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Journal Article 2016; 37(Suppl 1): 60-66 PubMed PMID: 28263532 Citation  Keywords:  Animals, Carps:metabolism, Insecticides:toxicity, Pyrethrins:toxicity, Toxicity Tests:methods,.   

OBJECTIVES: The present study aimed to assess the acute effect of cypermethrin on common carp (Cyprinus carpio). Evaluation of toxicity effects of cypermethrin on carp was performed on based assessment of hematological profile, antioxidant and oxidative biomarkers and histopathology.

METHODS: For testing of toxicity was used the commercial product Cyperkill 25 EC - CY, which contains 250 g.L-1 of cypermethrin. Carp were exposed to two concentrations (1CY - 4.57 µg.L-1 and 2CY - 45.7 µg.L-1) of CY and a control for 96 hours.

RESULTS: Significant reduction (p<0.05) in leukocyte count were in fish exposed to concentration 45.7 µg.L-1 (2CY). The both exposure of CY lead to significant differences (p<0.01) in antioxidants biomarkers (superoxide dismutase, catalase, glutathione reductase, reduced glutathione and glutathione S-transferase) and in lipid peroxidation in carp tissues. Many of these changes were observed in liver, gills, muscle, intestine, brain and kidney. Additionally, exposure to CY caused many histological changes in gills, liver and caudal kidney.

CONCLUSION: Exposure to CY caused hematological, biochemical and histopathological changes in carp. This study provides and complements other important results for evaluating the toxicity effect of pyrethroids on fish.

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Journal Article 2014; 35(Suppl 2): 71-80 PubMed PMID: 25638369 Citation  Keywords:  Animals, Antioxidants:pharmacology, Carotenoids:pharmacology, Carps:metabolism, Chloramines:pharmacology, Diet, Oxidative Stress:drug effects, Sulfonamides:pharmacology, Tosyl Compounds:pharmacology,.   

OBJECTIVES: In fish aquaculture, disinfectants are used against bacterial and protozoal infections. These compounds cause oxidative stress that may stimulate the generation of reactive oxygen species, and subsequently the alteration in antioxidant systems of exposed organisms. Antioxidants like carotenoids present in microalgae increase carp resistance to oxidative stress after chemical treatment.

DESIGN: The aim of these experiments was to prove increased resistance of common carp (Cyprinus carpio L.) juveniles fed on experimental diets with microalgae biomass supplement (Algadiets) to oxidative stress caused by a disinfectant chloramine-T. In indoor experiments fish were fed on laboratory-prepared extruded diets containing supplement of Chlorella spp. (cf. C. vulgaris Beijerinck) biomass which contains antioxidants (carotenoids) like lutein. The young-of-the-year-old fish were acclimatized and fed on basal diet (control group) and the on diets containing 1, 2, 5 and 10% (w/w) of spray-dried Chlorella biomass (Algadiet 1, 2, 5 and 10) for 14 days followed by 6 weeks. Consequently, fish were treated daily with chloramine-T (Chl-T) at concentration of 10 mg x l(-1) for 1 h in three consecutive days. After this treatment, the indices of oxidative stress and antioxidant enzyme activity were assayed in fish gill, muscle and hepatopancreas.

RESULTS: The fish fed on different Algadiets had increased antioxidant enzyme activities of glutathione peroxidase, glutathione reductase and catalase in flesh after the exposure to Chl-T. Higher activities of superoxide dismutase, glutathione peroxidase and glutathione reductase were also observed in the hepatopancreas in all tested concentrations compared to the control group fed on the basal diet. The increased production and activity of antioxidant enzymes confirmed improved protection ability of fish tissues against oxidative damage when microalgae biomass was supplemented to the fish diet which was more pronounced by higher microalgae supplement in Algadiet 5 and 10 where the content of carotenoids was 105 mg and 214 mg per kilogram of fed, respectively.

CONCLUSION: The results show the positive effect of carotenoids from microalgae biomass to maintain the antioxidant capacity which increases resistance of fish to oxidative stress.

