Physiological condition status and muscle-based biomarkers in rainbow trout (Oncorhynchus mykiss), after long-term exposure to carbamazepine
Language English Country England, Great Britain Media print
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
19757490
DOI
10.1002/jat.1482
Knihovny.cz E-resources
- MeSH
- Algorithms MeSH
- Anticonvulsants toxicity MeSH
- Biomarkers metabolism MeSH
- Water Pollutants, Chemical toxicity MeSH
- DNA metabolism MeSH
- Glutathione Peroxidase metabolism MeSH
- Glutathione Reductase metabolism MeSH
- Liver anatomy & histology drug effects MeSH
- Carbamazepine toxicity MeSH
- Protein Carbonylation drug effects MeSH
- Catalase metabolism MeSH
- Muscle, Skeletal drug effects enzymology metabolism MeSH
- Thiobarbituric Acid Reactive Substances metabolism MeSH
- Random Allocation MeSH
- Oncorhynchus mykiss metabolism physiology MeSH
- RNA metabolism MeSH
- Sodium-Potassium-Exchanging ATPase metabolism MeSH
- Superoxide Dismutase metabolism MeSH
- Body Weight drug effects MeSH
- Organ Size drug effects MeSH
- Dose-Response Relationship, Drug MeSH
- Animals MeSH
- Check Tag
- Male MeSH
- Female MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Anticonvulsants MeSH
- Biomarkers MeSH
- Water Pollutants, Chemical MeSH
- DNA MeSH
- Glutathione Peroxidase MeSH
- Glutathione Reductase MeSH
- Carbamazepine MeSH
- Catalase MeSH
- Thiobarbituric Acid Reactive Substances MeSH
- RNA MeSH
- Sodium-Potassium-Exchanging ATPase MeSH
- Superoxide Dismutase MeSH
Recently, residual pharmaceuticals are generally recognized as relevant sources of aquatic environmental pollutants. However, the toxicological effects of these contaminants have not been adequately researched. In this study, the chronic toxic effects of carbamazepine (CBZ), an anticonvulsant pharmaceutical commonly present in surface and ground water, on physiological condition status and muscle-based biomarkers of rainbow trout were investigated. Fish were exposed at sublethal concentrations of CBZ (1.0 microg l(-1), 0.2 mg l(-1) and 2.0 mg l(-1)) for 42 days. Compared with the control, there was a significant lower (P < 0.05) condition factor in fish exposed at the highest concentration of CBZ (2.0 mg l(-1)), but the hepatosomatic indices in all groups were not significant changes. At lower CBZ concentration (1.0 microg l(-1), 0.2 mg l(-1)), the antioxidant enzyme activities were induced slightly, except catalase, while at the highest concentration (2.0 mg l(-1)) oxidative stress was apparent as reflected by the significant higher lipid peroxidation and protein carbonyls in the fish muscle, associated with a significant inhibition of antioxidant enzymes activities. Moreover, energy metabolic parameters (RNA-DNA ratio, Na(+)-K(+)-ATPase) were significantly inhibited in muscle of the fish exposed at the highest concentration (2.0 mg l(-1)), compared with the control. In short, CBZ-induced physiological and biochemical responses in fish were reflected in parameters measured in this study, which suggest that these biomarkers could be used as potential indicators for monitoring residual pharmaceuticals present in aquatic environment.
References provided by Crossref.org
Effects of mixture of pharmaceuticals on early life stages of tench (Tinca tinca)