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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.
Insemination results with slow-cooled stallion semen stored for approximately 40 hours.
Acta veterinaria Scandinavica    January 1, 1994   Volume 35, Issue 3 257-262 doi: 10.1186/BF03548330
Heiskanen ML, Huhtinen M, Pirhonen A, Mäenpää PH.Semen from 3 stallions was extended using 2 methods (Kenney extender and a modified Kenney extender), slowly cooled, and stored for 41 +/- 6 (s.d.) h before insemination. An insemination dose (40 ml) contained 1.5-2 billion spermatozoa. In the experiment, 26 mares were inseminated in 30 cycles. The pregnancy rate per cycle obtained with sperm stored in the Kenney extender was 87% (n = 15). When the semen was extended with the modified extender, centrifuged and stored, the pregnancy rate was 60% (n = 15). Inseminations were done every other day until ovulation was detected. If a mare ovulated m...
Post-thaw motility and longevity of motility of imipramine-induced ejaculates of pony stallions.
Theriogenology    January 1, 1994   Volume 42, Issue 3 475-481 doi: 10.1016/0093-691x(94)90685-c
McDonnell SM, Oristaglio Turner RM.Imipramine-induced ex copula ejaculates (11) and fractionated in copula ejaculates were collected from each of 5 pony stallions for freezing in 5-ml straws (6), using a modified Kenney glucose skim-milk extender (2). Initial post-thaw total and progressive motilities and daily post-thaw total and progressive motilities, as well as the number of days to reach 0 progressively motile spermatozoa, were also similar for the 2 methods of collection. The percentage of morphologically normal spermatozoa both before freezing and after thawing were also similar for in copula and ex copula ejaculates. Co...
Preservation of ejaculated and epididymal stallion spermatozoa by cooling and freezing.
Theriogenology    January 1, 1994   Volume 41, Issue 4 809-818 doi: 10.1016/0093-691x(94)90497-7
Braun J, Sakai M, Hochi S, Oguri N.The suitability of ejaculated and epididymal stallion spermatozoa for cooled storage (5 degrees C) and cryopreservation was examined in 5 ejaculates from each of 6 stallions and in spermatozoa recovered from the cauda epididymidis after castration of these stallions. The percentage of progressively motile spermatozoa, examined by subjective estimation (cooled samples) or by computerized analysis (frozen-thawed samples), was used as parameter. In ejaculated semen samples containing 5 and 25% seminal plasma in a skim milk glucose extender, the lower amount of seminal plasma supported spermatozoa...
Freezability and fertility results with uncentrifuged stallion semen.
Acta veterinaria Scandinavica    January 1, 1994   Volume 35, Issue 4 377-382 doi: 10.1186/BF03548311
Heiskanen ML, Hilden L, Hyyppä S, Kangasniemi A, Pirhonen A, Mäenpää PH.The first (1 to 3) sperm-rich fractions of the ejaculate were collected from 4 stallions using an open-ended vagina. The volume of the collected fractions was 12 +/- 8 ml with a density of 475 +/- 200 million spermatozoa/ml. Before freezing, the semen was diluted with a skim-milk based extender 1:1 to 1:8 (volume of semen: volume of extender), depending on the initial sperm concentration to achieve a final concentration of 100 million/ml. The total number of spermatozoa in an insemination dose ranged from 0.7 to 1 billion spermatozoa. Within 12 h after ovulation, 48 mares were inseminated in 7...
[Cryopreservation trial with semen of purebred Arabian and Haflinger stallions in the Turkish national stud in Karacabey].
DTW. Deutsche tierarztliche Wochenschrift    December 1, 1993   Volume 100, Issue 12 476-478 
Tekin N, Yurdaydin N, Klug E, Daskin A, Keskin O, Kücük H.Within a German-Turkish university partnership deep freezing preservation of stallion semen was performed as a part project of the cooperation contract. In this study a modification of the introduced Makrotüb method was used for semen freezing. The investigated characteristics of fresh semen of the Arab stallions were in the normal range cited in the international literature. However, the semen data obtained from the Haflinger stallions were markedly and partially significantly in lower range than measured for the Arab stallions. This may reflect an incomplete adaptation process of the import...
