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Effect of seminal plasma on the acrosome status of cryopreserved stallion spermatozoa

Michaela Toni

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Abstract

Today breeding through artificial insemination (AI) with cryopreserved semen is frequently used in \nseveral domestic species, but its use is more problematic in horses, partly because of reduced sperm \nquality and partly because the timing of insemination relative to ovulation is more crucial for frozen \nsemen than for fresh. Therefore, improvements in the freezing technique are needed. In this study, \nthe effect of adding pooled seminal plasma (SP) from stallions with good freezability (Good freezer \nstallion; GF) and bad freezability (Bad freezer stallion; BF) to spermatozoa selected by single layer \ncentrifugation from GF or BF stallions prior to cryopreservation was investigated. Of particular \ninterest was whether SP can have a positive impact on sperm acrosome status, thereby enhancing \nfertility. \nFrozen semen from 12 stallions was available. Aliquots of 5 ml from each ejaculate through normal \ncentrifugation and then frozen were used as controls (C). The remaining parts of the ejaculates were \nprocessed by single layer centrifugation (SLC) to remove SP and divided into three aliquots; sample \nwithout SP addition (S), sample with SP from GF (S-GF) and sample with SP from BF (S-BF). After \nthawing, the proportion of live or dead spermatozoa in the sample and the proportion of spermatozoa \nwith an intact or reacted acrosome were evaluated by flow cytometry. \nThe results indicate that the source of the SP (GF or BF) and the origin of the spermatozoa (GF or \nBF) were important. There was a positive effect of adding SP from GF to SLC-selected spermatozoa \n(p = 0.0017) compared to the control sample. If the sperm samples were divided according to \nwhether they came from good freezer stallions or bad freezer stallions, the effect of adding SP was \nmost marked when the spermatozoa came from a BF stallion (P = 0.04). In other words, the effect \nof adding SP to sperm samples is due to both the SP and the spermatozoa themselves. No statistical \ndifferences were seen between the different treatments (S, S-GF and S-BF) of SLC-selected samples. \nTo draw more reliable conclusions more studies are needed. The study also confirms SLC as a \nreliable processing method for increasing sperm survival during freezing.

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What this paper is about

Today breeding through artificial insemination (AI) with cryopreserved semen is frequently used in \nseveral domestic species, but its use is more problematic in horses, partly because of reduced sperm \nquality and partly because the timing of insemination relative to ovulation is more crucial for frozen \nsemen than for fresh. Therefore, improvements in the freezing technique are needed. In this study, \nthe effect of adding pooled seminal plasma (SP) from stallions with good freezability (Good freezer \nstallion; GF) and bad freezability (Bad freezer stallion; BF) to spermatozoa selected by single layer \ncentrifugation from GF or BF stallions prior to cryopreservation was investigated. Of particular \ninterest was whether SP can have a positive impact on sperm acrosome status, thereby enhancing \nfertility. \nFrozen semen from 12 stallions was available. Aliquots of 5 ml from each ejaculate through normal \ncentrifugation and then frozen were used as controls (C). The remaining parts of the ejaculates were \nprocessed by single layer centrifugation (SLC) to remove SP and divided into three aliquots; sample \nwithout SP addition (S), sample with SP from GF (S-GF) and sample with SP from BF (S-BF). After \nthawing, the proportion of live or dead spermatozoa in the sample and the proportion of spermatozoa \nwith an intact or reacted acrosome were evaluated by flow cytometry. \nThe results indicate that the source of the SP (GF or BF) and the origin of the spermatozoa (GF or \nBF) were important. There was a positive effect of adding SP from GF to SLC-selected spermatozoa \n(p = 0.0017) compared to the control sample. If the sperm samples were divided according to \nwhether they came from good freezer stallions or bad freezer stallions, the effect of adding SP was \nmost marked when the spermatozoa came from a BF stallion (P = 0.04). In other words, the effect \nof adding SP to sperm samples is due to both the SP and the spermatozoa themselves. No statistical \ndifferences were seen between the different treatments (S, S-GF and S-BF) of SLC-selected samples. \nTo draw more reliable conclusions more studies are needed. The study also confirms SLC as a \nreliable processing method for increasing sperm survival during freezing.

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Available abstract

Today breeding through artificial insemination (AI) with cryopreserved semen is frequently used in \nseveral domestic species, but its use is more problematic in horses, partly because of reduced sperm \nquality and partly because the timing of insemination relative to ovulation is more crucial for frozen \nsemen than for fresh. Therefore, improvements in the freezing technique are needed. In this study, \nthe effect of adding pooled seminal plasma (SP) from stallions with good freezability (Good freezer \nstallion; GF) and bad freezability (Bad freezer stallion; BF) to spermatozoa selected by single layer \ncentrifugation from GF or BF stallions prior to cryopreservation was investigated. Of particular \ninterest was whether SP can have a positive impact on sperm acrosome status, thereby enhancing \nfertility. \nFrozen semen from 12 stallions was available. Aliquots of 5 ml from each ejaculate through normal \ncentrifugation and then frozen were used as controls (C). The remaining parts of the ejaculates were \nprocessed by single layer centrifugation (SLC) to remove SP and divided into three aliquots; sample \nwithout SP addition (S), sample with SP from GF (S-GF) and sample with SP from BF (S-BF). After \nthawing, the proportion of live or dead spermatozoa in the sample and the proportion of spermatozoa \nwith an intact or reacted acrosome were evaluated by flow cytometry. \nThe results indicate that the source of the SP (GF or BF) and the origin of the spermatozoa (GF or \nBF) were important. There was a positive effect of adding SP from GF to SLC-selected spermatozoa \n(p = 0.0017) compared to the control sample. If the sperm samples were divided according to \nwhether they came from good freezer stallions or bad freezer stallions, the effect of adding SP was \nmost marked when the spermatozoa came from a BF stallion (P = 0.04). In other words, the effect \nof adding SP to sperm samples is due to both the SP and the spermatozoa themselves. No statistical \ndifferences were seen between the different treatments (S, S-GF and S-BF) of SLC-selected samples. \nTo draw more reliable conclusions more studies are needed. The study also confirms SLC as a \nreliable processing method for increasing sperm survival during freezing.

Key concepts: Semen, Andrology, Cryopreservation, Artificial insemination, Sperm, Acrosome, Insemination, Centrifugation

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