A method to measure total antioxidant capacity against peroxyl radicals in aquatic organisms: Application to evaluate microcystins toxicity

被引:360
作者
Amado, Lilian Lund [1 ,2 ]
Garcia, Marcia Longaray [1 ]
Ramos, Patricia Baptista [1 ]
Freitas, Ricardo Franco [1 ]
Zafalon, Bruna [1 ]
Ribas Ferreira, Josencler Luis [1 ,2 ]
Yunes, Joao Sarkis
Monserrat, Jose M. [1 ,2 ]
机构
[1] Univ Fed Rio Grande FURG, Inst Ciencias Biol, BR-96201900 Rio Grande, RS, Brazil
[2] Fundacao Univ Fed Rio Grande, Programa Posgrad Ciencias Fisiol Fisiol Anim Com, Rio Grande, RS, Brazil
关键词
Antioxidant defenses; Total antioxidant capacity; Reactive oxygen species; Fish; Microcystins toxicity; Peroxyl radicals; Ecotoxicology; OXYRADICAL SCAVENGING CAPACITY; LAEONEREIS-ACUTA POLYCHAETA; OXIDATIVE STRESS RESPONSES; CORYDORAS-PALEATUS; CYANOBACTERIAL CELLS; ONCORHYNCHUS-MYKISS; RAINBOW-TROUT; EXPOSURE; HEPATOPANCREAS; DETOXIFICATION;
D O I
10.1016/j.scitotenv.2008.11.038
中图分类号
X [环境科学、安全科学];
学科分类号
083001 [环境科学];
摘要
Determination of total antioxidant capacity, instead of the measurements of limited number of antioxidants, is very important for the understanding of how antioxidants interact with reactive oxygen species (RCIS). Several techniques already exist with this propose, although some of them are extremely time-consuming. A new methodology is proposed, based on the detection of ROS by fluorometry (ex/em: 485/520 nm) employing 2',7'-dichloro fluorescein diacetate (H2DCF-DA) as substrate. Supernatant of homogenized samples from different organs (gill, muscle, liver, and brain) of the teleost fish Jenynsia multidentata (Anaplebidae) were exposed to peroxyl radicals generated by thermal (35 degrees C decomposition of 2,2'-azobis (2 methylpropionamidine) dihydrochloride (ABAP, 4 mM). Different protein concentrations (0.5, 1, 2 and 8 mg/ml) were assayed to get the best signal and curve fitting of fluorescence data over time (30 min). Total antioxidant capacity against peroxyl radicals was estimated as the difference in ROS area with and without ABAP, relative to the fluorescence registered without ABAP. For application of this methodology, J. multidentata specimens were exposed for 24 h to microcystins, cyanotoxins known to induce oxidative stress. Almost all organs showed a lower antioxidant capacity (p<0.05) in samples with 8 mg proteins/ml, when compared to protein content of 1-2 mg/ml. In liver samples, higher (p<0.05) free iron content was determined in samples with 8 mg proteins/ml. Sensitivity test employing GSH spiked in homogenized samples showed the protocol efficiency in detecting total antioxidant capacity. In the test with microcystins a dose-dependent decrease (p<0.05) of antioxidant competence in gills and brain and an inverse result with liver samples were observed. The use of antioxidant defenses was efficient in avoiding oxidative damage, as the content of oxidized proteins was not altered. Data obtained show the potential of this new methodology to be used in ecotoxicological studies. (c) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:2115 / 2123
页数:9
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