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金属蛋白酶对大菱鲆血清抗氧化酶活性及丙二醛含量的影响
引用本文:李杜文,华智杰,张文香,任海,张玉,靳晓敏,高桂生,李佩国.金属蛋白酶对大菱鲆血清抗氧化酶活性及丙二醛含量的影响[J].海洋科学,2019,43(4):52-60.
作者姓名:李杜文  华智杰  张文香  任海  张玉  靳晓敏  高桂生  李佩国
作者单位:河北科技师范学院 动物科技学院, 河北 秦皇岛 066600;内蒙古农业大学 动物科学学院, 内蒙古 呼和浩特 010000;河北科技师范学院 动物科技学院,河北 秦皇岛,066600;内蒙古农业大学 动物科学学院,内蒙古 呼和浩特,010000
基金项目:国家自然科学基金项目(31502187);河北省自然科学基金项目(C2018407049);河北科技师范学院博士基金项目(2015YB003)
摘    要:为了研究金属蛋白酶对大菱鲆(Scophthalmus maximus)抗氧化系统的影响,作者分别对大菱鲆肌肉注射不同浓度的金属蛋白酶,并于3、6、12、24、48、72 h测定血清中谷胱甘肽过氧化物酶(GSH-Px)、过氧化氢酶(CAT)、总超氧化物歧化酶(T-SOD)、总抗氧化活力(T-AOC)以及丙二醛(MDA)含量变化。结果显示,低质量浓度组(0.037mg/mL)金属蛋白酶处理后,CAT和T-SOD活力除3h显著高于对照组外(P0.05),其余时间点均与对照组无显著差异(P0.05),而低浓度组GSH-Px和T-AOC在整个试验过程中均与对照组无显著性差异(P0.05)。中质量浓度组(0.073mg/mL)金属蛋白酶胁迫后血清中CAT、GSH-Px、T-SOD和T-AOC在3 h~72 h均呈现波浪形的变化趋势。高质量浓度组(0.147 mg/mL)金属蛋白酶对上述4种抗氧化酶产生不同程度的抑制,且在6 h~72 h均显著低于对照组(P0.05)。金属蛋白酶低质量浓度和中质量浓度组MDA含量呈现较为平稳的变化趋势,且与对照组无显著性差异(P0.05),而高质量浓度组MDA含量在3 h~72 h均显著高于对照组(P0.05)。

关 键 词:金属蛋白酶  大菱鲆(Scophthalmusmaximus)  血清  抗氧化指标  丙二醛
收稿时间:2018/9/28 0:00:00
修稿时间:2018/12/8 0:00:00

Effects of metalloprotease on antioxidant system enzyme activities and malondialdehyde content in the serum of Scophthalmus maximus
LI Du-wen,HUA Zhi-jie,ZHANG Wen-xiang,REN Hai,ZHANG Yu,JIN Xiao-min,GAO Gui-sheng and LI Pei-guo.Effects of metalloprotease on antioxidant system enzyme activities and malondialdehyde content in the serum of Scophthalmus maximus[J].Marine Sciences,2019,43(4):52-60.
Authors:LI Du-wen  HUA Zhi-jie  ZHANG Wen-xiang  REN Hai  ZHANG Yu  JIN Xiao-min  GAO Gui-sheng and LI Pei-guo
Institution:The College of Animal Science and Technology, Hebei Normal University of Science and Technology, Qinhuangdao 066600, China;The College of Animal Science, Inner Mongolia Agricultural University, Huhhot 010000, China,The College of Animal Science and Technology, Hebei Normal University of Science and Technology, Qinhuangdao 066600, China,The College of Animal Science and Technology, Hebei Normal University of Science and Technology, Qinhuangdao 066600, China,The College of Animal Science and Technology, Hebei Normal University of Science and Technology, Qinhuangdao 066600, China,The College of Animal Science, Inner Mongolia Agricultural University, Huhhot 010000, China,The College of Animal Science and Technology, Hebei Normal University of Science and Technology, Qinhuangdao 066600, China,The College of Animal Science and Technology, Hebei Normal University of Science and Technology, Qinhuangdao 066600, China and The College of Animal Science and Technology, Hebei Normal University of Science and Technology, Qinhuangdao 066600, China
Abstract:A metalloprotease was purified from the extracellular products (ECP) of Vibrio anguillarum. It was lethal to S. maximus when injected intramuscularly. However, there is little information about the effects of metalloprotease on the antioxidant system and lipid peroxidation in S. maximus. In this study, we measured catalase (CAT), glutathione peroxidase (GSH-Px), total antioxidation activity (T-AOC), total superoxide dismutase (T-SOD) activity, and malondialdehyde (MDA) content in the serum of S. maximus exposed to 0.037 mg/mL, 0.073 mg/mL, or 0.147 mg/mL metalloprotease, respectively, at 3, 6, 12, 24, 48, and 72 hours. The results showed that compared with the control group, the activities of CAT and T-SOD were not significantly different at any of the tested time points, except for 3 h (P>0.05). The variation in GSH-Px and T-AOC was not obvious in the serum of the low-concentration group. The changes in CAT, GSH-Px, T-SOD, and T-AOC in the serum of the medium-concentration group after metalloproteinase stress undulated between 3 h and 72 h. Metalloproteinase in the high-concentration group was inhibited by the above four antioxidant enzymes and was significantly lower than in the control group from 6 h to 72 h. The MDA content of the low- and medium-concentration groups was not significantly different between 3 h and 72 h (P>0.05), while the MDA content of the high-concentration group was significantly higher than that of the control group from 3 h to 72 h (P<0.05).
Keywords:metalloprotease  Scophthalmus maximus  serum  antioxidant indexes  malondialdehyde
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