Abstract

The objective of this study was to design a protocol to separate spermatozoa from seminal plasma of raw llama semen without prior enzymatic treatment using a single-layer centrifugation with Androcoll-E™ (AE). Two experiments were performed: (a) samples were divided into three aliquots (1ml) that were deposited on the top of 4, 5 or 6ml of AE and were centrifuged at 800g for 20min and (b) samples were divided into two aliquots (1ml) that were deposited on the top of 4ml of AE and were centrifuged at 600g or 1,000g for 20min. Columns of 5 and 6ml of AE showed a total sperm motility (TM) significantly lower, while in the 4ml column, this parameter was not different from the TM of samples before the AE treatment. The percentage of spermatozoa with intact and functional membranes, normal morphology and intact acrosomes, as well as the percentages of sperm with highly condensed chromatin, was conserved (p˃.05) in the three column heights and in the two centrifugation speeds evaluated. In conclusion, the different column heights of AE (4, 5 and 6ml) and the different centrifugation speeds used (600, 800 and 1,000g) allow separating spermatozoa of raw llama semen without enzymatic treatment, preserving the evaluated sperm characteristics. However, of all the studied treatments, centrifugation in the 4ml column of AE at 800g would be the method of choice to process raw llama semen samples destined for reproductive biotechnologies.

Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call