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Topic:Sperm

Equine sperm refers to the male reproductive cells produced by stallions, essential for the process of fertilization and successful breeding in horses. The study of equine sperm encompasses various aspects, including morphology, motility, viability, and genetic integrity. These parameters are critical for assessing stallion fertility and improving breeding outcomes. Research in this field often focuses on understanding the factors that influence sperm quality, such as age, nutrition, and environmental conditions. Additionally, advancements in assisted reproductive technologies, such as artificial insemination and cryopreservation, rely heavily on the detailed study of sperm characteristics. This page compiles peer-reviewed research studies and scholarly articles that explore the biology, evaluation, and technological applications related to equine sperm.
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 sperm chromatin structure assay: a review of clinical applications.
Animal reproduction science    September 6, 2005   Volume 89, Issue 1-4 39-45 doi: 10.1016/j.anireprosci.2005.06.019
Love CC.The sperm chromatin structure assay (SCSA) was introduced by as a method to determine the susceptibility of sperm DNA to denaturation and how those results related to fertility. This initial study used human sperm and was followed by studies in bulls and boars . This assay was one of the first to introduce the technique of flow cytometry, which has the ability to evaluate specific sperm compartments of large numbers of sperm in a short time, as a methodology to evaluate sperm quality and further define the relationship of sperm quality to fertility. For any assay to be of use clinically, it mu...
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 ...
Components in seminal plasma regulating sperm transport and elimination.
Animal reproduction science    August 17, 2005   Volume 89, Issue 1-4 171-186 doi: 10.1016/j.anireprosci.2005.07.005
Troedsson MH, Desvousges A, Alghamdi AS, Dahms B, Dow CA, Hayna J, Valesco R, Collahan PT, Macpherson ML, Pozor M, Buhi WC.Seminal plasma has been suggested to be involved in sperm transport, and as a modulator of sperm-induced inflammation, which is thought to be an important part of sperm elimination from the female reproductive tract. This article reports on recent experiments on the importance of seminal plasma components in sperm transport and elimination. In Experiment 1, hysteroscopic insemination in the presence (n = 3) or absence (n = 3) of 2 ng/mL PGE showed an increased portion of spermatozoa crossing the utero-tubal junction in the presence of PGE in two mares, while no difference was observed between ...
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...
Challenges facing sex preselection of stallion spermatozoa.
Animal reproduction science    August 9, 2005   Volume 89, Issue 1-4 147-157 doi: 10.1016/j.anireprosci.2005.06.024
Morris LH.Since the production of the first live offspring from sex-sorted spermatozoa in 1989, there have been many developments in the fluorescence-activated cell separation (FACS) procedures to preselect X- and Y-chromosome bearing spermatozoa prior to insemination. During this time, FACS technology has been applied to a range of species and has resulted in offspring from rabbits, cattle, sheep, elk and horses. In horses, satisfactory fertility rates have been achieved after hysteroscopic insemination of 20 x 10(6) fresh or stored, sex-sorted spermatozoa. However, many of the sperm processing protoco...
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...
Genetic markers for stallion fertility–lessons from humans and mice.
Animal reproduction science    August 2, 2005   Volume 89, Issue 1-4 21-29 doi: 10.1016/j.anireprosci.2005.06.021
Leeb T, Sieme H, Töpfer-Petersen E.Our knowledge on the many aspects of mammalian reproduction in general and equine reproduction in particular has greatly increased during the last 15 years. Advances in the understanding of the physiology, cell biology, and biochemistry of reproduction have facilitated genetic analyses of fertility. Currently, there are more than 200 genes known that are involved in the production of fertile sperm cells. The completion of a number of mammalian genome projects will aid in the investigation of these genes in different species. Great progress has been made in the understanding of genetic aberrati...
Capacitation, acrosome function and chromatin structure in stallion sperm.
Animal reproduction science    August 2, 2005   Volume 89, Issue 1-4 47-56 doi: 10.1016/j.anireprosci.2005.06.017
Neild DN, Gadella BM, Agüero A, Stout TA, Colenbrander B.In general, fertility in breeding stallions is lower and more variable than in the other farm animal species, primarily because selection is based on pedigree, looks and/or athletic performance, with little consideration of fertility or fertility potential. Moreover, because the average stallion breeds only a limited number of mares per year and in-field fertility is influenced significantly by non-stallion factors such as management and mare fertility, meaningful fertility data are hard to come-by. Unfortunately, generating usable figures would involve impractically high costs, time and numbe...
Theriogenology question of the month. Urospermia.
