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The comparative study was performed on 200 European brown hares. Group I consisted of 35 clinically healthy hares kept in cages. Group II comprised 165 clinically healthy hares caught alive in their natural environment. Following the premedication, arterial and venous blood was drawn from the hares of the two groups studied. In the arterial blood, the acid-base balance (ABB) parameters were determined - blood pH, pCO₂, t CO₂, HCO₃⁻, BB, and BE. In the venous blood, the activity of AST, ALT, and FA, concentration of urea, creatinine, total protein, albumins, globulins, cholesterol, triglycerides, glucose, WBC, RBC, Hb, and Ht were determined. In addition, concentrations of Ca²⁺, P, Mg²⁺, Na⁺, K⁺, and Cl⁻ were measured in the blood serum. It was demonstrated that only the contents of globulins and triglycerides were similar in groups I and II. Concentration of electrolytes and ABB parameters were close to each other in the two studied groups, except for concentration of Mg²⁺ and inorganic P, and CO₂ molecular pressure. In the light of the obtained results a question remains opened: whether successful breeding, understood as an increase in the number of offspring of the reintroduced individuals, is more likely to occur in the case of animals caught alive and, adapted to living in their natural environment, or in the case of caged animals.
Testicular activity in brown hare Lepus europaeus Pallas, 1778 was studied during the annual cycle. Testicular mass, spermatozoa and testosterone were estimated. Percentages of haploid, diploid and tetraploid cells were monitored using DNA flow cytometry and the proportions of somatic and spermatogenetic cells were determined after selective labelling of somatic cells. Testis mass was high from January to July and declined thereafter to the nadir in September. Testis growth was reactivated signifi­cantly in December. Changes in testis mass corresponded with the spermatogenic efficacy (spermatozoa/g testis). High spermatogenic activity was characterized by intensive meiotic transformation of spermatocytes to spermatids, high percentages of haploid cells and low proportions of cells in the G2/M phase of mitosis. Proportions of haploid cells declined rapidly during the testis involution. Spermatogenesis was newly activated from November. The proportions as well as the ratios of spermatogenic and somatic cells differed significantly between the periods of testis involution and recru­descence, Testosterone level showed a pronounced increase in autumn preceding the intensification of spermatogenesis; the lowest concentration was found during prominent testis involution in August. The results suggest that the regulation of seasonal testicular activity is characterized by co-ordinated shifts in the relationships between mitosis, meiosis and testosterone production.
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