2007-Antioxidant responses to benzo[a]pyrene, tributyltin and their mixture in the(例子,使用).pdfVIP

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2007-Antioxidant responses to benzo[a]pyrene, tributyltin and their mixture in the(例子,使用).pdf

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2007-Antioxidant responses to benzo[a]pyrene, tributyltin and their mixture in the(例子,使用)

Journal of Environmental Sciences 19(2007) 1129–1135 Antioxidant responses to benzo[a]pyrene, tributyltin and their mixture in the spleen of Sebasticus marmoratus WU Yu-qiong1,2, WANG Chong-gang1, WANG Yun1, ZHAO Yang1, CHEN Yi-xin1, ZUO Zheng-hong1,? 1. Key Laboratory of the Ministry of Education for Cell Biology and Tumor Cell Engineering, School of Life Sciences, Xiamen University, Xiamen 361005, China. E-mail: wyq93042@163.com 2. Bioengineering Department, MinBei Vocational and Technical College, Jianyang 354200, China Received 21 November 2006; revised 5 December 2006; accepted 18 January 2007 Abstract It has been reported that there is an interaction between Benzo[a]pyrene (BaP), a widespread carcinogenic polycyclic aromatic hydrocarbon, and tributyltin (TBT), an organometal used as an antifouling biocide. This study was therefore designed to examine the potential in vivo influence of BaP, TBT and their mixture on splenic antioxidant defense systems of Sebastiscus marmoratus. The fish were exposed to water containing environmentally relevant concentrations of BaP, TBT and their mixture. Spleens were collected for biochemical analysis after exposure for 7, 25, 50 d and after recovery for 7, 20 d. Cotreatment with BaP and TBT for 7 d potentiated the induction of glutathione peroxidase (GPx) activity by BaP or TBT alone. The cotreatment for 25 and 50 d resulted in inhibition of GPx activity, which was similar to the effect of TBT. Splenic glutathione S-transferase (GST) activities were significantly elevated in S. marmoratus exposed to BaP starting from 7 d and remained high up to 25 d. However, no further activity change was found with prolonged exposure. Cotreatment of BaP and TBT primarily inhibited the GST activity, which was similar to the effect of TBT. Cotreatment with BaP and TBT for 25 or 50 d potentiated the depletion of GSH (glutathione) by BaP or TBT alone. MDA (malondialdehyde) contents in spleen of S. marmoratus were not significantly altered compar