The effectiveness of gentamicin or polymyxin B for the control of bacterial growth in equine semen stored at 20 degrees C or 5 degrees C for up to forty-eight hours.
Canadian journal of veterinary research = Revue canadienne de recherche veterinaire    October 1, 1993   Volume 57, Issue 4 277-280 
Vaillancourt D, Guay P, Higgins R.Semen from three stallions was used to evaluate the effectiveness of two antibiotics added to semen extender for samples stored at 20 degrees C or 5 degrees C for up to 48 hours. Each ejaculate was divided into six different treatments: semen+extender (SE); SE+gentamicin (100 micrograms/mL); SE+polymyxin B (1000 units/mL); and each of the above treatments inoculated with Pseudomonas aeruginosa ATCC 27853. Sampling of diluted semen for bacteriological analysis was performed after 2, 8, 24 and 48 hours of preservation at either temperatures. The presence of nonspecific bacteria was noted after t...
Capacitation-like membrane changes and prolonged viability in vitro of equine spermatozoa cultured with uterine tube epithelial cells.
American journal of veterinary research    September 1, 1993   Volume 54, Issue 9 1505-1510 
Ellington JE, Ball BA, Blue BJ, Wilker CE.Reliable capacitation of equine spermatozoa has been a major obstacle in the development of equine in vitro fertilization. Experiments were done to compare in vitro capacitation of equine spermatozoa by use of heparin/caffeine, calcium ionophore, uterine tube epithelial cell (UTEC)-conditioned medium, and direct culturing of spermatozoa with UTEC (coculturing). Capacitation-like changes, as determined by chlortetracycline membrane staining patterns, developed with UTEC-conditioned medium and coculturing, equivalent to that with calcium ionophore. Both of these treatments induced more (P < 0.05...
Liquid storage and freezing of semen from New Forest and Welsh Pony stallions.
DTW. Deutsche tierarztliche Wochenschrift    March 1, 1993   Volume 100, Issue 3 125-126 
Wöckener A, Colenbrander B.Two experiments were conducted to examine the effects of liquid storage extender and of a modified freezing protocol on motility and morphology parameters of 3-year-old pony stallions. In experiment 1 ejaculates were diluted 1 + 1 (v+v) with glycine-egg-yolk extender (D11) or skim milk extender (SME), centrifuged, resuspended in the corresponding extender and kept at +5 degrees C. Concerning motion characteristics, both progressive motility and average path velocity of semen stored in SME was significantly superior to semen stored in D11 after 6, 18 and 42 hrs. However, over time of storage th...
Column separation of motile sperm from stallion semen.
Journal of andrology    March 1, 1993   Volume 14, Issue 2 142-148 
Casey PJ, Robertson KR, Liu IK, Espinoza SB, Drobnis EZ.Subfertility in stallions is common, and methodologies are needed to increase the fertility in these animals. In other species, removal of the dead sperm from semen increases the quality and fertility of semen. With horse semen we evaluated 48 combinations of column separation techniques using micro-spin chromatography columns. The greatest improvement in motility was observed with glass wool, whereas glass beads exhibited the greatest recovery of motile sperm. Although centrifugation time did not influence recovery rate or percent motility, a column length of 2 cm was superior for recovery of...
Lipids and calcium uptake of sperm in relation to cold shock and preservation: a review.
Reproduction, fertility, and development    January 1, 1993   Volume 5, Issue 6 639-658 doi: 10.1071/rd9930639
White IG.When sperm of the ram, bull, boar and stallion are cold-shocked by rapid cooling to near freezing point, motility and metabolic activity are irreversibly depressed and the acrosome and plasma membrane disrupted. Ram sperm become susceptible to cold shock in the proximal corpus region of the epididymis when the cytoplasmic droplet has moved backwards to the distal portion of the sperm midpiece. The membrane constituents phospholipids and cholesterol are important in cold shock which causes loss of lipid from sperm. The susceptibility of sperm to cold shock is linked with a high ratio of unsatur...
