符许娟, 黄进强, 李永娟, 吴深基, 赵璐, 孙同振. 碱性环境下急性氨氮胁迫对虹鳟抗氧化能力和非特异性免疫的影响[J]. 水生生物学报. DOI: 10.7541/2024.2024.0074
引用本文: 符许娟, 黄进强, 李永娟, 吴深基, 赵璐, 孙同振. 碱性环境下急性氨氮胁迫对虹鳟抗氧化能力和非特异性免疫的影响[J]. 水生生物学报. DOI: 10.7541/2024.2024.0074
FU Xu-Juan, HUANG Jin-Qiang, LI Yong-Juan, WU Shen-Ji, ZHAO Lu, SUN Tong-Zhen. ACUTE AMMONIA NITROGEN STRESS ON ANTIOXIDANT CAPACITY AND NON-SPECIFIC IMMUNE OF RAINBOW TROUT (ONCORHYNCHUS MYKISS) IN AN ALKALINE ENVIRONMENT[J]. ACTA HYDROBIOLOGICA SINICA. DOI: 10.7541/2024.2024.0074
Citation: FU Xu-Juan, HUANG Jin-Qiang, LI Yong-Juan, WU Shen-Ji, ZHAO Lu, SUN Tong-Zhen. ACUTE AMMONIA NITROGEN STRESS ON ANTIOXIDANT CAPACITY AND NON-SPECIFIC IMMUNE OF RAINBOW TROUT (ONCORHYNCHUS MYKISS) IN AN ALKALINE ENVIRONMENT[J]. ACTA HYDROBIOLOGICA SINICA. DOI: 10.7541/2024.2024.0074

碱性环境下急性氨氮胁迫对虹鳟抗氧化能力和非特异性免疫的影响

ACUTE AMMONIA NITROGEN STRESS ON ANTIOXIDANT CAPACITY AND NON-SPECIFIC IMMUNE OF RAINBOW TROUT (ONCORHYNCHUS MYKISS) IN AN ALKALINE ENVIRONMENT

  • 摘要: 为探究碱性环境下急性氨氮胁迫对虹鳟(Oncorhynchus mykiss)抗氧化和免疫功能的影响, 研究设置3个不同氨氮处理组(0.86、1.73和2.59 mg/L)对虹鳟进行96h急性胁迫实验, 测定肝脏和血清中抗氧化与免疫酶的活性及肝脏中相关基因的表达水平。结果显示, 在不同浓度氨氮胁迫下, 虹鳟肝脏CAT、T-AOC、T-SOD活性和MDA含量均呈现先上升后下降的变化趋势, 血清T-AOC活性呈先下降后上升的变化, 其他酶活性变化则与肝脏一致; 高浓度组肝脏MDA含量在胁迫48h时最低, 而T-SOD活性最高。肝脏和血清免疫相关酶GPT、GOT、ACP和AKP的活性在不同浓度的氨氮胁迫下呈先升高后降低的变化趋势; 在96h时, 不同浓度组肝脏和血清中GPT活性均显著高于对照组(P<0.05)。不同浓度组肝脏抗氧化相关基因(cu/zn-sodmn-sodcat)表达量在6h时均高于对照组; 在12h时, hsp90基因的表达量高于对照组, 而hsp70基因的表达量低于对照组。以上结果表明, 在胁迫初期虹鳟抗氧化和免疫酶活性被诱导激活, 抗氧化与免疫相关基因表达量上调; 随着胁迫时间的延长, 机体抗氧化与免疫功能受到抑制, 相关酶活性与基因表达量下调。研究为深入探究虹鳟氨氮胁迫下抗氧化和免疫系统的应激机制提供了基础资料。

     

    Abstract: In order to investigate the effects of acute ammonia nitrogen stress on the antioxidant and immune function of rainbow trout (Oncorhynchus mykiss) in an alkaline environment, fish were exposed to three different concentrations of ammonia nitrogen (0.86, 1.73, and 2.59 mg/L) for up to 96h. We measured the activities of antioxidant enzymes (CAT, T-AOC, T-SOD, and MDA) and immune enzymes (ACP, AKP, GOT, and GPT) in the liver and serum, as well as the expression levels of related genes in the liver. The results showed that antioxidant enzyme activity in the liver increased from 0 to 6h and then decreased, while T-AOC activity in the serum exhibited a trend of decreasing followed by increasing under different concentrations of ammonia nitrogen stress. At 48h, MDA content was the lowest and T-SOD activity was the highest with the high concentration group in the liver. In the different concentration groups, immune enzyme activity increased from 0 to 6h and then gradually decreased in both liver and serum. At 96h, GPT activity was significantly higher than that of the control group (P<0.05) in both liver and serum. In the low, medium, and high concentration groups, the expression levels of antioxidant related genes (cu/zn-sod, mn-sod, and cat) were higher than those of the control group at 6h in the liver. At 12h, the expression of the immune related gene hsp90 was higher than that of the control group, whereas hsp70 showed the opposite trend. These results indicated that antioxidant and immune enzyme activities were induced, and the expression of related gene was upregulated at the early stage of stress. With prolonged stress, antioxidant and immune functions were inhibited, as evidenced by the downregulation of enzyme activities and gene expressions. This study provides fundamental information for further investigation on the stress mechanisms of antioxidant and immune systems in rainbow trout under ammonia nitrogen stress.

     

/

返回文章
返回