of BDE47 and BaP on oxidatively generated DNA damage in L02 cells and the possible molecular mechanism</title><title>Mutation research</title><addtitle>Mutat Res</addtitle><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.</description><subject>Antioxidants</subject><subject>Aryl Hydrocarbon Hydroxylases - metabolism</subject><subject>BaP</subject><subject>BDE47</subject><subject>Benzo(a)pyrene - administration & dosage</subject><subject>Benzo(a)pyrene - toxicity</subject><subject>Biological and medical sciences</subject><subject>Cell growth</subject><subject>Cell Line, Transformed</subject><subject>Cell Proliferation - drug effects</subject><subject>Cell Survival - drug effects</subject><subject>CYP1</subject><subject>Cytochrome P-450 CYP1A1 - metabolism</subject><subject>Cytochrome P-450 CYP1B1</subject><subject>DNA Damage</subject><subject>DNA strand break</subject><subject>Environmental impact</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Genetics of eukaryotes. Biological and molecular evolution</subject><subject>Halogenated Diphenyl Ethers - administration & dosage</subject><subject>Halogenated Diphenyl Ethers - toxicity</subject><subject>Human exposure</subject><subject>Humans</subject><subject>Hydro-Lyases - metabolism</subject><subject>Medical sciences</subject><subject>Metabolism</subject><subject>Mutagens - toxicity</subject><subject>Oxidative stress</subject><subject>Oxidative Stress - drug effects</subject><subject>Polycyclic aromatic hydrocarbons</subject><subject>Toxicity</subject><subject>Toxicology</subject><issn>1383-5718</issn><issn>0027-5107</issn><issn>1879-3592</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkUtv1DAUhS0EakvpX6isSohVgl9xnF2fPKQRsChry7FvWo8Se7CTqhV_Hg8zBYkNK3vxnXPPvQehU0pqSqh8v66ndAdhjo81I5TWhNWEsBfoiKq2q3jTsZflzxWvmpaqQ_Q653UBCCfqAB0yyqkUih2hn7f3gG2ceh_AYRgGsHPGccCX1zeixSY4fGm-4RhwfPTOzP4BxidcJkMyc1Fcf7nAzkzmDrAPeEUYtjCO-bdwLtabmLPvR8BTHMEuo0l4Antvgs_TG_RqMGOGk_17jL5_uLm9-lStvn78fHWxqmzD2Fx1HbhBGselILRrG-uk6AUYzkUztEzIpmemEy0VVjoliGOFV32j1NB3naL8GL3b-W5S_LFAnvXk8zamCRCXrJVsW8Eaygp59g-5jksKJVyByiTVtVs7uYNsKsslGPQm-cmkJ02J3paj1_q5HL0tRxOmy-2L8HTvvvQTuD-y5zYK8HYPmGzNOCQTrM9_OUGUkFIV7nzHQbnag4eks_UQLDifSn_aRf-_LL8Aa4WvHw</recordid><startdate>20110403</startdate><enddate>20110403</enddate><creator>An, Jing</creator><creator>Yin, Lingling</creator><creator>Shang, Yu</creator><creator>Zhong, Yufang</creator><creator>Zhang, Xinyu</creator><creator>Wu, Minghong</creator><creator>Yu, Zhiqiang</creator><creator>Sheng, Guoying</creator><creator>Fu, Jiamo</creator><creator>Huang, Yuecheng</creator><general>Elsevier B.V</general><general>Elsevier</general><general>Elsevier BV</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7ST</scope><scope>7TM</scope><scope>7U7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope><scope>SOI</scope><scope>7TV</scope></search><sort><creationdate>20110403</creationdate><title>The combined effects of BDE47 and BaP on oxidatively generated DNA damage in L02 cells and the possible molecular mechanism</title><author>An, Jing ; Yin, Lingling ; Shang, Yu ; Zhong, Yufang ; Zhang, Xinyu ; Wu, Minghong ; Yu, Zhiqiang ; Sheng, Guoying ; Fu, Jiamo ; Huang, Yuecheng</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c522t-99edf6ad36401975cd64b4ea3345f72465b2a94714c6d840d2edf8b588fb99813</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Antioxidants</topic><topic>Aryl Hydrocarbon Hydroxylases - metabolism</topic><topic>BaP</topic><topic>BDE47</topic><topic>Benzo(a)pyrene - administration & dosage</topic><topic>Benzo(a)pyrene - toxicity</topic><topic>Biological and medical sciences</topic><topic>Cell growth</topic><topic>Cell Line, Transformed</topic><topic>Cell Proliferation - drug effects</topic><topic>Cell Survival - drug effects</topic><topic>CYP1</topic><topic>Cytochrome P-450 CYP1A1 - metabolism</topic><topic>Cytochrome P-450 CYP1B1</topic><topic>DNA Damage</topic><topic>DNA strand break</topic><topic>Environmental impact</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Genetics of eukaryotes. Biological and molecular evolution</topic><topic>Halogenated Diphenyl Ethers - administration & dosage</topic><topic>Halogenated Diphenyl Ethers - toxicity</topic><topic>Human exposure</topic><topic>Humans</topic><topic>Hydro-Lyases - metabolism</topic><topic>Medical sciences</topic><topic>Metabolism</topic><topic>Mutagens - toxicity</topic><topic>Oxidative stress</topic><topic>Oxidative Stress - drug effects</topic><topic>Polycyclic aromatic hydrocarbons</topic><topic>Toxicity</topic><topic>Toxicology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>An, Jing</creatorcontrib><creatorcontrib>Yin, Lingling</creatorcontrib><creatorcontrib>Shang, Yu</creatorcontrib><creatorcontrib>Zhong, Yufang</creatorcontrib><creatorcontrib>Zhang, Xinyu</creatorcontrib><creatorcontrib>Wu, Minghong</creatorcontrib><creatorcontrib>Yu, Zhiqiang</creatorcontrib><creatorcontrib>Sheng, Guoying</creatorcontrib><creatorcontrib>Fu, Jiamo</creatorcontrib><creatorcontrib>Huang, Yuecheng</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Environment Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>Environment Abstracts</collection><collection>Pollution Abstracts</collection><jtitle>Mutation research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>An, Jing</au><au>Yin, Lingling</au><au>Shang, Yu</au><au>Zhong, Yufang</au><au>Zhang, Xinyu</au><au>Wu, Minghong</au><au>Yu, Zhiqiang</au><au>Sheng, Guoying</au><au>Fu, Jiamo</au><au>Huang, Yuecheng</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The combined effects of BDE47 and BaP on oxidatively generated DNA damage in L02 cells and the possible molecular mechanism</atitle><jtitle>Mutation research</jtitle><addtitle>Mutat Res</addtitle><date>2011-04-03</date><risdate>2011</risdate><volume>721</volume><issue>2</issue><spage>192</spage><epage>198</epage><pages>192-198</pages><issn>1383-5718</issn><issn>0027-5107</issn><eissn>1879-3592</eissn><abstract>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.</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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