Semen collection techniques.
The Veterinary clinics of North America. Equine practice    April 1, 1992   Volume 8, Issue 1 111-128 doi: 10.1016/s0749-0739(17)30470-4
Love CC.Semen collection techniques in the stallion have evolved considerably over the last 70 to 80 years and are used today primarily for artificial insemination. Semen can be collected from stallions that are otherwise unable to breed, allowing continued use of valuable animals. There are many options for collection of semen from stallions that present with ejaculatory dysfunction (see the article by McDonnell elsewhere in this issue.) Although there are many advantages to the use of artificial breeding, the collector must understand each step of the collection procedure as well as stallion prefere...
Artificial insemination and preservation of semen.
The Veterinary clinics of North America. Equine practice    April 1, 1992   Volume 8, Issue 1 205-218 doi: 10.1016/s0749-0739(17)30476-5
Brinsko SP, Varner DD.Artificial insemination is an effective technique for improving utilization of stallions in breeding programs. When proper semen handling and insemination procedures are used, optimal pregnancy rates are attainable. When AI techniques are employed for mares and stallions with marginal fertility, pregnancy rates may be improved in comparison with natural mating. Preservation of stallion semen in the liquid or frozen state reduces the costs and potential health hazards incurred by transporting mares and provides easier access to genetic material that may otherwise be unavailable. Acceptable preg...
Artificial insemination in horses.
The Veterinary record    February 8, 1992   Volume 130, Issue 6 128 doi: 10.1136/vr.130.6.128-a
Newcombe JR.No abstract available
Interactions between sperm packaging, gas environment, temperature and diluent on fresh stallion sperm survival.
Acta veterinaria Scandinavica. Supplementum    January 1, 1992   Volume 88 97-110 
Magistrini M, Couty I, Palmer E.No abstract available
Influence of conservation method on the motility and morphology of stallion semen (an international project).
Acta veterinaria Scandinavica. Supplementum    January 1, 1992   Volume 88 153-162 
Parlevliet J, Malmgren L, Boyle M, Wöckener A, Bader H, Colenbrander B.No abstract available
The role of selected biochemical components of equine seminal plasma in determining suitability for deep-freezing.
Archivum veterinarium Polonicum    January 1, 1992   Volume 32, Issue 1-2 17-29 
Bittmar A, Kosiniak K.Experiments conducted on the freezability of 400 ejaculates collected from 64 stallions demonstrate the possibility of predicting the semen's ability to withstand the freezing/thawing process. If the sperm concentration, AspAT activity and total protein content in the seminal plasma of raw ejaculates are determined before freezing, the effects of freezing may be forecast in about 80% of the ejaculates.
Equine artificial insemination in Central and East Europe.
Acta veterinaria Scandinavica. Supplementum    January 1, 1992   Volume 88 111-115 
Tischner M.No abstract available
Cryopreservation of stallion spermatozoa.
Acta veterinaria Scandinavica. Supplementum    January 1, 1992   Volume 88 129-135 
Klug E, Röbbelen I, Kneissl S, Sieme H.No abstract available
Automated analysis of stallion semen post-thaw motility.
Acta veterinaria Scandinavica. Supplementum    January 1, 1992   Volume 88 137-152 
Palmer E, Magistrini M.No abstract available
Use of frozen stallion semen in Europe.
Acta veterinaria Scandinavica. Supplementum    January 1, 1992   Volume 88 123-127 
Håård M.No abstract available
Proceedings of the 1st European Symposium on Production, Evaluation and Preservation of Stallion Semen. Uppsala, Sweden, October 1-2, 1992.
Acta veterinaria Scandinavica. Supplementum    January 1, 1992   Volume 88 1-167 
No abstract available
Current practical use of a glasswool/Sephadex filtration technique of frozen stallion semen.
Acta veterinaria Scandinavica. Supplementum    January 1, 1992   Volume 88 67-70 
Hellander JC.No abstract available
Evaluation of the use of transported chilled stallion semen in Sweden, 1987-1991.