Journal of the American Veterinary Medical Association    July 29, 2005   Volume 227, Issue 2 225-227 doi: 10.2460/javma.2005.227.225
Dascanio JJ, Witonsky SG.No abstract available
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.
Update on equine ICSI and cloning.
Theriogenology    June 30, 2005   Volume 64, Issue 3 535-541 doi: 10.1016/j.theriogenology.2005.05.010
Hinrichs K.Intracytoplasmic sperm injection (ICSI) has recently become efficient enough to be considered for clinical use. With ICSI, one spermatozoa is injected into a mature oocyte. Harvesting of an oocyte ex vivo, followed by ICSI and transfer of the fertilized oocyte to the oviduct, may be applicable when semen quality is insufficient for standard insemination. Sperm injection, followed by in vitro embryo culture to the blastocyst stage, may be used in cases where multiple oocytes are to be fertilized (e.g. when oocytes are collected post-mortem). Nuclear transfer (cloning) of horses is possible but ...
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...
Assessment of the cryopreservation of equine spermatozoa in the presence of enzyme scavengers and antioxidants.
American journal of veterinary research    June 7, 2005   Volume 66, Issue 5 772-779 doi: 10.2460/ajvr.2005.66.772
Baumber J, Ball BA, Linfor JJ.To evaluate the effect of the addition of enzyme scavengers and antioxidants to the cryopreservation extender on characteristics of equine spermatozoa after freezing and thawing. Methods: 2 ejaculates collected from each of 5 stallions. Methods: Equine spermatozoa were cryopreserved in freezing extender alone (control samples) or with the addition of catalase (200 U/mL), superoxide dismutase (200 U/mL), reduced glutathione (10 mM), ascorbic acid (10 mM), alpha-tocopherol (25, 50, 100, or 500 microM or 1 mM), or the vehicle for alpha-tocopherol (0.5% ethanol). After thawing, spermatozoal motili...
Effect of alpha-tocopherol and tocopherol succinate on lipid peroxidation in equine spermatozoa.
Animal reproduction science    May 25, 2005   Volume 87, Issue 3-4 321-337 doi: 10.1016/j.anireprosci.2004.12.004
Almeida J, Ball BA.The objective of this study was to compare the effect of alpha-tocopherol and its ester, alpha tocopherol succinate, on lipid peroxidation and motility of equine spermatozoa. In experiment one, spermatozoa were incubated with dl-alpha-tocopherol (5, 25, 100 or 500 microM), DL-alpha tocopherol succinate (5, 25, 100 or 500 microM) or vehicle (0.5% ethanol) at 38 degrees C, and sperm motility was determined at 30, 60 and 120 min. In experiment two, spermatozoa loaded with the lipophilic probe, C11BODIPY(581/591), were incubated with dl-alpha-tocopherol (50 and 100 microM), DL-alpha-tocopherol suc...
Effect of seminal plasma on the cryopreservation of equine spermatozoa.
Theriogenology    May 25, 2005   Volume 63, Issue 9 2372-2381 doi: 10.1016/j.theriogenology.2004.05.032
Moore AI, Squires EL, Graham JK.Seminal plasma is generally removed from equine spermatozoa prior to cryopreservation. Two experiments were designed to determine if adding seminal plasma back to spermatozoa, prior to cryopreservation, would benefit the spermatozoa. Experiment 1 determined if different concentrations of seminal plasma affected post-thaw sperm motility, viability and acrosomal integrity of frozen/thawed stallion spermatozoa. Semen was washed through 15% Percoll to remove seminal plasma and spermatozoa resuspended to 350 x 10(6)sperm/mL in a clear Hepes buffered diluent containing either 0, 5, 10, 20, 40 or 80%...
Theriogenology question of the month. Seminoma, spermatocele, sustentacular cell tumor.
Journal of the American Veterinary Medical Association    May 24, 2005   Volume 226, Issue 10 1649-1650 doi: 10.2460/javma.2005.226.1649
Threlfall WR, Robertson JT, Munsterman AS, Oglesbee MJ, Hubbell JA.No abstract available
Comparison of in vitro laboratory analyses with the fertility of cryopreserved stallion spermatozoa.
Theriogenology    April 7, 2005   Volume 64, Issue 6 1422-1439 doi: 10.1016/j.theriogenology.2005.03.006
Kirk ES, Squires EL, Graham JK.Assessing the fertilizing potential of a semen sample is important for effective stallion management and for rapid progress in evaluating new cryopreservation technologies. Unfortunately, sperm motility does not estimate fertility well. These experiments established assays to measure cell viability, acrosomal integrity and mitochondrial function for cryopreserved stallion spermatozoa, using flow cytometry, and determined the variability associated with these assays. Correlations between results for these laboratory assays and stallion fertility were also determined. The inter-assay variability...
