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Background. Endocrine disrupting chemicals (EDCs), among them polychlorinated biphenyls (PCBs), are able to change the hormonal regulation of reproduction at the hypothalamo-pituitary-gonadal (HPG) axis in many vertebrates. The aim of the presently reported study was to determine the effects of highly chlorinated PCBs mixture—Delor 106—on the in vivo and in vitro luteinizing hormone (LH) secretion from the pituitary gland of female Prussian carp, Carassius gibelio (Bloch, 1782), at the time of natural spawning. Materials and Methods. In the in vivo experiment we tested exposure to Delor 106: acute (one week at the concentration of 700 ng · L–1) and chronic (5 weeks at increasing weekly concentrations, from 140 through 700 ng · L–1). Blood samples from all females were taken before intoxication (0 week) and subsequently every week (week 1 through 5) till the end of the experiment. In the in vitro experiment enzymatically dispersed pituitary cells obtained from sexually mature Prussian carp females were incubated for 5 or 24 h in the presence of Delor 106 at the concentrations of: 1, 5, 10, 50, or 100 ng · mL–1 of medium. LH levels in the incubation medium as well as in blood plasma were measured using ELISA method. Results. Long-term (3 and 4 weeks) exposure to the Delor 106, gradually added to the water, caused a significant elevation of spontaneous LH secretion. Pituitary cells incubation with Delor 106 at the concentration range from 10 through 100 ng · mL–1 of medium resulted in the significant increase of spontaneous LH secretion after 5 and 24 h. Conclusion. The results obtained in this study show that highly chlorinated biphenyl—Delor 106—changes the secretion of luteinizing hormone in Prussian carp in the spawning season, acting, at least in part, directly at the pituitary level.
The effects of naltrexone on the in vitro luteinizing hormone (LH) secretion from whole pituitary glands as well as from dispersed pituitary cells of common carp (Cyprinus carpio L.)in primary cell culture were studied. The perifusion of whole pituitary glands with naltrexone at a concentration of 10⁻⁴ M caused a significant increase of LH secretion compared to the control. This finding suggests that opioid peptides can indirectly affect LH secretion at the pituitary level, probably through the nerve terminals containing GnRH and/or DA present in the pituitary. In the perifusion of dispersed pituitary cells with naltrexone at concentrations of 10⁻⁶ or 10⁻⁴ M, significant increases of LH levels were found. Similar results were observed in static culture of dispersed carp pituitary cells: after 4 or 24 hours of culture in the medium containing naltrexone at concentrations of 10⁻⁶, 10⁻⁴ or 10⁻² M,a dose-dependent, statistically significant increase of LH secretion to the culture medium was found. The results from dispersed pituitary cell perifusions or cell culture with naltrexone indicate that this antagonist directly affects the pituitary cells and stimulates LH release from carp gonadotrophs.
The aim of this work was to evaluate the impact of different mercury concentrations (ranging from 0.05 to 1 ppm) on common carp sperm motility. Computer assisted sperm analysis (CASA) and microscopic observations of the time of sperm motility were applied in the experiment. According to analysis using the CASA method, it was found that all the tested concentrations of mercury decreased sperm motility, and that lethal effects were observed at concentrations of 0.5 and 1 ppm. On the other hand, microscopic observations showed that mercury decreased the time of sperm movement at doses as low as 0.2 ppm, and that lethal effects were evident at 1ppm. These results suggest the negative impact of mercury on sperm motility. The reasons for the differences in the results obtained using these two techniques are also discussed.
The effect of different cadmium concentrations on sperm motility in common carp was investigated. The motile activity of spermatozoa was evaluated by means of computer assisted sperm analysis (CASA) using three major parameters characterizing sperm movement - VCL, VAP and VSL. Moreover, subjective microscopic observations were performed in order to evaluate the average time of sperm movement. The following cadmium concentrations were tested: 10,50 100, 200, 500, 1.000 and 2.000 ppm. Computer assisted analysis and microscopic observations both showed that cadmium decreases the motility of carp spermatozoa in all tested concentrations, and that lethal effects were detectable at a concentration of 500 ppm (as determined by CASA) or 1.000 ppm (when manual microscopic observations were performed). Additionally, it was shown that low cadmium concentrations have the most negative influence on straight line velocity, which suggests the possible negative influence of cadmium on the ability of sperm to fertilize female gametes.
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