Abrupt salinity stress induces oxidative stress via the Nrf2-Keap1 signaling pathway in large yellow croaker Pseudosciaena crocea

被引:0
作者
Lin Zeng
Chun-Xiang Ai
Yong-Hong Wang
Jian-She Zhang
Chang-Wen Wu
机构
[1] Zhejiang Ocean University,National Engineering Research Center for Marine Aquaculture
[2] Xiamen University,College of Ocean and Earth Sciences
来源
Fish Physiology and Biochemistry | 2017年 / 43卷
关键词
Salinity stress; Antioxidant enzyme; Nrf2–Keap1;
D O I
暂无
中图分类号
学科分类号
摘要
The aim of the present study was to evaluate the effects of abrupt salinity stress (12, 26 (control), and 40) on lipid peroxidation, activities and mRNA levels of antioxidant enzymes (Cu/Zn-SOD, CAT, GPx, and GR), and gene expression of the Nrf2-Keap1 signaling molecules at different times (6, 12, 24, and 48 h) in the liver of large yellow croaker Pseudosciaena crocea. The results showed that lipid peroxidation was sharply reduced at 6 h and increased at 12 h before returning to control levels in the hypo-salinity group. Similarly, lipid peroxidation was significantly decreased at 6 h followed by a sharp increase towards the end of the exposure in the hyper-salinity group. Negative relationships between lipid peroxidation and antioxidant enzyme activities and positive relationships between activities and gene expression of antioxidant enzymes were observed, suggesting that the changes at molecular levels and enzyme activity levels may provide protective roles against damage from salinity stress. Obtained results also showed a coordinated transcriptional regulation of antioxidant genes, suggesting that Nrf2 is required for regulating these genes. Furthermore, there was a positive relationship between the mRNA levels of Nrf2 and Keap1, indicating that Keap1 plays an important role in switching off the Nrf2 response. In conclusion, this is the first study to elucidate effects of salinity stress on antioxidant responses in large yellow croaker through the Keap1–Nrf2 pathway.
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页码:955 / 964
页数:9
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共 138 条
[1]  
Aebi H(1984)[13] Catalase in vitro Method Enzymol 105 121-126
[2]  
Beauchamp C(1971)Superoxide dismutase: improved assays and an assay applicable to acrylamide gels Anal Biochem 44 276-287
[3]  
Fridovich I(1976)A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding Anal Biochem 72 248-254
[4]  
Bradford MM(2008)Molecular characterization and mRNA expression of glutathione peroxidase and glutathione S-transferase during osmotic stress in olive flounder ( Comp Biochem Phys A 149 330-337
[5]  
Choi CY(1989)) Environ Toxicol Chem 8 1103-1123
[6]  
An KW(2015)Biochemical responses in aquatic animals: a review of determinants of oxidative stress Biochem J 469 347-355
[7]  
An MI(1985)KEAP1–NRF2 signalling and autophagy in protection against oxidative and reductive proteotoxicity Plant Sci 42 35-40
[8]  
Di Giulio RT(2007)Evidence for glutathione peroxidase activities in cultured plant cells FEBS J 274 5790-5798
[9]  
Washburn PC(2014)Osmotic stress sensing and signaling in fishes Aquat Toxicol 150 117-123
[10]  
Wenning RJ(2006)Identification of the Nrf2–Keap1 pathway in the European eel Hepatology 43 144-153