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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.
Seminal plasma improves fertility of frozen equine semen.
Animal reproduction science    November 3, 2005   Volume 89, Issue 1-4 242-245 
Alghamdi AS, Madill S, Foster DN.No abstract available
Effects of hyaluronic acid supplementation on motility of stallion spermatozoa after cryopreservation.
Animal reproduction science    November 3, 2005   Volume 89, Issue 1-4 284-285 
Mari G, Iacono E, Rizzato G, Merlo B, Belluzzi S.No abstract available
Improvement of the freezability of sex-sorted stallion spermatozoa.
Animal reproduction science    November 3, 2005   Volume 89, Issue 1-4 315-318 
Buss H, Clulow J, Sieme H, Maxwell WM, Morris LH, Sieg B, Struckmann C, Rath D.No abstract available
Improvement of stallion semen post-thaw motility with the association dimethyl formamide and methyl formamide as cryoprotectors.
Animal reproduction science    November 3, 2005   Volume 89, Issue 1-4 286-288 
Carmo MT, Papa FO, Medeiros AS, Araujo GH, Alvarenga MA.No abstract available
Evaluation of a cushioned centrifugation technique for processing equine semen for freezing.
Animal reproduction science    November 3, 2005   Volume 89, Issue 1-4 245-248 
Ecot P, Decuadro-Hansen G, Delhomme G, Vidament M.No abstract available
Effects of beta-endorphin and naloxone on motility of cooled equine spermatozoa.
Animal reproduction science    November 3, 2005   Volume 89, Issue 1-4 223-225 
Mari G, Rizzato G, Iacono E, Merlo B, Minoia R, Belluzzi S.No abstract available
The effect of sodium hyaluronate on sperm function of cryopreserved equine spermatozoa.
Animal reproduction science    November 3, 2005   Volume 89, Issue 1-4 239-242 
Ottier DA, Curtis EF.No abstract available
Composition of fractionated stallion ejaculates.
Animal reproduction science    November 3, 2005   Volume 89, Issue 1-4 228-230 
Kareskoski AM, Reilas T, Sankari S, Andersson M, Katila T.No abstract available
Effects of cooling stallion semen for 24 h before freezing on fertility rates.
Animal reproduction science    November 3, 2005   Volume 89, Issue 1-4 250-252 
Melo CM, Zahn FS, Martin I, Alberti K, Orlandi C, Siqueira Filho ER, Dell'aqua JA, Alvarenga MA, Papa FO.No abstract available
The effect of sperm number and frequency of insemination on pregnancy rates of mares inseminated with frozen-thawed spermatozoa.
Animal reproduction science    November 2, 2005   Volume 89, Issue 1-4 203-205 
Barbacini S, Loomis P, Squires EL.No abstract available
Effects of frequency of insemination, number of spermatozoa and insemination site on fertility of equine frozen semen.
Animal reproduction science    November 2, 2005   Volume 89, Issue 1-4 208-211 
Clement F, Duchamp G, Larry JL, Vidament M.No abstract available
Influence of cryopreserved sperm or semen extender on uterine contractile activity in mares following conventional or hysteroscopic insemination.
Animal reproduction science    November 2, 2005   Volume 89, Issue 1-4 206-208 
Köllmann MC, Meinecke-Tillmann S, Swagemakers JH, Meinecke B.No abstract available
Influence of repeated treadmill exercise on quality and freezability of stallion semen.
Theriogenology    October 24, 2005   Volume 65, Issue 9 1737-1749 doi: 10.1016/j.theriogenology.2005.09.017
Janett F, Burkhardt C, Burger D, Imboden I, Hässig M, Thun R.The objective of this study was to investigate changes of quality and freezability of stallion semen in response to repeated acute treadmill exercise. Ejaculates from 11 stallions were collected, evaluated and frozen weekly during four periods of 4 weeks each defined as before (period 1), during (period 2) and after (periods 3 and 4) intense exercise. In fresh semen the gel-free volume, sperm concentration, motility, normal sperm and sperm with major defects (acrosome defects, nuclear vacuoles, abnormal heads, midpiece defects and proximal droplets) were evaluated. In frozen-thawed semen, moti...
Capacitation-like changes in equine spermatozoa following cryopreservation.
