EFFECT OF DIFFERENT DISACCHARIDES ON THE INTEGRITY AND FERTILISING ABILITY OF FREEZE-DRIED BOAR SPERMATOZOA: A PRELIMINARY STUDY

Freeze-drying spermatozoa is a developing technique that facilitates semen storage and transport. However, freeze-dried sperm exhibits impaired DNA integrity, which is associated with reduced fertilizing ability. Boar spermatozoa were freeze-dried in three different freeze-drying EDTA buffers with trehalose (75mM) and lactose (75mM) (EDTA-TL), (2) with sucrose (75mM) and lactose (75mM) (EDTA-SL) or just lactose (150mM) (EDTA-LL) using two freeze-drying protocols. In experiment 1 a one-step protocol was used and in experiment 2 a two-steps protocol was used. Spermatozoa were stored in1.5 mL cryotubes and 1.5 mL glass ampules at both 16 degrees C and 25 degrees C for 1 month. Successfully freeze-dried speiinatozoa were stained with acridine-orange to assess chromatin stability. Freeze-drying was most successful when the 2-step protocol was used (experiment 2). Chromatin stability was greater in samples stored in glass ampules compared to cryo tubes. Chromatin stability was also greater in samples freeze-dried in EDTA-LL compared to EDTA-SL or EDTA-TL buffers. Spermatozoa freeze-dried in EDTA-LL and stored for 14 and 28 days at either 16 degrees C or 25 degrees C were utilized for ICSI. Two pronuclear formation wasgreatest using spermatozoa stored at 25 degrees C (69.23%) and for 28 days (50%). Although 16 degrees C spermatozoa samples had better stable chromatin, 25 degrees C spermatozoa samples offered better two pronuclear formation results. In conclusion, boar spermatozoa freeze-dried using media containing disaccharides exhibit high chromatin stability and are able to fertilise oocytes following ICSI. Disaccharides may therefore advance the development of freeze-drying techniques for spermatozoa enabling ease of sperm storage and transportation.