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Topic:Semen Preservation

Semen preservation involves the collection, processing, and storage of stallion semen for future use in artificial insemination. This practice enables the extension of genetic material across geographical boundaries and temporal constraints. The preservation process typically includes semen evaluation, dilution with extenders, cooling, and sometimes cryopreservation. Factors such as semen quality, extender composition, and storage conditions influence the success of preservation. This page compiles peer-reviewed research studies and scholarly articles that explore techniques, challenges, and advancements in the field of equine semen preservation, focusing on optimizing fertility outcomes and extending the reproductive lifespan of stallions.
Comparison of different extenders with defined protein composition for storage of stallion spermatozoa at 5 degrees C.
Reproduction in domestic animals = Zuchthygiene    July 20, 2007   Volume 42, Issue 4 445-448 doi: 10.1111/j.1439-0531.2006.00828.x
Aurich C, Seeber P, Müller-Schlösser F.To maintain the fertility of stallion spermatozoa during cooled storage, extender media are added to semen. In this study, three semen extenders were compared: EquiPro which contains defined caseinates and whey proteins instead of dried skim milk. The extender is provided in dry form and dissolved in distilled water prior to use. EquiPro TM has the same composition as EquiPro but is provided in a sterilized ready-to-use liquid form. AndroMed-E contains soybean lecithin as protein source. Semen was collected from seven stallions. Ejaculates were divided into three aliquots, diluted with the dif...
Influence of cryopreservation on mitochondrial functions in equine spermatozoa.
Theriogenology    July 17, 2007   Volume 68, Issue 5 745-754 doi: 10.1016/j.theriogenology.2007.06.004
Schober D, Aurich C, Nohl H, Gille L.Cryopreservation of spermatozoa is of essential importance for artificial insemination and breeding programs in horses. Besides other factors, spermatozoal motility depends on mitochondrial energy metabolism. Based on changes of single mitochondrial functions it has been suggested that mitochondrial damage during cryopreservation could be a major reason for diminished post thaw semen quality. However, it is still unclear to which extent this influences the whole bioenergetic performance of mitochondria and whether this plays a role during routine cryopreservation procedures. Therefore, it was ...
The costs of breed reconstruction from cryopreserved material in mammalian livestock species.
Genetics, selection, evolution : GSE    July 6, 2007   Volume 39, Issue 4 465-479 doi: 10.1186/1297-9686-39-4-465
Gandini G, Pizzi F, Stella A, Boettcher PJ.The aim of this work was to compare costs, in the horse, cattle, sheep, swine, and rabbit species, for the creation of gene banks for reconstruction of an extinct breed, using different strategies: embryos-only, embryos in combination with semen, and semen-only. Three cost measures were used: time required for population reconstruction, cost for creation of the gene bank, number of years-keeping-female to reach reconstruction. Semen costs were estimated across four scenarios: the presence or absence of a commercial market for semen, purchase of semen donors, and semen extracted from the epidid...
Ejaculate and type of freezing extender affect rates of fertilization of horse oocytes in vitro.
Theriogenology    July 5, 2007   Volume 68, Issue 4 560-566 doi: 10.1016/j.theriogenology.2007.04.057
Roasa LM, Choi YH, Love CC, Romo S, Varner DD, Hinrichs K.In vitro fertilization (IVF) was performed on in vitro-matured equine oocytes in three experiments. Frozen-thawed sperm were prepared using swim-up separation and heparin treatment. In Experiment 1, fertilization was achieved with sperm from only one frozen ejaculate of four obtained from the same stallion. Within this ejaculate, fertilization rates were higher with fresh media, as compared to media held for 6-8 days before use (39.6% versus 7.3%, respectively; P<0.001). The type of bovine serum albumin used affected fertilization rates (4% versus 39.6%; P<0.001). To determine if IVF rates wer...
Efficiency of short-term storage of equine semen in a simple-design cooling system.
Animal reproduction science    June 23, 2007   Volume 104, Issue 2-4 434-439 doi: 10.1016/j.anireprosci.2007.06.022
Nunes DB, Zorzatto JR, Costa e Silva EV, Zúccari CE.Five experiments tested the efficiency of a simple, low-cost system (CP) for cooling and storing equine semen at 2.0 degrees C for 24 h and 48 h. Pantaneiro stallions of known fertility were used. Semen quality was evaluated for progressive motility (PM), plasma membrane integrity (PMI), and pregnancy rate. Experiment 1 showed that PM and PMI were similar between CP and the control (Equitainer) in cooled semen. In Experiment 2, the influence was evaluated of combinations (four treatments) of two volumes (50/100 ml) and two sperm concentrations (500/750x10(6)) on sperm quality of semen cooled a...