Theriogenology    October 12, 2005   Volume 65, Issue 8 1531-1550 doi: 10.1016/j.theriogenology.2005.08.022
Thomas AD, Meyers SA, Ball BA.The primary objective of this study was to assess plasma membrane characteristics and activation of signal transduction pathways in equine spermatozoa during both in vitro capacitation and cryopreservation. Significant plasma membrane restructuring, as assessed by measurement of plasma membrane lipid disorder and phospholipid scrambling, was not observed until after cryopreservation and subsequent thawing (P < 0.05). Although in vitro capacitated cells also displayed increased plasma membrane lipid disorder and phospholipid scrambling (P < 0.05), it appeared that regulation of these even...
Equine spermatozoal motility and fertility associated with the incorporation of d-(+)-mannose into semen extender.
Theriogenology    September 8, 2005   Volume 65, Issue 6 1171-1179 doi: 10.1016/j.theriogenology.2005.08.002
King SS, Speiser SA, Jones KL, Apgar GA, Wessels SE.Mannose is capable of decreasing bacterial attachment to the uterine mucosa in mares. Bacteria gain entry into the mare's uterus during breeding; therefore, a practical method to deliver mannose to the uterus is to incorporate it into semen extenders. The effect of mannose on spermatozoal motility and subsequent sperm fertilizing capability is unknown. The present study evaluated progressive spermatozoal motility in semen extender formulations incorporating mannose and assessed the fertility of mares inseminated with a mannose-containing semen extender. In Experiment 1, progressive spermatozoa...
The role of stallion seminal proteins in fertilisation.
Animal reproduction science    August 30, 2005   Volume 89, Issue 1-4 159-170 doi: 10.1016/j.anireprosci.2005.06.018
Töpfer-Petersen E, Ekhlasi-Hundrieser M, Kirchhoff C, Leeb T, Sieme H.Seminal plasma proteins are secretory proteins originating mainly from the epididymis and the accessory sex glands. They are involved in the remodelling of the sperm surface which occurs during sperm transit through the male genital tract and continues later at ejaculation. During this process, collectively called post-testicular sperm maturation, the spermatozoa acquire the ability to fertilise an egg. Seminal plasma proteins have been shown to contribute to early and central steps of the fertilisation sequence, e.g. the establishment of the oviductal sperm reservoir, modulation of capacitati...
Adding cholesterol to the stallion sperm plasma membrane improves cryosurvival.
Cryobiology    August 24, 2005   Volume 51, Issue 3 241-249 doi: 10.1016/j.cryobiol.2005.07.004
Moore AI, Squires EL, Graham JK.Cryopreservation induces partially irreversible damage to equine sperm membranes. Part of this damage occurs due to membrane alterations induced by the membrane changing from the fluid to the gel-state as the temperature is reduced lower than the membrane transition temperature. One way to prevent this damage is to increase the membrane fluidity at low temperatures by adding cholesterol to the membrane. Different concentrations of cholesterol-loaded-cyclodextrins (CLC) were added to stallion sperm to determine the CLC concentration that optimizes cryosurvival. Higher percentages of motile sper...
French field results (1985-2005) on factors affecting fertility of frozen stallion semen.
Animal reproduction science    August 23, 2005   Volume 89, Issue 1-4 115-136 doi: 10.1016/j.anireprosci.2005.07.003
Vidament M.Results on procedures for freezing stallion semen and the subsequent fertility during 20 years are presented. The present system applied in French National Stud includes: (1) a freezing protocol (dilution in milk, centrifugation and addition of freezing extender (INRA82+egg yolk (2%, v/v)+glycerol (2.5%, v/v) at 22 degrees C, a moderate cooling rate to 4 degrees C and freezing at -60 degrees C/min in 0.5-ml straws); (2) selection of ejaculates showing post-thaw rapid motility >35%; and (3) an insemination protocol (mares examined once daily, two AI of 400 x 10(6) spermatozoa 24 h apart before ...
Amides as cryoprotectants for freezing stallion semen: a review.
Animal reproduction science    August 16, 2005   Volume 89, Issue 1-4 105-113 doi: 10.1016/j.anireprosci.2005.07.001
Alvarenga MA, Papa FO, Landim-Alvarenga FC, Medeiros AS.Stallion semen cryopreservation, despite its impact on the horse industry, is not an established technology. During the last years, a number of modifications have been proposed to the freezing process, however, a large population of stallions still have poor semen quality and fertility after frozen-thawed. Glycerol toxicity could be a reason for the variation on stallion sperm freezability. There are limited publications concerning the use of alternative cryoprotectants for equine sperm. Glycerol is contraceptive for some species and other cryoprotectors, such as amides, have been show to be a...
