刘薇

个人信息Personal Information

教授

博士生导师

硕士生导师

主要任职:环境学院副院长

其他任职:环境学院教工党支部副书记

性别:女

毕业院校:大连理工大学

学位:博士

所在单位:环境学院

联系方式:Email:Liu_wei@dlut.edu.cn

电子邮箱:liu_wei@dlut.edu.cn

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Oxidative damage and genotoxic effect in mice caused by sub-chronic exposure to low-dose volatile organic compounds

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论文类型:期刊论文

发表时间:2013-04-01

发表刊物:INHALATION TOXICOLOGY

收录刊物:SCIE、PubMed、Scopus

卷号:25

期号:5

页面范围:235-242

ISSN号:0895-8378

关键字:Genotoxicity; mice; oxidative damage; sub-chronic exposure; VOCs

摘要:Volatile organic compounds (VOCs) are widely used as constituents of household chemicals. Although adverse health effects have been reported, long-term exposure to low-level VOCs mixture has not been studied. Especially, there is a lack of substantial information on the sensitive biomarkers and carcinogenic markers. In the present study, we examined oxidative stress and genotoxic effects of sub-chronic low-dose VOCs mixture (formaldehyde, benzene, toluene and xylene). Male Kunming mice were exposed to 0 (control) and three different doses of VOCs mixture (group 1S, 5S and 10S) for 90 d (2 h/d). Group 1S is 0.10, 0.11, 0.20 and 0.20 mg/m(3), group 5S is 0.50, 0.55, 1.00 and 1.00 mg/m(3), group 10S is 1.00, 1.10, 2.00 and 2.00 mg/m(3), which, respectively, corresponded to 1, 5 and 10 times of indoor air quality standard (IAQS) in China. One day following VOCs exposure, oxidative stress markers in lung, 8-hydroxy-2'-deoxyguanosine in bronchoalveolar lavage fluid and genotoxicity (DNA damage) in liver were examined. Results showed that exposure to VOCs (IAQS dose) resulted in oxidative damages of lung, which were supported by the significant changes on reactive oxygen species, reduced glutathione (GSH), GSH S-transferase, total antioxidative capacity, malondialdehyde, protein carbonyl and nitric oxide (NO). Moreover, oxidative stress markers in group 5S and 10S (except NO) in lung were affected significantly. In addition, VOCs exposure also induced significantly DNA damage in liver. Our study suggested long-term VOCs inhalation at low levels caused oxidative stress and genotoxicity response in mice. Since effects were seen at the current IAQS level, further studies below this level are necessary.