A comparison of duck and chicken egg yolk for cryopreservation of stallion sperm.
Australian veterinary journal    June 6, 2007   Volume 85, Issue 6 232-235 doi: 10.1111/j.1751-0813.2007.00151.x
Clulow JR, Maxwell WM, Evans G, Morris LH.Duck and chicken egg yolk were compared for their protective effects against cold shock during the cryopreservation of stallion sperm in a lactose-EDTA-glycerol cryodiluent. Methods: A completely randomised design was used. Procedure Ejaculates from five stallions (n = 14 ejaculates) were split and diluted to either 20 or 200 x 10(6) sperm/mL in a lactose-EDTA extender containing either duck or chicken egg yolk. The extended semen was then frozen in liquid nitrogen. The percentage of sperm total motility and forward progressive motility were assessed before freezing and at 0 and 1 hr after tha...
In vitro development of equine oocytes from preserved ovaries after intracytoplasmic sperm injection.
The Journal of reproduction and development    May 17, 2007   Volume 53, Issue 4 877-885 doi: 10.1262/jrd.18167
Matsukawa K, Akagi S, Adachi N, Sato F, Hasegawa T, Takahashi S.In this study, we evaluated the meiotic competence of equine oocytes from ovaries preserved for one day. We also investigated fertilization, cleavage rate, developmental competence and freezability of equine embryos after intracytoplasmic sperm injection (ICSI). After collection from ovaries, the oocytes were classified into two groups comprised of those having compact cumulus layers (Cp) or those having expanded cumulus layers (Ex). Oocytes with a first polar body were subjected to fertilization by ICSI using frozen-thawed stallion spermatozoa and were then cultured in CR1aa medium. The rates...
Influence of bacteria and gentamicin on cooled-stored stallion spermatozoa.
Theriogenology    December 1, 2006   Volume 67, Issue 5 912-918 doi: 10.1016/j.theriogenology.2006.11.004
Aurich C, Spergser J.This study investigated effects of bacteria from the genital tract of horses and the effect of gentamicin in semen extender on spermatozoal function in cooled-stored stallion semen. Semen was collected from healthy stallions and processed with a milk-based extender with or without gentamicin (1g/l). Pseudomonas (Ps.) aeruginosa, Staphylococcus (St.) aureus, Streptococcus (Sc.) equi subsp. equi (Sc. equi), Sc. equi subsp. zooepidemicus (Sc. zooepidemicus), Sc. dysgalactiae subsp. equisimilis (Sc. equisimilis) or culture medium alone (control) were added. Immediately after addition of bacteria a...
Advanced methods for handling and preparation of stallion semen.
The Veterinary clinics of North America. Equine practice    November 30, 2006   Volume 22, Issue 3 663-676 doi: 10.1016/j.cveq.2006.07.002
Loomis PR.Clinical reproduction in the horse more closely parallels human clinical reproduction than in other domestic farm animals. Horse breeders rarely include fertility as a selection criterion when making mating decisions; in most breeds, there is no licensing or approval of stallions. This has led to a significant number of stallions in the breeding pool that possess desirable performance traits but are subfertile for a variety of reasons, some of them genetically transmitted between generations. Therefore, semen characteristics can vary greatly among stallions within the breeding population. A ch...
Viability and acrosome staining of stallion spermatozoa by Chicago sky blue and Giemsa.
Biotechnic & histochemistry : official publication of the Biological Stain Commission    November 30, 2006   Volume 81, Issue 4-6 109-117 doi: 10.1080/10520290600931007
Kútvölgyi G, Stefler J, Kovács A.A simple trypan blue-neutral red-Giemsa staining procedure for simultaneous evaluation of acrosome, sperm head, and tail membrane integrity and morphology has been used to evaluate equine spermatozoa. Some special characteristics and problems have arisen in evaluating stallion semen. One problem was the differentiation of intact vs. damaged sperm tails primarily in frozen and thawed samples. After freezing and thawing, a high percentage of spermatozoa with an unstained head and stained tail were observed. These cells are considered immotile. Therefore, unambiguous differentiation of intact vs....
Collection and freezing of epididymal stallion sperm.