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Journal Article 2010; 31(Suppl 2): 105-113 PubMed PMID: 21187831 Citation  Keywords:  Animals, Carps:metabolism, Ceruloplasmin:metabolism, Cytochrome P-450 CYP1A1:metabolism, Cytochrome P-450 Enzyme System:metabolism, Dose-Response Relationship, Drug, Fungicides, Industrial:pharmacology, Gills:drug effects, Glutathione:metabolism, Glutathi.   

OBJECTIVES: The aim of the study was to investigate effects of the fungicide formulation Spartakus (prochloraz 450 g.L-1) on common carp Cyprinus carpio through biometric, biochemical, haematological and antioxidant indices, induction of xenobiotic metabolizing enzymes and histological examination of selected tissues.

DESIGN: The test was performed on juvenile fish, which was exposed to Spartakus (concentrations of prochloraz: 0.05; 0.15 and 0.38 mg.L-1) for 28 days. Haematological indices were assessed using unified methods of haematological examination in fish. Plasma biochemical indices were determined by biochemical analyzer. Concentration of total cytochrome P450 (CYP), glutathione (GSH) content and glutathione-S-transferase (GST) activity were determined spectrophotometrically in hepatopancreas. Activity of liver ethoxyresorufin-O-deethylase (EROD) activity was measured spectrofluorimetrically. Ferric reducing ability of plasma (FRAP) and ceruloplasmin activity were assessed spectrophotometrically. Histological changes in samples of hepatopancreas, skin, gills, spleen, head kidney and caudal kidney were examined by light microscopy.

RESULTS: There was a significant rise in hepatosomatic index (HSI) (p<0.01), CYP and EROD (p<0.05) of fish exposed to prochloraz of 0.15 and 0.38 mg.L-1 whereas GST was induced by all concentrations tested and GSH by 0.38 mg.L-1 (p<0.05). Red blood cell count decreased significantly (p<0.05) in prochloraz of 0.05 and 0.15 mg.L-1. Plasma potassium increased (p<0.01) in all Spartakus treated groups, a decline in total protein (p<0.05), ALT, Na+ and Ca (p<0.01) was found in fish exposed to prochloraz of 0.38 mg.L-1. Ceruloplasmin activity was elevated (p<0.05) in the highest concentration tested, FRAP declined (p<0.05) in the same group. Histopathological changes in gills were demonstrated in all pesticide treated groups, with a decreased activity of skin mucous cells in prochloraz of 0.38 mg.L-1.

CONCLUSION: The subchronic exposure to Spartakus influenced HSI, induced xenobitic metabolizing enzymes, initiated a disorder of selected plasma indices and a decline in red blood cell count, caused minor histological impairment, and affected antioxidant activities of the test fish....

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Journal Article 2010; 31(Suppl 2): 11-15 PubMed PMID: 21187820 Citation  Keywords:  Animals, Annexin A5:metabolism, Apoptosis:drug effects, Carps:metabolism, Caspases:metabolism, Cell Survival:drug effects, Dose-Response Relationship, Drug, Immune System:cytology, L-Lactate Dehydrogenase:metabolism, Lymphocytes:cytology, Models, Animal, .   

OBJECTIVES: The aim of this study was to assess the possible in vitro apoptotic effects of anatoxin-a on the selected immune cells isolated from the blood of carp.

DESIGN: In the experiments pure anatoxin-a was used at concentrations of 0.01, 0.05, 0.1 and 1 µg/ml RPMI-1640 medium. Apoptosis or necrosis of fish leukocytes (lymphocytes and phagocytes) induced by the toxin was determined by measurement of the activity of caspases-3/7 and the analysis of phosphatidylserine on the outer leaflet of apoptotic cell-membranes using Annexin-V-Fluorescein and Propidium Iodide. Moreover, fluorescent measurement of the release of lactate dehydrogenase from the cells with damaged membranes was done.

RESULTS: The viability of the lymphocytes exposed only to the highest concentration of anatoxin-a (1 µg/ml) was significantly decreased. The exposure to the toxin at higher concentrations (0.1 and 1 µg/ml) resulted in a significant increase of caspases 3/7 activity in phagocytes and lymphocytes. Moreover, fluorescent analysis with the use of annexin-V-fluorescein and propidium iodide staining showed more cells at the apoptotic stage than necrotic cells.

