Effects of single layer centrifugation (SLC) on bull spermatozoa prior to freezing on post-thaw semen characteristics.

Single layer centrifugation (SLC) has been shown to select the most robust spermatozoa from the ejaculate in several species. Here the effects of SLC prior to freezing on various parameters of frozen-thawed bovine sperm quality are reported. Semen from 8 bulls was layered on top of a species-specific colloid, Bovicoll. After centrifugation for 20 min at 300 g, the resulting sperm pellet was resuspended in OPTIXcell® (IMV Technologies, l'Aigle, France); the SLC-selected sperm samples and uncentrifuged controls were frozen. On thawing, all sperm samples were analysed for membrane integrity, production of reactive oxygen species, mitochondrial membrane potential (MMP) and chromatin integrity. The SLC-treated samples had a higher percentage of live, superoxide-positive spermatozoa than uncentrifuged samples (27.9 ± 5.1% versus 21.7 ± 6.7%; p = .03). They had a higher proportion of spermatozoa with high mitochondrial membrane potential than uncentrifuged samples (55.9 ± 8.2% versus 40.5 ± 15.1%; p = .03) and also a lower proportion of spermatozoa with low mitochondrial membrane potential than non-treated samples (42.0 ± 8.5% versus 55.9 ± 14.4%; p = .04). No significant effects of treatment were found for membrane integrity or chromatin integrity. The effect of bull was significant on the proportions of dead, superoxide-positive spermatozoa and live, hydrogen peroxide-negative spermatozoa, as well as on membrane integrity, but it was not significant for mitochondrial membrane potential or chromatin integrity. These results suggest that SLC selects the most metabolically active bull spermatozoa from the rest of the population in normal ejaculates; the pattern of reactive oxygen species production may be different in SLC-selected spermatozoa compared to unselected samples.

[1]  J. Morrell,et al.  Effect of Single Layer Centrifugation on reactive oxygen species and sperm mitochondrial membrane potential in cooled stallion semen. , 2017, Reproduction, fertility, and development.

[2]  J. Morrell,et al.  Effect of sperm preparation on development of bovine blastocyst in vitro , 2016, Zygote.

[3]  D. Evenson The Sperm Chromatin Structure Assay (SCSA(®)) and other sperm DNA fragmentation tests for evaluation of sperm nuclear DNA integrity as related to fertility. , 2016, Animal reproduction science.

[4]  A. Carluccio,et al.  Single and double layer centrifugation improve the quality of cryopreserved bovine sperm from poor quality ejaculates , 2016, Journal of Animal Science and Biotechnology.

[5]  M. Hoogewijs,et al.  Pregnancy rates after artificial insemination with cooled stallion spermatozoa either with or without single layer centrifugation. , 2014, Theriogenology.

[6]  J. Morrell,et al.  Quality of bull spermatozoa after preparation by single-layer centrifugation. , 2014, Journal of dairy science.

[7]  C. Vallorani,et al.  Effects of single layer centrifugation with Androcoll-P on boar sperm. , 2013, Animal reproduction science.

[8]  H. D. Guthrie,et al.  Effects of reactive oxygen species on sperm function. , 2012, Theriogenology.

[9]  M. Wallgren,et al.  Single Layer Centrifugation Can Be Scaled-Up Further to Process up to 150 mL Semen , 2012, ISRN veterinary science.

[10]  A. Boveris,et al.  Nitric oxide and superoxide anion production during heparin-induced capacitation in cryopreserved bovine spermatozoa. , 2011, Reproduction in domestic animals = Zuchthygiene.

[11]  H. Rodríguez-Martínez,et al.  Single layer centrifugation of stallion spermatozoa through Androcoll™-E does not adversely affect their capacitation-like status, as measured by CTC staining. , 2011, Reproduction in domestic animals = Zuchthygiene.

[12]  T. Khalifa,et al.  Sperm chromatin stability during in vitro manipulation of beef bull semen. , 2010, Reproduction in domestic animals = Zuchthygiene.

