Two Protocols of Cryopreservation of Goat Semen with the Use of Computer-Assisted Semen Analysis System

Kozdrowski R., A. Dubiel, W. Bielas, M. Dzięcioł: Two Protocols of Cryopreservation of Goat Semen with the Use of Computer-Assisted Semen Analysis System.Acta Vet. Brno 2007, 76: 601-604. The objective of the study was a comparison of two protocols of goat semen cryopreservation with the use of computer-assisted semen analysis system. Twenty ejaculates obtained with electroejaculation method were assessed. Each ejaculate was divided in half and frozen according to two protocols. In protocol I semen was centrifuged in order to remove its plasma and diluted in Tris buffer extender containing glucose, citric acid and glycerol with 20% addition of egg yolk. Protocol II did not include removal of plasma and the extender contained 1.5% egg yolk. It was shown that the removal of semen plasma improved motility of goat spermatozoa following freezing/thawing with respect to the following motility indicators: motility, average path velocity, amplitude of lateral head displacement at p < 0.05, and straight velocity, straightness and linearity at p < 0.01. In conclusion, the removal of semen plasma through centrifugation improved motility properties of goat semen following the freezing/thawing procedure. Semen plasma, spermatozoa, motility, freezing, cryopreservation, CASA, semen evaluation Semen crypreservation causes ultrastructural, biochemical and functional damage of spermatozoa, resulting in their decreased motility and viability. A specific problem limiting post-freezing properties of goat semen is the presence in semen plasma of an enzyme derived from bulbo-urethral glands, coagulating egg yolk (egg yolk coagulating enzyme EYCE) (Leboeuf et al. 2000). EYCE has been characterized as phospholipase A which hydrolyses egg yolk lecithin to fatty acids and lisolecithin. Lisolecithin is toxic to goat spermatozoa. The toxic effect can be partly eliminated by the removal of semen plasma which results in an increased proportion of live and motile spermatozoa. Motility of spermatozoa is among the most important indicators in semen quality assessment. At present the objective assessment of motility of spermatozoa is possible due to computer analysis considering many motility properties (Verstegen et al. 2002; Klimowicz et al. 2005). The objective of this study was to compare motility properties of goat spermatozoa subjected to freezing/thawing with or without a prior removal of plasma, with the use of the computer-assisted semen analysis system (CASA). Materials and Methods Semen was collected from 4 fertile male goats (each male had produced offspring, French Alpine breed), 3 4 years old, from January to March with the electroejaculation method. The males were fed a diet composed of hay, carrot and oats and were prepared for the operation by 12-hour starvation and premedication with xylasin (Sedazin) at the dose of 1.5 mg/10 kg b.w. Semen was collected into glass containers with water coat at a temperature of 37 °C. Following collection, the ejaculate volume was measured. The percentage of motile spermatozoa was determined in a light microscope with a thermostable table of 37 °C, under × 200 magnification, and spermatozoa concentration was calculated in the Thom-Zeiss chamber. Ejaculates of a volume exceeding 1 ml, sperm motility > 80% and sperm concentration > 10 × 108/ml were ACTA VET. BRNO 2007, 76: 601-604; doi:10.2754/avb200776040601 Address for correspondence: Dr. R. Kozdrowski Department and Clinic of Reproduction, Ruminants Diseases and Animal Health Protection Wrocław University of Environmental and Life Sciences Plac Grundwaldzki 49, 50-366 Wrocław, Poland Phone: +48 71 3205 313 E-mail: [email protected] http://www.vfu.cz/acta-vet/actavet.htm qualified for freezing. Five ejaculates from each male were thus qualified. Each ejaculate was divided in two equal parts and frozen according to the methods described below. Two extenders used in Australia for semen cryopreservation were used for freezing. In protocol I, semen was diluted at 33 °C in a 1 : 4 ratio in a buffer of the following composition: Tris 274.1 mM, glucose 55.5 mM, citric acid 87.08 mM, and then centrifuged for 10 min at 1500 g in order to remove semen plasma. Following centrifugation and removal of supernatant, the sediment was suspended as 1 : 1 in an extender of the following composition: buffer 80 ml and egg yolk 20 ml. Thus diluted semen was cooled to 10 °C and then half of the calculated dose of an extender of the following composition: glycerol 8 ml, egg yolk 20 ml, buffer 72 ml was added. After 30 min the other half of the extender was added, to the final concentration of 60 × 106 spermatozoa in the volume of 0.25 ml. In protocol II, the semen was diluted at 33 °C with an extender of the following composition: 375 mM Tris, 41.625 mM glucose, 124.0 mM citric acid, 6% glycerol and 1.5% egg yolk, to the final concentration of 60 × 106 spermatozoa in the volume of 0.25 ml. This extender is recommended by Ritar and Salomon (1983) for use without prior plasma removal. In protocols I and II the semen was cooled to 5 °C during 120 min, packed in straws of 0.25 ml volume, placed horizontally 5 cm above the surface of liquid nitrogen for 10 min, and the straws were then plunged in liquid nitrogen. After 7 days the straws were thawed in a water bath of 40 °C during 30 s. Using the same methods that were applied to fresh semen, the percentage of motile spermatozoa was determined for freezing-thawing semen and the assessment of motility indicators was performed with the CASA system (HTM IVOS 12.2, Hamilton-Throne Biosciences MA, USA), coupled with phase-contrast microscope, video camera and computer which made it possible to register and analyse the data. Four μl of semen diluted × 40 with an extender of the following composition: Tris 274.1 mM, glucose 55.5 mM, citric acid 87.08 mM were placed in chamber 20 μm deep (Leja 4, Leja products B.V. Holland) on a thermo-stable plate heated to 37 °C. Prior to the analysis it was necessary to enter technical parameters enabling a correct identification of goat spermatozoa. The following motility indicators were measured: VAP (average path velocity) average velocity of the smoothed cell path (μm/s), VSL (straight velocity) average velocity measured for the movement along a straight line from beginning to end (μm/s), VCL (cell velocity) average velocity measured along the actual path of the spermatozoon (μm/s), ALH (amplitude of lateral head displacement) amplitude of head oscillation (μm), STR (straightness) straight line character of movement as a ratio of VSL/VAP (%), LIN (linearity) linearity of movement as a ratio VCL/VAP (%), MOT (motility) motile spermatozoa (%), PMOT (progressive motility) spermatozoa with progressive movement (%) i.e. with VAP of 75 μm/sec and STR of 80% and RAP (rapid) proportion of rapidly moving spermatozoa (%). Each time the semen sample was scanned in 5 automatically selected fields, and the mean values of the five fields were used for statistical analysis. Following analysis, digital video recording of the last field was examined in order to confirm that all the spermatozoa were identified and their movement correctly interpreted by the device. Static cells were marked on the screen with a large red dot, the trajectory of spermatozoa interpreted as abnormal was marked with purple, the trajectory of normally moving spermatozoa with green. The results were presented as mean ± standard deviation; statistical analysis was based on Student’s t-test at the significance level of p < 0.05 and p < 0.01.