Aj. Dhami et al., EFFECTS OF DIFFERENT VARIABLES ON THE FREEZABILITY, POSTTHAW LONGEVITY AND FERTILITY OF BUFFALO SPERMATOZOA IN THE TROPICS, Theriogenology, 46(1), 1996, pp. 109-120
A factorial experiment was conducted to determine the relative efficac
y of 2 diluents (Tris and milk), 4 cooling rates (10/30 degrees C to 5
degrees C; 1 and 2 h each), 2 equilibration periods at 5 degrees C (0
and 2 h), 3 thawing rates (4 degrees C/5 min, 40 degrees C/1 min and
60 degrees C/15 sec), and their interactions in the cryopreservation o
f Murrah buffalo (n=3) semen on the basis of pre- and post-freezing mo
tility, and post-thaw incubation (0, 30, and 60 min at 37 degrees C) a
nd aging (6, 24 and 48 h at 5 degrees C) motility, and fertility to fi
rst AI (806). The pre-freeze sperm motility was significantly lower (P
<0.05) following 1 and 2 h of direct cooling from 10 to 5 degrees C (6
5 and 70%) than the corresponding values of routine cooling from 30 to
5 degrees C (72 and 76%). Post-thaw forwardly motile spermatozoa at a
ll intervals of incubation or aging including conception rates (65.4 a
nd 68.1%; 90-d palpation confirmation) were significantly (P<0.01) hig
her following 2 h of prefreeze cooling both from 10 and 30 degrees C c
ompared with 1 h of cooling from the respective temperatures (59.5 and
63.4%). Further, 2 h of equilibration at 5 degrees C compared with 0
h significantly improved the post-thaw recovery (48 vs 39%), incubatio
n/aging survival (8 to 12%) and fertility rates (71 vs 56.5%) of froze
n semen. Post-thaw recovery and incubation/aging survival of buffalo s
permatozoa also increased significantly with each increment in thawing
temperature from 4 to 40 to 60 degrees C. There were positive correla
tions between post-thaw motility and longevity of spermatozoa, and fer
tility. Overall, both Tris- and milk-based diluents were equally effic
acious; slow cooling of straws from 30 to 5 degrees C for 2 h compared
with faster cooling (1 h) or lower initial temperature (10 degrees C)
and 2 h of equilibration at 5 degrees C appeared inevitable for succe
ssful cryopreservation of buffalo semen. A thaw rate of 60 degrees/15
sec yielded better post-thaw recovery and longevity and could improve
fertility of buffalo spermatozoa.