Topic:Cryopreservation
Cryopreservation in horses involves the process of cooling and storing biological samples at very low temperatures to preserve their viability for future use. This technique is primarily applied to equine gametes, embryos, and genetic material, such as semen and oocytes. The process aims to halt all biological activity, thereby maintaining the integrity of the samples over extended periods. Cryopreservation is utilized in equine breeding programs to enhance genetic diversity, support conservation efforts, and facilitate international genetic exchange. This page compiles peer-reviewed research studies and scholarly articles that explore the methodologies, challenges, and applications of cryopreservation in equine reproduction and genetics.
The evaluation of stallion semen in aspects of fertility control and its use for artificial insemination. Choice of the best methods for semen examination is dictated by the purpose of the examination, whether it be to assess the fertility of an individual stallion or to evaluate individual semen samples for routine purposes. In the author's experience of examining stallion semen, emphasis should be placed upon morphological examination, sperm cinematography and survival tests in vitro. Special problems concerning examination of frozen semen are discussed and the ultrastructure of spermatozoa frozen in the presence and absence of glycerol is described.
Studies on the preservation of raw and frozen horse semen. Retention of high motility of horse spermatozoa preserved at 4 degrees C was improved by a semen extender. Raw semen preserved for 2 to 8 hr at 4 degrees C gave an average conception rate of 67-3% but preservation for 1 to 2 days gave an extremely low conception rate. The conception rate from deep-frozen semen during 8 years was 56-3%.
Effect of timing of insemination, numbers of spermatozoa and extender components on the pregnancy rate in mares inseminated with frozen stallion semen. Fertilization rate was highest in mares inseminated with frozen semen within 12 hr of ovulation. Foaling rate was improved (P less than 0-05) by increasing the number of motile spermatozoa inseminated from 40 X 10(6) to 80 X 10(6) but was not further improved by increasing the number to 160 X 10(6) or by increasing the frequency of insemination from once to twice daily. The fertilizing capacity of spermatozoa frozen in one of the hydrogen ion extenders studied was dependent upon relative osmotic pressure and method of freezing (ampoules or pellets). Adjusting glycerol concentration from 7% to ...
Effects of cryopreservation on the acrosomal status of stallion spermatozoa. The effects of cryopreservation on the acrosomal status of equine spermatozoa were investigated. Ejaculates (n=10) from six stallions were processed fresh, after cooled storage at 4-6 degrees C for 24 h in either a milk-based or lactose-EDTA freezing extender and after freeze-thawing in lactose-EDTA extender in liquid nitrogen at either 5 x 10(7) or 2 x 10(8) spermatozoa ml(-1). All samples were incubated in TALP-TEST for 2 h at 39 degrees C in 5% CO2. Subsamples were challenged with calcium ionophore A23187 for 10 min. The acrosomal status of the spermatozoa was evaluated by staining the sper...
L-carnitine added to post-thawed semen acts as an antioxidant and a stimulator of equine sperm metabolism. The objective of this study was to enhance the in vitro sperm quality and in vivo fertility of frozen-thawed equine semen by the addition of l-carnitine (LC) to post-thawed semen. Different concentrations of LC were added to thawed samples to obtain four treatments control and 0.5, 1 and 2 mM LC. In the in vitro experiments, sperm motility and kinematics, membrane integrity and intracellular calcium ion concentration ([Ca ] ) were investigated, and the antioxidant bioactivity of LC was assessed by measuring hydrogen peroxide and nitrite concentrations (NO ). The fertility rate was assessed v...