The Veterinary clinics of North America. Equine practice    November 30, 2006   Volume 22, Issue 3 677-682 doi: 10.1016/j.cveq.2006.08.007
Bruemmer JE.The ability to harvest and preserve epididymal sperm from a stallion after simple elective castration, a catastrophic injury, or severe acute illness and subsequent death has been realized, allowing for the preservation of genetics that would have been lost otherwise.Currently, the care taken to collect the testes and epididymides properly, coupled with proper packaging and shipping, could make the greatest contribution to salvaging viable sperm. As advances in assisted reproductive techniques continue, more offspring may be obtained from stored epididymal sperm from valuable stallions.
Successful timing of ovulation using deslorelin (Ovuplant) is labour-saving in mares aimed for single ai with frozen semen.
Reproduction in domestic animals = Zuchthygiene    November 17, 2006   Volume 41, Issue 6 535-537 doi: 10.1111/j.1439-0531.2006.00709.x
Hemberg E, Lundeheim N, Einarsson S.To minimize the number of matings/inseminations, controlled ovulation has been practised since a long time ago. A potent short-term implant, releasing the GnRH analogue deslorelin (Ovuplant((R))) has been used in Australia and North America for several years for hastening the ovulation time in mares, but the product is not registered on the European market. This study was aimed to investigate: (1) ovulation time in mares implanted with Ovuplant when the largest follicle was 42 mm or more in size, (2) repeatability of ovulation time in successive oestruses when treated with Ovuplant, (3) pregna...
Anti-oxidative status and semen quality during cooled storage in stallions.
Journal of veterinary medicine. A, Physiology, pathology, clinical medicine    October 24, 2006   Volume 53, Issue 9 486-489 doi: 10.1111/j.1439-0442.2006.00879.x
Pagl R, Aurich C, Kankofer M.Activity of the anti-oxidative enzymes glutathione peroxidase (GSH-Px), superoxide dismutase (SOD) and catalase (CAT), content of thiobarbituric acid reactive substances (TBARS) and SH-groups were determined in native stallion semen (n = 8 stallions). Semen was then diluted in Kenney extender, EquiPro((R)) extender either with or without addition of N-acetyl cysteine or phosphate-buffered saline (PBS) and stored for 72 h at 5 degrees C. Correlations between initial activity of enzymes and development of semen motility and membrane integrity were calculated. Activities of GSH-Px, SOD and CAT im...
Effect of seminal plasma fractions on stallion sperm survival after cooled storage.
Journal of veterinary medicine. A, Physiology, pathology, clinical medicine    October 24, 2006   Volume 53, Issue 9 481-485 doi: 10.1111/j.1439-0442.2006.00882.x
Akcay E, Reilas T, Andersson M, Katila T.This study aimed to evaluate stallion sperm survival after 24 h of cooled storage in the presence of seminal plasma (SP) derived from the sperm-rich fractions (SRF) or sperm-poor fractions(SPF) of the ejaculate, without SP, or in the presence of SP from other stallions. Ejaculates were collected from four stallions using an automated phantom, which separated the semen into five cups. Centrifuged and washed spermatozoa from cup 2 (SRF) were mixed with skim milk extender to a concentration of 100 x 10(6) sperm/ml and then 1:1 (v/v) with SP from the stallion's own or another stallions' second (SP...
Post-testicular changes in the density and distribution of intramembrane particles of stallion sperm surface domains.
Animal reproduction science    October 2, 2006   Volume 100, Issue 1-2 204-210 doi: 10.1016/j.anireprosci.2006.08.027
López ML, Olea N, Retamal CA.Freeze-fracture replicas of stallion spermatozoa, collected from the proximal caput, corpus and cauda epididymides regions, were analyzed by electron microscopy to explore the distribution and density of intramembrane particles (IMP). Conspicuous differences in density and arrangement of the IMP were observed in the different topographical domains of mature and immature spermatozoa. A reduction of IMP, especially remarkable in the post-acrosomal domain, was observed in mature epididymal spermatozoa when compared with samples collected from ductuli efferentes. Some structural species-specific d...
Fertility of frozen-thawed stallion semen cannot be predicted by the currently used laboratory methods.
Acta veterinaria Scandinavica    August 17, 2006   Volume 48, Issue 1 14 doi: 10.1186/1751-0147-48-14
Kuisma P, Andersson M, Koskinen E, Katila T.The aim of the project was to use current simple and practical laboratory tests and compare results with the foaling rates of mares inseminated with commercially produced frozen semen. In Exp. 1, semen was tested from 27 and in Exp. 2 from 23 stallions; 19 stallions participated in both experiments. The mean number of mares per stallion in both experiments was 37 (min. 7, max. 121). Sperm morphology was assessed and bacterial culture performed once per stallion. In Exp. 1, progressive motility after 0, 1, 2, 3, and 4 h of incubation using light microscopy, motility characteristics measured wit...
