{"title":"淡水鱼类过氧化氢酶活性对金属的响应","authors":"","doi":"10.34091/ajls.3.2.6","DOIUrl":null,"url":null,"abstract":"Catalase activity in response to binary metal mixture of Zn + Ni was studied in gills, hepatic, renal and cardiac tissues of Catla catla. A total of 30 fish fingerlings were kept in two glass aquaria (15 in controlled condition and 15 in metal mixture containing aquarium) for the period of two weeks. After the completion of the trial period, fish were dissected for different organ collection. The extracted organs were homogenized in phosphate buffer (50 mM; pH 7.0). The activity of catalase was determined by absorption at 240 nm by using the standard methods. The inferences showed higher catalase activity in liver (223.33 ±1 UmL-1), kidney (163.33 ± 0.7 UmL-1), gills (123.33 ±0.9 UmL-1) and cardiac (120 ±3 UmL-1) tissues of Zn + Ni treated fish in comparison to controlled fish liver (116.66 ±2 UmL-1), kidney (101.66 ±1 UmL-1), gills (96.66 ±0.66 UmL-1) and cardiac tissues (70 ±0.33 UmL-1) in this study. Statistically, significant differences at p ≤ 0.05 was observed for catalase activity between Zn + Ni stressed and control fish groups. While, in different organs of both group of fishes the catalase activity order was observed as hepatic > renal > gills > heart. Findings of this study would be helpful in monitoring aquatic ecosystems using fish antioxidant system which acts as a bio-indicator of metal contamination.","PeriodicalId":371643,"journal":{"name":"Abasyn Journal Life Sciences","volume":"1 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2020-12-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Catalase Activity in Response to Metals in Freshwater Fish Catla catla\",\"authors\":\"\",\"doi\":\"10.34091/ajls.3.2.6\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Catalase activity in response to binary metal mixture of Zn + Ni was studied in gills, hepatic, renal and cardiac tissues of Catla catla. A total of 30 fish fingerlings were kept in two glass aquaria (15 in controlled condition and 15 in metal mixture containing aquarium) for the period of two weeks. After the completion of the trial period, fish were dissected for different organ collection. The extracted organs were homogenized in phosphate buffer (50 mM; pH 7.0). The activity of catalase was determined by absorption at 240 nm by using the standard methods. The inferences showed higher catalase activity in liver (223.33 ±1 UmL-1), kidney (163.33 ± 0.7 UmL-1), gills (123.33 ±0.9 UmL-1) and cardiac (120 ±3 UmL-1) tissues of Zn + Ni treated fish in comparison to controlled fish liver (116.66 ±2 UmL-1), kidney (101.66 ±1 UmL-1), gills (96.66 ±0.66 UmL-1) and cardiac tissues (70 ±0.33 UmL-1) in this study. Statistically, significant differences at p ≤ 0.05 was observed for catalase activity between Zn + Ni stressed and control fish groups. While, in different organs of both group of fishes the catalase activity order was observed as hepatic > renal > gills > heart. Findings of this study would be helpful in monitoring aquatic ecosystems using fish antioxidant system which acts as a bio-indicator of metal contamination.\",\"PeriodicalId\":371643,\"journal\":{\"name\":\"Abasyn Journal Life Sciences\",\"volume\":\"1 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2020-12-31\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Abasyn Journal Life Sciences\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.34091/ajls.3.2.6\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Abasyn Journal Life Sciences","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.34091/ajls.3.2.6","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
研究了鲶鱼鳃、肝脏、肾脏和心脏组织过氧化氢酶活性对锌+镍二元金属混合物的响应。在2个玻璃水族箱中(控制水族箱15只,金属混合水族箱15只)饲养30只鱼种,为期2周。试验期结束后,对鱼进行解剖,收集不同的器官。提取的器官在磷酸盐缓冲液(50 mM;pH值7.0)。用标准方法在240 nm处吸收测定过氧化氢酶活性。结果表明,锌+ Ni处理后的鱼肝脏(223.33±1 μ l -1)、肾脏(163.33±0.7 μ l -1)、鱼鳃(123.33±0.9 μ l -1)和心脏(120±3 μ l -1)过氧化氢酶活性高于对照组的肝脏(116.66±2 μ l -1)、肾脏(101.66±1 μ l -1)、鱼鳃(96.66±0.66 μ l -1)和心脏(70±0.33 μ l -1)。Zn + Ni胁迫组与对照组过氧化氢酶活性差异显著(p≤0.05)。而在两组鱼的不同器官中,过氧化氢酶活性依次为肝脏>肾脏>鳃>心脏。本研究结果将有助于利用鱼类抗氧化系统作为金属污染的生物指示物对水生生态系统进行监测。
Catalase Activity in Response to Metals in Freshwater Fish Catla catla
Catalase activity in response to binary metal mixture of Zn + Ni was studied in gills, hepatic, renal and cardiac tissues of Catla catla. A total of 30 fish fingerlings were kept in two glass aquaria (15 in controlled condition and 15 in metal mixture containing aquarium) for the period of two weeks. After the completion of the trial period, fish were dissected for different organ collection. The extracted organs were homogenized in phosphate buffer (50 mM; pH 7.0). The activity of catalase was determined by absorption at 240 nm by using the standard methods. The inferences showed higher catalase activity in liver (223.33 ±1 UmL-1), kidney (163.33 ± 0.7 UmL-1), gills (123.33 ±0.9 UmL-1) and cardiac (120 ±3 UmL-1) tissues of Zn + Ni treated fish in comparison to controlled fish liver (116.66 ±2 UmL-1), kidney (101.66 ±1 UmL-1), gills (96.66 ±0.66 UmL-1) and cardiac tissues (70 ±0.33 UmL-1) in this study. Statistically, significant differences at p ≤ 0.05 was observed for catalase activity between Zn + Ni stressed and control fish groups. While, in different organs of both group of fishes the catalase activity order was observed as hepatic > renal > gills > heart. Findings of this study would be helpful in monitoring aquatic ecosystems using fish antioxidant system which acts as a bio-indicator of metal contamination.