The objective of this trial was to evaluate the efficiency of dimethylformamide on cryopreservation of goat semen using semen physical analyses and complementary tests. Alpine and Saanen bucks from the Dairy Goat Experimental Station- DZO were used. Semen samples were frozen with a yolk-skimmed milk diluent and cryoprotectors with different concentrations as follows: 7% glycerol (T1), 3.5% glycerol plus 3.5% dimethylformamide (T2) or 5% dimethylformamide (T3). Semen was centrifuged, diluted, and bottled in 0.5 mL straws followed by cooling for 40 minutes until reach 5.0°C and kept at this temperature for additional 80 minutes. Samples were then exposed to liquid nitrogen vapor for 15 minutes and finally frozen. Thawing was done in a waterbath at 37°C for 50 seconds. The following variables were evaluated in vitro: sperm progressive motility and vigor, acrosomal integrity and reaction, and plasmatic membrane integrity. The cryopreservation procedures reduced 30.0% of the initial motility and 19% of plasmatic membrane integrity that was evaluated using the hyposmotic swelling test (HOST). It was observed an increaseof 3% in acrosomal lesions when samples were submitted to a slow thermoresistance test (TRT). No significant differences in sperm motility were observed among treatments at 0, 5, and 60 minutes of TRT as well as in sperm vigor at all TRT times. However, at 120 minutes of TRT a significant difference in sperm motility was found comparing T1 and T2 while T3 was intermediate. There were no significant differences on plasmatic membrane integrity, acrosomal integrity, and post-thawing acrossomal reaction across treatments. It can be concluded that dimethylformamide can be a viable alternative for goat semen cryopreservation used alone or in association with glycerol.
glycerol; dimethyl formamide; goat semen
