Responses of antioxidant status and Na+-K+-ATPase activity in gill of rainbow trout, Oncorhynchus mykiss, chronically treated with carbamazepine
Language English Country Great Britain, England Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
19889442
DOI
10.1016/j.chemosphere.2009.10.031
PII: S0045-6535(09)01224-7
Knihovny.cz E-resources
- MeSH
- Anticonvulsants toxicity MeSH
- Antioxidants metabolism MeSH
- Time Factors MeSH
- Water Pollutants, Chemical toxicity MeSH
- Glutathione metabolism MeSH
- Glutathione Peroxidase metabolism MeSH
- Glutathione Reductase metabolism MeSH
- Carbamazepine toxicity MeSH
- Protein Carbonylation MeSH
- Catalase metabolism MeSH
- Oncorhynchus mykiss metabolism MeSH
- Oxidative Stress MeSH
- Lipid Peroxidation MeSH
- Sodium-Potassium-Exchanging ATPase metabolism MeSH
- Superoxide Dismutase metabolism MeSH
- Gills enzymology MeSH
- Animals MeSH
- Check Tag
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Anticonvulsants MeSH
- Antioxidants MeSH
- Water Pollutants, Chemical MeSH
- Glutathione MeSH
- Glutathione Peroxidase MeSH
- Glutathione Reductase MeSH
- Carbamazepine MeSH
- Catalase MeSH
- Sodium-Potassium-Exchanging ATPase MeSH
- Superoxide Dismutase MeSH
In recent years, chemical pollution by the residual pharmaceuticals has been increasingly important issue due to its widely present in the aquatic environment. However, the toxicological effects of residual pharmaceuticals on fish have not been adequately researched. The aim of this work is to investigate the toxic effect of CBZ, an anticonvulsant drug commonly present in aquatic environment, on antioxidant status and Na+-K+-ATPase in gill of rainbow trout exposed to sublethal CBZ (1.0 microg L(-1), 0.2 mg L(-1) and 2.0 mg L(-1)) for 7, 21 and 42 d. After prolonged exposure of CBZ at higher test concentration (0.2 or 2.0 mg L(-1)), oxidative stress was apparent as reflected by the significant higher LPO and CP levels in fish gill, as well as the significant inhibition of antioxidant enzymes activities including SOD, CAT, GR and GPx. Besides, reduced glutathione level and Na+-K+-ATPase activity were significantly lower than those of the control after 42 d of exposure to CBZ at higher test concentration (0.2 or 2.0 mg L(-1)). The results of this study indicate that chronic exposure of CBZ has altered multiple physiological indices in fish gill; however, before those parameters are used as special biomarkers for monitoring residual pharmaceuticals in aquatic environment, more detailed experiments in laboratory need to be performed in the future.
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