1Division of Animal and Fisheries Science, ICAR-Research Complex for NEH Region, Umiam-793 103, Meghalaya, India
2Department of Animal Reproduction, Gynaecology and Obstetrics, College of Veterinary Science, Assam Agricultural University, Khanapara, Guwahati-781 022, Assam, India
3Department of Mathematical Science, Gauhati University, Guwahati-781 022, Assam, India
*Corresponding Author: Himsikha Chakravarty, Division of Animal and Fisheries Science, ICAR Research Complex for NEH Region, Umiam-793 103, Meghalaya, India. Email: himsikhachakravarty@gmail.com
Online published on 17 March, 2023.
Goat semen has phospholipase A enzyme which makes removal of seminal plasma an important step in its preservation. This study was aimed to standardize a centrifugation regime for cryopreservation of Beetal buck semen.
A total of 36 pooled semen ejaculates were used for the experiment where initially 27 pooled ejaculates were utilized to find out the best time period out of 5, 8 and 11 minutes for each g-force viz., 700 × g, 1100 × g and 1400 × g using 9 pooled ejaculates per g-force. The remaining 9 pooled ejaculates were employed to find out the best centrifugation regime amongst the best time period for each g-force (8 minutes for 700 × g, 8 minutes for 1100 × g and 5 minutes for 1400 × g).
The percentage of sperm motility, live sperm, intact acrosome and HOST-reacted sperm differed significantly (P<0.0001) between time periods at 700 × g, 1100 × g and 1400 × g. The sperm parameters were significantly (P<0.05) higher at 1400 × g for 5 minutes and 1100 × g for 8 minutes than at 700 × g for 8 minutes. In conclusion, adoption of a high centrifugation force for a short duration of time for washing could improve the quality of frozen spermatozoa.
Beetal buck semen, Centrifugation regime, Cryopreservation, Intact acrosome