Cryopreservation of horse semen under laboratory and field conditions using a Stirling Cycle freezer.
Cryo letters    August 8, 2006   Volume 27, Issue 3 179-186 
Faszer K, Draper D, Green JE, Morris GJ, Grout BW.A Stirling Cycle freezer has been developed as an alternative to conventional liquid nitrogen controlled rate freezers. Horse semen samples were cooled in 0.25 ml straws and 15 ml bags in the Stirling Cycle freezer under laboratory conditions and as a portable device, powered from a car battery. For comparison, straws were frozen in a conventional liquid nitrogen controlled rate freezer. Upon thawing, motility and viability of samples frozen in the Stirling Cycle freezer were not significantly different when compared to samples frozen in the liquid nitrogen freezer. Unlike liquid nitrogen syst...
Insemination doses: how low can we go?
Theriogenology    June 5, 2006   Volume 66, Issue 3 543-550 doi: 10.1016/j.theriogenology.2006.04.026
Brinsko SP.This manuscript presents a brief historical review of investigations related to equine artificial insemination. The origin of recommended insemination doses for use fresh, cooled and frozen semen will be reviewed. Over 30 years ago, an insemination dose of 500 x 10(6) progressively motile sperm (PMS) was recommended to maximize pregnancy rates when mares were bred with fresh semen under less than ideal conditions. Since that time, 500 x 10(6) progressively motile sperm has been almost universally accepted as a standard insemination dose, regardless of a stallion's fertility or the refinements ...
Comparison of three containers used for the transport of cooled stallion semen.
Theriogenology    May 27, 2006   Volume 48, Issue 7 1085-1092 doi: 10.1016/s0093-691x(97)00341-5
Katila T, Combes GB, Varner DD, Blanchard TL.Three containers commonly used to transport cooled equine semen (Equitainer, ExpectaFoal and a Swedish-designed semen-transport container, previously called the Salsbro Box and now called Equine Express) were compared, using four ejaculates from each of three stallions. Each ejaculate was diluted to a spermatozoal concentration of 25 x 10(6)/ml with a nonfat dry milk-glucose extender containing amikacin sulfate (1 mg/ml) and potassium penicillin G (1000 units/ml). Extended semen was divided into three 40-ml aliquots for placement in each of the three semen-transport containers. The extended se...
Equine frozen semen: freezability and fertility field results.
Theriogenology    May 27, 2006   Volume 48, Issue 6 907-917 doi: 10.1016/s0093-691x(97)00319-1
Vidament M, Dupere AM, Julienne P, Evain A, Noue P, Palmer E.The freezability of stallion semen defined as the number of selected ejaculates/total number of ejaculates frozen from 161 different stallions was analyzed. Of the stallions, 19, 30, 27 and 24% had a freezability of 0%, 0 to 33%, 33 to 66%, over 66%, respectively In 85 different stallions, the correlation of freezability between first and second year was 0.60 (P < 0.001). The relationship between fertility with fresh and frozen semen and freezability was analyzed in 40 stallions whose freezability and fertility information was recorded during 5 years. There was a strong relationship between fe...
Effective removal of equine arteritis virus from stallion semen.
Equine veterinary journal    May 19, 2006   Volume 38, Issue 3 224-229 doi: 10.2746/042516406776866444
Morrell JM, Geraghty RM.A method of removing equine arteritis virus (EAV) from equine semen used for artificial insemination is urgently needed. Recent medical studies suggest that a double semen processing technique of density gradient centrifugation followed by a 'swim-up' can provide virus-free sperm preparations for assisted reproduction. Objective: To investigate the use of the double semen processing technique to obtain virus-free sperm preparations from stallion semen containing EAV. Methods: Aliquots of an ejaculate from an uninfected stallion were spiked with virus and processed by the double processing tech...
Comparison of an extender containing defined milk protein fractions with a skim milk-based extender for storage of equine semen at 5 degrees C.