Equine blastocyst development after intracytoplasmic injection of sperm subjected to two freeze-thaw cycles.
Theriogenology    August 10, 2005   Volume 65, Issue 4 808-819 doi: 10.1016/j.theriogenology.2005.04.035
Choi YH, Love CC, Varner DD, Hinrichs K.This study was conducted to evaluate the effects of thawing, division into aliquots and refreezing on fertilizing capacity (ability to support embryo development after intracytoplasmic sperm injection; ICSI) of frozen stallion semen. Frozen semen from a fertile stallion was thawed, diluted 1:100 with freezing extender, and refrozen (2F treatment). Control semen was frozen only once. In vitro matured equine oocytes were injected with: (1) motile control spermatozoa; (2) motile 2F spermatozoa; (3) non-motile 2F spermatozoa; or (4) non-motile 2F spermatozoa, followed by injection of sperm extract...
Integration of future biotechnologies into the equine industry.
Animal reproduction science    August 9, 2005   Volume 89, Issue 1-4 187-198 doi: 10.1016/j.anireprosci.2005.06.022
Squires EL.There has and will continue to be reproductive techniques available that have a positive impact upon the equine breeding industry. This review focuses on semen technologies that have been developed or are in the process of being developed. The use of fluorescent dyes and flow cytometry has provided the researcher and clinician with powerful tools to evaluate several sperm attributes. These procedures have been utilized to evaluate sperm viability, acrosome status, mitochondrial status, DNA integrity and stages of capacitation. Flow cytometry allows several sperm attributes to be evaluated on t...
Factors affecting the plasma membrane function of cooled-stored stallion spermatozoa.
Animal reproduction science    August 6, 2005   Volume 89, Issue 1-4 65-75 doi: 10.1016/j.anireprosci.2005.06.025
Aurich C.The spermatozoon is a highly specified cell that has the abilities of active motility and fertilization of the ovum. Damage to the sperm plasma membrane results in the irreversible loss of its functions. Because of the high content of unsaturated fatty acids in the plasma membrane, mammalian sperm are sensitive to oxidative stress. While mild peroxidation appears to promote capacitation of the sperm cell, excessive peroxidation will damage the plasma membrane and results in loss of motility and fertility. The functional integrity of the sperm plasma membrane can be determined by functional tes...
Effect of the inseminate and the site of insemination on the uterus and pregnancy rates of mares.
Animal reproduction science    August 3, 2005   Volume 89, Issue 1-4 31-38 doi: 10.1016/j.anireprosci.2005.06.023
Katila T.In this review, effects of the composition of the inseminate on uterine response and pregnancy rates in mares are discussed. The inseminate can differ for volume, sperm concentration, total sperm numbers, presence, absence, or proportion of seminal plasma, and extender composition. Semen can be used as fresh, cooled, or frozen. The site of semen deposition also plays a role; semen is deposited either into the uterine body (standard artificial insemination (AI)) or into the tip of the uterine horn ipsilateral to the preovulatory follicle (deep AI) using the hysterocopical or transrectally guide...
The development and application of the modern reproductive technologies to horse breeding.
Reproduction in domestic animals = Zuchthygiene    July 13, 2005   Volume 40, Issue 4 310-329 doi: 10.1111/j.1439-0531.2005.00602.x
Allen WR.Although the horse was probably the first animal to experience and benefit from artificial insemination, it trailed the field somewhat with regard to the application of embryo transfer and other oocyte and embryo-related modern breeding technologies. But with a late run it is now back in mid-field and gaining fast on the other large domestic species in the application of the many technological advances of the past 20 years to sound breeding practice. Improvements in extenders and cryoprotectants have resulted in a veritable upsurge in the transport and insemination of cooled and frozen stallio...
Characterization of an A-kinase anchor protein in equine spermatozoa and examination of the effect of semen cooling and cryopreservation on the binding of that protein to the regulatory subunit of protein kinase-A.
