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绿原酸诱导凡纳滨对虾抗氧化功能及抵御低盐度胁迫的响应
引用本文:王芸,李健,李正,牛津,王珺,黄忠,林黑着.绿原酸诱导凡纳滨对虾抗氧化功能及抵御低盐度胁迫的响应[J].中国水产科学,2014,21(2):340-350.
作者姓名:王芸  李健  李正  牛津  王珺  黄忠  林黑着
作者单位:1. 农业部水产品加工重点实验室 中国水产科学研究院 南海水产研究所, 广东 广州 510300;2. 农业部海洋渔业可持续发展重点实验室 中国水产科学研究院 黄海水产研究所, 山东 青岛 266071; 3. 建明工业(珠海)有限公司, 广东 珠海 519040
基金项目:农业部水产品加工重点实验室开放基金课题 (nybjg201205); 中央级公益性科研院所基本科研业务费专项资金(中国水产科学研究院南海水产研究所)资助项目 (2011TS05, 2013TS03).
摘    要:

选择健康、均匀, 体质量为(6.74 ± 0.08) g的凡纳滨对虾(Litopenaeus vannamei),  360尾随机分为4, 分别投喂含有0 mg/kg100 mg/kg200 mg/kg400 mg/kg绿原酸的饲料28 d, 随后将对虾从盐度为32的天然海水直接转移至盐度为10的海水中暴露72 h, 测定对虾肝胰腺TASGPxCAT活力和GPxCAT基因表达水平。结果显示, 在天然海水养殖条件下, 绿原酸对凡纳滨对虾肝胰腺TASGPx活性无明显影响, 但投喂含有绿原酸的饲料28 d, 对虾肝胰腺GPxCATGPxCAT基因表达水平显著高于D0(P<0.05), D2GPx活性和GPxCAT基因表达水平最高, 分别为164.29 U/mgprot1.612.14。低盐度胁迫24 h, D0组对虾抗氧化反应表现在TASGPx活性和GPx基因表达水平较28 d显著升高(P<0.05), 分别增加了31.30%27.96%170%, 而绿原酸各组对虾肝胰腺TASGPx活性和GPx基因表达水平显著低于D0(P<0.05), 说明绿原酸可有效缓解低盐度胁迫下对虾抗氧化系统酶活性的剧烈波动。低盐度胁迫72 h, 绿原酸各组对虾肝胰腺TASGPxCAT活性及CAT基因表达水平均明显高于D0。上述结果表明绿原酸能够诱导凡纳滨对虾的抗氧化系统功能, 在凡纳滨对虾抵抗低盐度胁迫中发挥着重要的作用。本研究旨为开发绿色植物提取物在对虾养殖中的应用, 解决盐度胁迫对机体造成的氧化损伤提供理论依据。



关 键 词:绿原酸    凡纳滨对虾    抗氧化系统功能    盐度胁迫    肝胰腺    酶活性
修稿时间:2015/7/16 0:00:00

Antioxidant activity and resistance to low-salinity stress in Litopenaeus vannamei induced by chlorogenic acid
WANG Yun,LI Jian,LI Zheng,NIU Jin,WANG Jun,HUANG Zhong,LIN Heizhao.Antioxidant activity and resistance to low-salinity stress in Litopenaeus vannamei induced by chlorogenic acid[J].Journal of Fishery Sciences of China,2014,21(2):340-350.
Authors:WANG Yun  LI Jian  LI Zheng  NIU Jin  WANG Jun  HUANG Zhong  LIN Heizhao
Institution:1. Key Laboratory of Aquatic Product Processing, Ministry of Agriculture, South China Sea Fisheries Research Institute, Chinese Academy of Fishery Sciences, Guangzhou 510300, China;2. Key Laboratory for Sustainable Development of Marine Fisheries, Ministr
Abstract:

To investigate the effects of chlorogenic acid on the antioxidant activity and resistance to low-salinity stress in Litopenaeus vannamei, 360 shrimps were randomly divided into four groups and fed four diets containing 0, 100, 200 and 400 mg chlorogenic acid/kg(diet). After feeding for 28 days, all shrimps were subjected to an acute salinity change from 32 to 10 for 72 h. Total antioxidant status (TAS), glutathione peroxidase (GPx) and catalase (CAT) levels, and expression of the GPx and CAT genes in the hepatopancreas of L. vannamei, were analyzed. The results demonstrated that supplemental chlorogenic acid had no effect on TAS or on GPx activity in the hepatopancreas when shrimp were cultured in natural seawater. Compared with the D0 control group, however, dietary supplemental chlorogenic acid significantly increased GPx and CAT activities, and expression of the GPx and CAT gene in the hepatopancreas after feeding the shrimp for 28 days (P<0.05). GPx activity and gene expressions of GPx and CAT in the D2 group 200 mg (chlorogenic acid)/kg(diet) ] were higher than in the other groups, at 164.29 U/mg(prot) and 1.61 and 2.14 fold, respectively. After low-salinity stress for 24 h, the antioxidant response was characterized by higher TAS, greater GPx activity and higher gene expression of GPx in the hepatopancreas compared with levels found at 28 days (P<0.05), i.e. an increase of 31.30%, 27.96% and 170%, respectively. Moreover, TAS, GPx activity and GPx gene expression in the hepatopancreas in shrimp that were fed diets supplemented with chlorogenic acid were lower than those of the D0 group (P<0.05). The results indicate that chlorogenic acid could effectively inhibit dramatic changes in antioxidant enzyme system activities of shrimp exposed to low-salinity stress. After low-salinity stress for 72 h, TAS, GPx and CAT activities and GPx gene expression in the hepatopancreas of shrimp that were fed chlorogenic acid were higher than the D0 group. In conclusion, chlorogenic acid induces antioxidant system activity and plays an important role in resistance to low-salinity stress in L. vannamei.

Keywords:chlorogenic acid  Litopenaeus vannamei  antioxidant system  salinity stress  hepatopancreas  enzymatic activity
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