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Colloidal Centrifugation of Stallion Semen Results in a Reduced Rate of Sperm DNA Fragmentation
Author(s) -
Crespo F,
GutiérrezCepeda L,
Gosalvez J,
Serres C,
Johnston SD
Publication year - 2013
Publication title -
reproduction in domestic animals
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.546
H-Index - 66
eISSN - 1439-0531
pISSN - 0936-6768
DOI - 10.1111/j.1439-0531.2012.02140.x
Subject(s) - centrifugation , sperm , dna fragmentation , semen , andrology , biology , sperm motility , dna , incubation , fragmentation (computing) , microbiology and biotechnology , genetics , biochemistry , medicine , apoptosis , ecology , programmed cell death
Contents Stallion spermatozoa recovered and examined immediately after colloidal centrifugation resulted in a higher straight‐line velocity (VSL) than sperm processed using direct conventional centrifugation (p = 0.000), but there was no differences in the progressive motility or sperm DNA fragmentation (SDF) as determined by the sperm chromatin dispersion assay. However, when centrifuged spermatozoa were incubated at 37°C for 24 h to determine the rate of SDF (r‐SDF), a lower r‐SDF (p = 0.0011) was observed in those sperm recovered after colloidal separation (0.5 ± 0.1%/h) compared to direct (1.2 ± 0.4%/h) or no centrifugation (r‐SDF = 1.2 ± 0.3%/h). These results confirm that colloidal separation of stallion spermatozoa results in prolonged sperm DNA longevity, but these differences were only apparent following a period of incubation and dynamic assessment. Consequently, we strongly recommend the use of the dynamic form of the SDF assay for evaluating centrifugation and/or other ex vivo procedures, as a single basal assessment of SDF may inadvertently result in a false‐positive evaluation of DNA quality.