Theriogenology    April 18, 2006   Volume 66, Issue 5 1115-1122 doi: 10.1016/j.theriogenology.2006.03.006
Pagl R, Aurich JE, Müller-Schlösser F, Kankofer M, Aurich C.A problem of semen extenders based on milk or egg yolk is the fact that these biological products consist of a variety of substances. Extenders containing only components with clearly protective effects on spermatozoa would thus be an advantage. In this study, we have compared the effects of an extender containing defined caseinates and whey proteins only (EquiPro, defined milk protein extender) with skim milk extender on equine spermatozoa during cooled storage. The defined milk protein extender was used with and without the antioxidant N-acetyl cysteine (NAC). In a second experiment, semen w...
Motility and plasma membrane integrity of spermatozoa in fractionated stallion ejaculates after storage.
Reproduction in domestic animals = Zuchthygiene    January 20, 2006   Volume 41, Issue 1 33-38 doi: 10.1111/j.1439-0531.2006.00647.x
Kareskoski AM, Reilas T, Andersson M, Katila T.With the aim of investigating properties of stallion seminal plasma to eventually improve semen-handling techniques, sperm motility and plasma membrane integrity were analysed in different fractions of the ejaculates after storage. Semen was collected using a computer-controlled automated phantom that separates the ejaculates into five successive cups. Samples containing seminal plasma and skim milk extender were compared with samples stored in skim milk extender after the removal of seminal plasma by centrifugation. Fractionated ejaculates were stored cooled for 24 h after dilution with exten...
Recovery of Swedish Equine arteritis viruses from semen by cell culture isolation and RNA transfection.
Journal of virological methods    November 16, 2005   Volume 133, Issue 1 48-52 doi: 10.1016/j.jviromet.2005.10.017
Mittelholzer C, Johansson I, Olsson AK, Ronéus M, Klingeborn B, Belák S.Recovery of infectious Equine arteritis virus (EAV) from the semen of persistently infected Swedish stallions was attempted by classical cell culture isolation and by transfection of extracted total RNA. Whereas virus from semen samples stored for several months at -20 degrees C or from extended semen could only be recovered by transfection of extracted RNA, isolation in cell culture was achieved readily with fresh, unextended semen stored at -70 degrees C or directly used after sampling. In parallel, the viruses were examined in the variable region of the large glycoprotein GP5 by nested RT-P...
Effect of insemination volume on uterine contractions and inflammatory response and on elimination of semen in the mare uterus-scintigraphic and ultrasonographic studies.
Journal of veterinary medicine. A, Physiology, pathology, clinical medicine    November 5, 2005   Volume 52, Issue 9 466-471 doi: 10.1111/j.1439-0442.2005.00757.x
Sinnemaa L, Järvimaa T, Lehmonen N, Mäkelä O, Reilas T, Sankari S, Katila T.The effect of artificial insemination (AI) volume on uterine contractility and inflammation and on elimination of semen in the reproductive tract of mares was examined for 4 h after AI using two methods, scintigraphy and ultrasonography. The same doses were used in both methods: 2 and 100 ml of skim milk-extended frozen semen. In the scintigraphic study, the number of reproductively normal mares was four per group and in the ultrasonographic study five per group. For scintigraphy, the semen was radiolabelled with technetium-99m. The static scintigrams were acquired immediately before and 30, 6...
Prepackaging of equine semen in goblets prior to cryopreservation.
Animal reproduction science    November 3, 2005   Volume 89, Issue 1-4 248-250 
Love CC, White RD, Varner DD.No abstract available
Evaluation of slow cooling after centrifugation and glycerol addition at 22 degrees C versus direct freezing of semen in stallions with good and poor sperm longevity.
Animal reproduction science    November 3, 2005   Volume 89, Issue 1-4 299-302 
Knop K, Hoffmann N, Rath D, Sieme H.No abstract available
Cryopreservation of stallion semen collected from good and poor freezers using a directional freezing device (Harmony CryoCare–Multi Thermal Gradient 516).
Animal reproduction science    November 3, 2005   Volume 89, Issue 1-4 291-294 
Zirkler H, Gerbes K, Klug E, Sieme H.No abstract available
Effect of extender and method of preservation on motility of cooled stallion spermatozoa.
Animal reproduction science    November 3, 2005   Volume 89, Issue 1-4 281-283 
Rota A, Magelli C, Impeduglia R, Panzani D, Camillo F.No abstract available
Effects of cushioned centrifugation technique on sperm recovery and sperm quality in stallions with good and poor semen freezability.
Animal reproduction science    November 3, 2005   Volume 89, Issue 1-4 294-297 
Knop K, Hoffmann N, Rath D, Sieme H.No abstract available
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