[13]  G. Evans,et al.  Pregnancy loss in heifers after artificial insemination with frozen-thawed, sex-sorted, re-frozen-thawed dairy bull sperm. , 2010, Animal reproduction science.

[14]  H. Rodríguez-Martínez,et al.  Colloidal centrifugation with Androcoll-E prolongs stallion sperm motility, viability and chromatin integrity. , 2009, Animal reproduction science.

[15]  H. Rodríguez-Martínez,et al.  Single-layer centrifugation with Androcoll-E can be scaled up to allow large volumes of stallion ejaculate to be processed easily. , 2009, Theriogenology.

[16]  H. Rodríguez-Martínez,et al.  In vitro fertilizing capacity of frozen-thawed bull spermatozoa selected by single-layer (glycidoxypropyltrimethoxysilane) silane-coated silica colloidal centrifugation. , 2009, Reproduction in domestic animals = Zuchthygiene.

[17]  H. Rodríguez-Martínez,et al.  Morphology and chromatin integrity of stallion spermatozoa prepared by density gradient and single layer centrifugation through silica colloids. , 2009, Reproduction in domestic animals = Zuchthygiene.

[18]  H. Rodríguez-Martínez,et al.  Biomimetic Techniques for Improving Sperm Quality in Animal Breeding: A Review , 2009 .

[19]  H. Bollwein,et al.  Interrelationship between plasma membrane integrity, mitochondrial membrane potential and DNA , 2008 .

[20]  H. Bollwein,et al.  Interrelationship between plasma membrane integrity, mitochondrial membrane potential and DNA fragmentation in cryopreserved bovine spermatozoa. , 2008, Reproduction in domestic animals = Zuchthygiene.

[21]  H. Rodríguez-Martínez,et al.  Prolongation of stallion sperm survival by centrifugation through coated silica colloids: a preliminary study , 2008 .

[22]  C. O’Flaherty,et al.  Sperm activation: role of reactive oxygen species and kinases. , 2008, Biochimica et biophysica acta.

[23]  D. Rath,et al.  Retained functional integrity of bull spermatozoa after double freezing and thawing using PureSperm density gradient centrifugation. , 2007, Reproduction in domestic animals = Zuchthygiene.

[24]  H. D. Guthrie,et al.  Determination of intracellular reactive oxygen species and high mitochondrial membrane potential in Percoll-treated viable boar sperm using fluorescence-activated flow cytometry. , 2006, Journal of animal science.

[25]  G. Evans,et al.  Assessment of in vitro sperm characteristics after flow cytometric sorting of frozen-thawed bull spermatozoa. , 2004, Theriogenology.

[26]  J. Thompson,et al.  Effect of storage time and temperature on stallion sperm DNA and fertility. , 2002, Theriogenology.

[27]  D. Evenson,et al.  Sperm chromatin structure assay: its clinical use for detecting sperm DNA fragmentation in male infertility and comparisons with other techniques. , 2002, Journal of andrology.

[28]  M. Diamond,et al.  Culture media and their components differ in their ability to scavenge reactive oxygen species in the plasmid relaxation assay. , 1999, Fertility and sterility.

[29]  D. Garner,et al.  Organelle‐specific probe JC‐1 identifies membrane potential differences in the mitochondrial function of bovine sperm , 1999, Molecular reproduction and development.

[30]  H. Rodríguez-Martínez,et al.  Evaluation of sperm damage and techniques for sperm clean-up. , 1997, Reproduction, fertility, and development.

[31]  C. Franceschi,et al.  A new method for the cytofluorimetric analysis of mitochondrial membrane potential using the J-aggregate forming lipophilic cation 5,5',6,6'-tetrachloro-1,1',3,3'-tetraethylbenzimidazolcarbocyanine iodide (JC-1). , 1993, Biochemical and biophysical research communications.

[32]  C. Thomas,et al.  Interrelationships among fluorometric analyses of spermatozoal function, classical semen quality parameters and the fertility of frozen-thawed bovine spermatozoa. , 1993, Theriogenology.