CONCLUSION: Our study showed that anatoxin-a is an inducer of apoptosis in fish immune cells....

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Comparative Study 2009; 30(1): 139-143 PubMed PMID: 19300396 Citation  Keywords:  Animals, Binding, Competitive, Carps:metabolism, Female, Gonadotropin-Releasing Hormone:metabolism, Humans, Mammals:metabolism, Pituitary Gland:metabolism, Protein Binding, Radioactive Tracers, Rats, Receptors, LHRH:metabolism, Salmon:metabolism,.   

OBJECTIVES: Receptor binding of GnRH is connected with the stimulation of pituitary gonadotropic cells leading to both the release and biosynthesis of gonadotropins. The binding is connected with the conformational changes in the receptor which induce the specific intracellular signalisation. The study of fish GnRHs and their receptors may give us new knowledge of the complex interplay of different mechanisms involved in neuroendocrine regulation of reproduction.

METHODS: Receptor binding of both mGnRH and sGnRH were compared by the study utilizing the displacement method with mGnRH or sGnRH as radioactive tracers. Incubation was performed at 2 degrees C to avoid ligand degradation.

RESULTS: The comparative binding of mGnRH and sGnRH with GnRH receptors from the female rat pituitary and female carp pituitary was studied. At the 50% of displacement, the binding of sGnRH to the rat pituitary receptor was very small and in comparison to the binding of mGnRH (100%) was in the range 2-15%. However, the binding of mGnRH to carp pituitary receptors is small in comparison with the binding of sGnRH (100%) and was in the range 5-20%.

CONCLUSION: The results demonstrated the differences in binding of different GnRHs to the receptor in rats and carp. This suggests that the structures of GnRH and its receptor undergo co-evolution in different classes of animals....

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Journal Article 2009; 30(Suppl 1): 230-235 PubMed PMID: 20027176 Citation  Keywords:  Aging, Animals, Biomarkers:blood, Carps:metabolism, Dose-Response Relationship, Drug, Herbicides:administration & dosage, Male, Random Allocation,.   

OBJECTIVES: We investigated the effects of the herbicide preparation Successor 600 on biochemical and haematological indices and the histolopathological parameters of common carp after 28 day exposure. Furthermore, the hepatosomatic index and induction of xenobiotic metabolizing enzymes and biomarkers were assessed.

DESIGN: Juvenile fish were exposed to sublethal concentrations of Successor(R) 600 (0.06 mg L-1, 0.22 mg L-1 or 0.60 mg L-1) for 28 days. Haematological indices were assessed using unified methods of haematological examination in fish. Plasma biochemical indices were measured by biochemical analyzer, the vitellogenin concentration in male fish plasma was estimated by direct sandwich ELISA. In hepatopancreas, ethoxyresorufin-O-deethylase (EROD) activity was measured spectrofluorimetrically, concentration of total cytochrome P450 (CYP), glutathion (GSH) content and glutathion-S-transferase (GST) activity were determined spectrophotometrically. Histological changes in samples of hepatopancreas, skin, gills, spleen, head kidney and trunk kidney were examined by light microscopy.

RESULTS: Haemoglobin, MCH and MCHC were significantly (p<0.05) reduced in fish treated with Successor(R) 600 of 0.22 and 0.60 mg L-1. LDH was enhanced (p<0.05), in the highest concentration of the preparation. Vitellogenin was detected in all male fish, with no difference between groups. HSI, GSH and GST were elevated (p<0.05), owing to the exposure, whereas CYP and EROD were not affected. Slight histopathological changes were demonstrated in skin, gills and hepatopancreas, with steroid tissue in head kidney samples of 0.60 mg L-1 treated fish.

CONCLUSION: Successor 600 affected the haematological profile of the treated fish, while the effects on biochemical indices were less expressed. Male plasma vitellogenin concentrations were not indicative of estrogen disruptive effects after 28 days. The importance of GSH and GST for the metabolisation were demonstrated. In contrast, CYP and EROD were not influenced by any concentration tested. HSI was found to reflex pollution with Successor 600. Histopathological indices caused by the treatment were observed in various tissue samples of the treated fish....

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