Application of MTT reduction assay to evaluate equine sperm viability.
Theriogenology    April 2, 2005   Volume 64, Issue 6 1350-1356 doi: 10.1016/j.theriogenology.2005.02.009
Aziz DM, Ahlswede L, Enbergs H.The assay of MTT reduction depends on the ability of metabolically active cells to reduce the tetrazolium salt (3[4,5-dimethylthiazol-2-y1]-2,5-diphenyltetrazolium bromide) to formazan. This study was conducted to examine and validate of a simple and less costly MTT test in determining equine sperm viability and compare the efficiency of this test with a flow cytometer. Fresh ejaculates from 11 stallions (warm blood) were included in this study. Semen was diluted to 100 million cells/ml in a Hepes 0.1% BSA. The rates of MTT reduction were measured in microtiter plates after incubation for 1 an...
[Horse Advisory Committee: ‘Sperm handling’].
Tijdschrift voor diergeneeskunde    March 31, 2005   Volume 130, Issue 6 179-181 
Stout TA, Seuren-Coppens ML, Parlevliet JM, Colenbrander B.No abstract available
Sperm motility patterns and metabolism in Catalonian donkey semen.
Theriogenology    March 15, 2005   Volume 63, Issue 6 1706-1716 doi: 10.1016/j.theriogenology.2004.07.022
Miró J, Lobo V, Quintero-Moreno A, Medrano A, Peña A, Rigau T.The Sperm-Class Analyzer detected four subpopulations of spermatozoa with different motility characteristics in the ejaculate of the Catalonian donkey. Significant differences (P < 0.001) in the distribution of these subpopulations, as well as in total sperm number and percentage total motility, were seen in the diluted semen of four sampled donkeys. All the ejaculates evaluated showed excellent semen quality characteristics; the sperm they contained was more rapid than horse sperm. Principal components analysis showed sperm l-lactate production to be a good predictor of semen condition. This,...
Relationship of seminal plasma level and extender type to sperm motility and DNA integrity.
Theriogenology    March 15, 2005   Volume 63, Issue 6 1584-1591 doi: 10.1016/j.theriogenology.2004.05.030
Love CC, Brinsko SP, Rigby SL, Thompson JA, Blanchard TL, Varner DD.The relationship between seminal plasma level (0, 10, or 20%) and extender type [Kenney type (EZ-Mixin-CST) or Kenney-modified Tyrodes-KMT] to the susceptibility of sperm DNA to denaturation and sperm motility measures were investigated in cooled (5 degrees C) stallion sperm. Three ejaculates from each of three fertile stallions were collected in an artificial vagina and processed as follows: diluted one part uncentrifuged semen with four parts of extender to a final concentration of 20% seminal plasma in either CST or KMT (20% CST; 20% KMT); diluted to a final concentration of 25 million sper...
High pressure flow cytometric sorting damages sperm.
Theriogenology    March 2, 2005   Volume 64, Issue 5 1035-1048 doi: 10.1016/j.theriogenology.2005.02.002
Suh TK, Schenk JL, Seidel GE.Sexing sperm by high-speed flow cytometry subjects them to high pressure. The routine operating pressure of the MoFlo SX flow cytometer for sperm sorting for commercial production has been 50 pounds/square inch (psi), with a standard 70 microm standard nozzle tip. It was hypothesized that lowering the sorting pressure could reduce sperm damage. Therefore, a series of experiments using semen from six bulls, sorted with three MoFlo SX sorters, was conducted to determine optimal pressure. An additional experiment was done with stallion spermatozoa. In Experiment 1, sorting at 30 psi compared to 5...
Activity of glutathione peroxidase, superoxide dismutase and catalase and lipid peroxidation intensity in stallion semen during storage at 5 degrees C.
Theriogenology    February 24, 2005   Volume 63, Issue 5 1354-1365 doi: 10.1016/j.theriogenology.2004.07.005
Kankofer M, Kolm G, Aurich J, Aurich C.Sperm cell membranes are susceptible to peroxidative damage by an excess of reactive oxygen species (ROS). Antioxidative defence systems consisting of glutathione peroxidase (GSH-Px), superoxide dismutase (SOD) and catalase (CAT) physiologically control the balance between ROS production and neutralization. In the present study the hypothesis was tested that lipid peroxidation occurs during storage of semen at 5 degrees C and that semen extender has positive effects on the antioxidative potential of equine semen. The aim of the study was to determine the activity of GSH-Px, SOD and CAT and the...
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