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大型溞暴露于布洛芬后CYP360A、CYP314和谷胱甘肽S-转移酶的基因反应及整体生物变化

Gene response of CYP360A, CYP314, and GST and whole-organism changes in Daphnia magna exposed to ibuprofen.

作者信息

Wang Lan, Peng Ying, Nie Xiangping, Pan Benben, Ku Peijia, Bao Shuang

机构信息

Department of Ecology/Institute of Hydrobiology, Jinan University, Guangzhou 510632,China.

Department of Ecology/Institute of Hydrobiology, Jinan University, Guangzhou 510632,China; Key Laboratory of Eutrophication and Red Tide Prevention of Guangdong Higher Education Institutes, Jinan University, Guangzhou 510632, China.

出版信息

Comp Biochem Physiol C Toxicol Pharmacol. 2016 Jan;179:49-56. doi: 10.1016/j.cbpc.2015.08.010. Epub 2015 Sep 3.

Abstract

The fate and ecological impact of non-steroidal anti-inflammatory drugs (NSAIDs) in aquatic environments has gained increasingly concern recently. However, limited information is provided about the toxicity mechanism of NSAIDs to aquatic invertebrates. In the present study, we investigated the expression of CYP360A, CYP314, and GST genes involved in the detoxification process and the responses of their associated enzymes activity, as well as whole-organism changes in Daphnia magna exposed to environmentally relevant concentrations of ibuprofen (IBU). Results showed that the total amount of eggs produced per female, total number of brood per female, and body length were significantly decreased under IBU exposure, suggesting the effects of chronic IBU exposure on growth and reproduction of D. magna cannot be ignored. In gene expression level, the CYP360A gene, homologue to CYP3A in mammalian, showed inhibition at low concentration of IBU (0.5μg·L(-1)) and induction at high concentration of IBU (50μg·L(-1)). GST gene also exhibited a similar performance to CYP3A. CYP314 displayed inhibition for short time exposure (6h) and induced with prolonged exposure time (48h) at low concentration of IBU (0.5μg·L(-1)). Erythromycin N-demethylase (ERND) and aminopyrine N-demethylase (APND) related to cytochrome oxidase P450 (CYPs) were inhibited for short time exposure (6h) to IBU and then activated with prolonged exposure time (48h) at low concentration of IBU (0.5μg·L(-1)), while EROD showed a dose-dependent pattern under IBU exposure. As for antioxidative system, induction of glutathione S-transferase (GST), superoxide dismutase (SOD), and catalase (CAT) was observed in short-term exposure to IBU. Meanwhile, methane dicarboxylic aldehyde (MDA) content increased with the increasing IBU concentration and the delayed exposure time, displaying obvious dose- and time-dependent pattern. In summary, IBU significantly altered some physiological and biochemical parameters and genes expressions associated with detoxification metabolism in D. magna, the integrated approach combining the response in molecule levels with the performance of the whole organism can help elucidate the toxic effects of IBU and provide more insight into the exact mechanism of toxicity in aquatic organisms.

摘要

非甾体抗炎药(NSAIDs)在水生环境中的归宿及其生态影响近来日益受到关注。然而,关于NSAIDs对水生无脊椎动物的毒性机制,所提供的信息有限。在本研究中,我们调查了参与解毒过程的CYP360A、CYP314和GST基因的表达情况及其相关酶活性的变化,以及暴露于环境相关浓度布洛芬(IBU)下的大型溞的整体生物体变化。结果表明,在IBU暴露下,每只雌性产生的卵总数、每只雌性的产卵次数和体长均显著降低,这表明慢性IBU暴露对大型溞生长和繁殖的影响不容忽视。在基因表达水平上,与哺乳动物CYP3A同源的CYP360A基因,在低浓度IBU(0.5μg·L(-1))时表现出抑制作用,而在高浓度IBU(50μg·L(-1))时表现出诱导作用。GST基因也表现出与CYP3A类似的情况。在低浓度IBU(0.5μg·L(-1))下,CYP314在短时间暴露(6小时)时表现出抑制作用,而随着暴露时间延长(48小时)则表现出诱导作用。与细胞色素氧化酶P450(CYPs)相关的红霉素N-脱甲基酶(ERND)和氨基比林N-脱甲基酶(APND)在低浓度IBU(0.5μg·L(-1))短时间暴露(6小时)时受到抑制,随后随着暴露时间延长(48小时)而被激活,而EROD在IBU暴露下呈现剂量依赖性模式。至于抗氧化系统,在短期暴露于IBU时观察到谷胱甘肽S-转移酶(GST)、超氧化物歧化酶(SOD)和过氧化氢酶(CAT)的诱导。同时,随着IBU浓度的增加和暴露时间的延长,丙二醛(MDA)含量增加,呈现出明显的剂量和时间依赖性模式。总之,IBU显著改变了大型溞一些与解毒代谢相关的生理生化参数和基因表达,将分子水平的反应与整体生物体的表现相结合的综合方法有助于阐明IBU的毒性作用,并为深入了解水生生物的毒性确切机制提供更多见解。

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