Twenty semen samples taken from 5 dogs were frozen in liquid nitrogen at 鈭?96 掳C in four different
extenders: one control
extender based on 20%egg yolk, 6%LDL alone (low density lipoproteins: the active cryoprotective principle in chicken egg yolk), 6%LDL combined with 20 mmol glutamine, and Equex庐 (a reference
extender that we wish to compare with the LDL-glutamine combination). After thawing, spermatozoal motility was evaluated using a HAMILTON THORNE CERROS 12 image analyzer; the percentage of motile spermatozoa was 27.7%in the egg yolk
extender (
p < 0.05), 49.9%with 6%LDL alone (
p > 0.05), 54.7%in the 6%LDL + 20 mmol glutamine
extender, and 47.9%with Equex庐 (
p > 0.05). The motility parameters (VAP, VCL, VSL and ALH) were also superior in the 6%LDL + 20 mmol glutamine
extender in comparison with the other
extenders.
Finally, the spermatozoa were generally better protected during freezing with the 6%LDL + 20 mmol glutamine association than with the egg yolk, 6%LDL, or Equex extenders in terms of the flagellar plasma membrane (HOS test), DNA (Acridine orange test), and acrosome integrity (Spermac庐 test: no significant difference). The Equex庐 extender obtained the best results for the acrosome, followed by 6%LDL + 20 mmol glutamine (FITC-PSA test: p < 0.05 between each extender).