Zheng Jia-Lang, Zeng Lin, Shen Bin, Xu Mei-Ying, Zhu Ai-Yi, Wu Chang-Wen
National Engineering Research Center of Marine Facilities Aquaculture, Zhejiang Ocean University, Zhoushan 316022, PR China.
National Engineering Research Center of Marine Facilities Aquaculture, Zhejiang Ocean University, Zhoushan 316022, PR China.
Fish Shellfish Immunol. 2016 May;52:1-8. doi: 10.1016/j.fsi.2016.02.031. Epub 2016 Mar 3.
We evaluated the effects of acute Zn exposure (4 and 8 mg L(-1) Zn) on lipid peroxidation, and activities and mRNA levels of antioxidant enzyme genes (Cu/Zn-SOD, CAT, GPx, and GR), and gene expression of the Nrf2-Keap1 signaling molecule at different exposure times (0, 6, 12, 24, 48, and 96 h) in the spleen of large yellow croaker. Lipid peroxidation remained relatively constant during 6-48 h and 6-24 h and sharply increased at 96 h and during 48-96 h in fish exposed to 4 and 8 mg L(-1) Zn, respectively. Activities of all tested enzymes increased during the early stage of exposure and decreased towards the end of the exposure in both groups. However, mRNA levels of antioxidant enzyme genes were dramatically up-regulated by 4 and 8 mg L(-1) Zn during the late stage of exposure. During the early stage of exposure for 6 h, the 8 mg L(-1) Zn exposure sharply increased mRNA levels of Cu/Zn-SOD, CAT, GPx1b, Nrf2, and Keap1, whereas, the 4 mg L(-1) Zn exposure did not significantly affect the expression of these genes. Our data also showed positive relationships between Nrf2 expression and mRNA levels of its target genes, suggesting that Nrf2 was required for the protracted induction of these genes. Furthermore, a sharp increase in Keap1 expression levels was observed in fish exposed to 4 mg L(-1) at 96 h, and 8 mg L(-1) at 6, 48, and 96 h. In conclusion, the present study demonstrated that Zn-induced antioxidant defenses were involved in modifications at enzymatic and transcriptional levels and the transcriptional regulation of the Nrf2-Keap1 signaling molecule; these results may contribute to the understanding of mechanisms that maintain the correct redox balance in the immune organ of the large yellow croaker.
我们评估了急性锌暴露(4和8 mg L(-1)锌)对大黄鱼脾脏脂质过氧化、抗氧化酶基因(铜/锌超氧化物歧化酶、过氧化氢酶、谷胱甘肽过氧化物酶和谷胱甘肽还原酶)活性及mRNA水平,以及Nrf2-Keap1信号分子在不同暴露时间(0、6、12、24、48和96小时)的基因表达的影响。在暴露于4和8 mg L(-1)锌的鱼中,脂质过氧化在6 - 48小时和6 - 24小时内相对保持稳定,分别在96小时和48 - 96小时急剧增加。两组中所有测试酶的活性在暴露早期增加,在暴露末期降低。然而,抗氧化酶基因的mRNA水平在暴露后期被4和8 mg L(-1)锌显著上调。在暴露6小时的早期阶段,8 mg L(-1)锌暴露使铜/锌超氧化物歧化酶、过氧化氢酶、谷胱甘肽过氧化物酶1b、Nrf2和Keap1的mRNA水平急剧增加,而4 mg L(-1)锌暴露对这些基因的表达没有显著影响。我们的数据还显示Nrf2表达与其靶基因的mRNA水平之间呈正相关,表明Nrf2是这些基因长期诱导所必需的。此外,在暴露于4 mg L(-1)锌96小时以及暴露于8 mg L(-1)锌6、48和96小时的鱼中观察到Keap1表达水平急剧增加。总之,本研究表明锌诱导的抗氧化防御涉及酶和转录水平的修饰以及Nrf2-Keap1信号分子的转录调控;这些结果可能有助于理解维持大黄鱼免疫器官正确氧化还原平衡的机制。