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Ecotoxicological impacts of clofibric acid and diclofenac in common carp (Cyprinus carpio) fingerlings: hematological, biochemical, ionoregulatory and enzymological responses. | LitMetric

AI Article Synopsis

  • The study examined the toxic effects of pharmaceutical drugs clofibric acid (CA) and diclofenac (DCF) on common carp (Cyprinus carpio) over 96 hours, focusing on various physiological parameters.
  • At all tested concentrations (1, 10, and 100 μg L(-1)), significant decreases were observed in red blood cells (RBC), plasma sodium, potassium, and glutamate oxaloacetate transaminase (GOT), while white blood cells (WBC), plasma glucose, protein, lactate dehydrogenase (LDH), and gill Na(+)/K(+)-ATPase levels increased.
  • The findings suggest that changes in hematological and biochemical parameters could serve as effective

Article Abstract

Investigation on the toxic effects of pharmaceutical drugs namely clofibric acid (CA) and diclofenac (DCF) were studied in a common carp Cyprinus carpio at different concentrations such as 1, 10 and 100 μg L(-1) for a short-term period of 96 h under static bioassay method. At all concentrations, red blood cell (RBC), plasma sodium (Na(+)), potassium (K(+)), and glutamate oxaloacetate transaminase (GOT) levels were decreased in fish treated with CA and DCF. Contrastingly, white blood cell (WBC), plasma glucose, protein, lactate dehydrogenase (LDH) and gill Na(+)/K(+)-ATPase level were increased. However, a mixed trend was observed in hemoglobin (Hb), hematocrit (Hct), plasma chloride (Cl(-)), mean cellular volume (MCV), mean cellular hemoglobin (MCH), mean cellular hemoglobin concentration (MCHC) and glutamate pyruvate transaminase (GPT) levels. There was a significant (P<0.01 and P<0.05) change in all parameters measured in fish exposed to different concentrations of CA and DCF. In summary, the alterations in hematological, biochemical, ionoregulatory and enzymological parameters can be used as biomarkers in monitoring the toxicity of CA and DCF in aquatic environment. However, more detailed studies on using of specific biomarkers to monitor the human pharmaceuticals are needed.

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Source
http://dx.doi.org/10.1016/j.jhazmat.2011.08.029DOI Listing

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