Acta veterinaria Scandinavica. Supplementum    January 1, 1992   Volume 88 117-120 
Hellander JC.No abstract available
Assessment of sperm cell membrane integrity in the horse.
Acta veterinaria Scandinavica. Supplementum    January 1, 1992   Volume 88 49-58 
Colenbrander B, Fazeli AR, van Buiten A, Parlevliet J, Gadella BM.No abstract available
Techniques for collection and storage of stallion semen with minimal secondary contamination.
Acta veterinaria Scandinavica. Supplementum    January 1, 1992   Volume 88 83-90 
Tischner M, Kosiniak K.No abstract available
Evaluation of cryopreserved semen: an alternative assay.
Acta veterinaria Scandinavica. Supplementum    January 1, 1992   Volume 88 59-65 
Samper JC.No abstract available
Extender and centrifugation effects on the motility patterns of slow-cooled stallion spermatozoa.
Journal of animal science    August 1, 1991   Volume 69, Issue 8 3308-3313 doi: 10.2527/1991.6983308x
Padilla AW, Foote RH.Slow-cooled stallion spermatozoa, with and without seminal plasma removed by centrifugation, were diluted in Kenney's extender (KE) containing nonfat dry skim milk with glucose and antibiotics or in KE supplemented by adding a modified high-potassium Tyrode's medium (KMT). Four ejaculates from each of four stallions were collected and divided factorially across these four treatments. Percentage of motile sperm, path velocity, and linearity immediately after treatment (0 h) and after storage at 4 degrees C for 24, 48, and 72 h were evaluated objectively by use of a HTM-2030 sperm motility analy...
Relationship between the fertility of fresh and frozen stallion semen and semen quality.
Journal of reproduction and fertility. Supplement    January 1, 1991   Volume 44 107-114 
Samper JC, Hellander JC, Crabo BG.Studies were designed to investigate whether sperm motility determined with a Hamilton-Thorn HTM-2000 motility analyzer (HTM), or the percentage of spermatozoa that passed through glass wool (GW), Sephadex (S), or glass wool/Sephadex (GWS) filters could be used to predict the fertilizing potential of fresh or frozen semen. In the fresh semen study, 10 randomly selected ejaculates from 4 stallions exclusively used for A.I. breeding were assayed during the season. The 521 mares used were inseminated with 500 x 10(6) motile spermatozoa after gynaecological examination every 2 days. In the frozen ...
Penetration of frozen-thawed, zona-free hamster oocytes by fresh and slow-cooled stallion spermatozoa.
Journal of reproduction and fertility. Supplement    January 1, 1991   Volume 44 207-212 
Padilla AW, Tobback C, Foote RH.A method for preparing stored unfrozen stallion spermatozoa for the zona-free hamster oocyte penetration test (HOPT) and a subsequent comparison of fresh and stored sperm by the HOPT were evaluated. In Experiment 1, sperm from 4 stallion ejaculates, cooled to 4 degrees C and stored for 24 h, were treated with 60, 90 and 120 microM of dilauroylphosphatidyl-choline (PC12) liposomes to initiate the acrosome reaction. The percentage of motile and acrosome-reacted (AR) sperm were recorded after 8, 15 and 30 min of incubation at 39 degrees C, by automated image analysis. Liposome concentration did n...
Use of concanavalin A for coating the membranes of stallion spermatozoa.
Journal of reproduction and fertility. Supplement    January 1, 1991   Volume 44 191-198 
Blanc G, Magistrini M, Palmer E.Semen from three ejaculates from each of 4 stallions was frozen in liquid nitrogen. Morphology was evaluated by coating the spermatozoa with fluorescein-labelled Concanavalin A (FITC-ConA2) and motility was measured by computer-assisted image analysis. Coating was performed at each step of the freezing procedure (dilution, cooling, addition of glycerol and freeze-thawing) and observations were made after each step, to evaluate changes, or after subsequent steps, to determine protection provided by the coating method. All the parameters showed progressive changes during the freezing procedure. ...
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