American journal of veterinary research    July 13, 2005   Volume 66, Issue 6 1056-1064 doi: 10.2460/ajvr.2005.66.1056
Turner RM, Casas-Dolz R, Schlingmann KL, Hameed S.To determine whether a homologue of A-kinase anchor protein 4 (AKAP4) is present and functional as an AKAP in equine spermatozoa and examine the effect of semen cooling and cryopreservation on binding of equine AKAP4 to the regulatory (RII) subunit of protein kinase-A (PK-A). Methods: Ejaculated semen collected from 2 fertile stallions, 3 bulls, and 3 humans. Methods: Identification of an equine homologue of AKAP4 was investigated via DNA sequencing. Protein was extracted from the spermatozoa of each species for immunoblot analysis to identify AKAP4 and its precursor protein, pro-AKAP4; immuno...
Low-dose insemination–why, when and how.
Theriogenology    July 12, 2005   Volume 64, Issue 3 572-579 doi: 10.1016/j.theriogenology.2005.05.012
Lyle SK, Ferrer MS.The typical dose for insemination into the uterine body of the mare is > 300 x 10(6) progressively motile spermatozoa (PMS) and an insemination dose of > 200 x 10(6) PMS is recommended for frozen-thawed semen. Low-dose insemination techniques allow for a drastic reduction in the numbers of spermatozoa required to achieve pregnancy. Acceptable pregnancy rates can be achieved with doses ranging from 1 to 25 x 10(6) PMS in volumes ranging from 20 to 1000 microL. Two techniques have been described: hysteroscopic insemination and transrectally guided deep horn insemination using a pipette. Similar ...
Effect of caspase inhibitors on the post-thaw motility, and integrity of acrosome and plasma membrane of cryopreserved equine spermatozoa.
Indian journal of experimental biology    July 5, 2005   Volume 43, Issue 6 483-487 
Peter AT, Colenbrander B, Gadella BM.The present study was designed to test the hypothesis that addition of anticaspase cocktails (inhibiting caspases and thus blocking apoptosis) to the extenders increases the post-thaw viability of equine spermatozoa. The addition of caspase inhibitors failed to improve the acrosome and plasma membrane integrity of spermatozoa, suggesting that in equine sperm cryopreservation protocols, the addition of these caspase inhibitors to cryopreservation medium may not be beneficial in protecting the sperm from the stress of cryopreservation.
Frozen semen management in equine breeding programs.
Theriogenology    June 22, 2005   Volume 64, Issue 3 480-491 doi: 10.1016/j.theriogenology.2005.05.028
Loomis PR, Squires EL.Success with frozen semen requires attention to detail and a basic understanding of the techniques for properly handling and thawing and inseminating frozen semen. Practitioners should also be familiar with strategies used for managing mares for insemination with thawed semen. This manuscript will review those techniques and also present fertility data collected in a commercial setting. Factors that affect pregnancy rates for mares inseminated with frozen-thawed semen such as timing and frequency of insemination were examined for two separate data sets consisting of 332 and 536 mare cycles col...
Influence of vedaprofen (Quadrisol) on quality and freezability of stallion semen.
Theriogenology    June 13, 2005   Volume 64, Issue 8 1867-1877 doi: 10.1016/j.theriogenology.2005.04.013
Janett F, Aebi L, Burger D, Imboden I, Hässig M, Kindahl H, Thun R.The objective of this study was to evaluate the effect of the non-steroidal anti-inflammatory drug (NSAID) vedaprofen (Quadrisol) on quality and freezability of stallion semen. Experiments were performed using 22 Franches Montagnes stallions from the National Stud in Avenches (Switzerland) randomly divided into a control and test group. Vedaprofen was given orally to all stallions of the test group at the recommended therapeutic dose (initial dose of 2mg/kg followed by 1mg/kg body weight every 12h) for 14 days. Control animals received the same amount of carrier substance. During treatment, bl...
Lipid peroxide formation in relation to membrane stability of fresh and frozen thawed stallion spermatozoa.
Molecular reproduction and development    June 11, 2005   Volume 72, Issue 2 230-238 doi: 10.1002/mrd.20322
Neild DM, Brouwers JF, Colenbrander B, Agüero A, Gadella BM.In this study we used a new method to detect reactive oxygen species (ROS) induced damage at the level of the sperm plasma membrane in fresh and frozen-thawed stallion sperm. Lipid peroxidation (LPO) in sperm cells was assessed by a fluorescent assay involving the labeling of stallion sperm with the LPO reporter probe C11-BODIPY(581/591). The peroxidation dependent spectral emission shift of this membrane probe could be localized using inverted spectral confocal microscopy and quantified on living and deteriorated sperm cells using flow cytometry. Mass spectrometric analysis of the main endoge...
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