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Topic:Semen Analysis
Semen analysis involves the evaluation of semen quality to assess reproductive potential and health in horses. This process typically includes the examination of several parameters such as sperm concentration, motility, morphology, and volume. Semen analysis is used in breeding programs to determine the fertility of stallions and to identify any reproductive issues. The collected data can assist in making informed decisions about breeding management and interventions. This page compiles peer-reviewed research studies and scholarly articles that explore the methodologies, findings, and implications of semen analysis in equine reproduction.
Effect of season on some characteristics of stallion semen. Season had a pronounced effect upon seminal pH and refractometer 'protein', total carbohydrate, dry weight, total N2 and lactic acid in seminal plasma of first and second ejaculates. In addition, total seminal volume, spermatozoa per ml and per ejaculate, non-protein sulphhydryl and glycerylphosphorylcholine of second ejaculates were also influenced. There was a season difference in the concentrations of lactic acid in spermatozoa from first and in total N2 from spermatozoa in second ejaculates. The effects of season on seminal plasma were greater than those on spermatozoa. Spermatozoa in firs...
Preservation of differential staining of spermatozoa by formol citrate. Semen from boar, bull, ram, rabbit, reindeer and stallion was diluted in formol citrate or formol saline and stained with eosinnigrosin. The proportion of eosinophilic spermatozoa did not differ from that in fresh semen after storage for 48 hr in the formol diluent at temperatures ranging from 4 degrees C to 40 degrees C. Some samples were kept for periods up to 3 weeks with very little increase in the proportion of eosinophilic spermatozoa.
Influence of ejaculation frequency of stallions on characteristics of semen and output of spermatozoa. Approximately 1 week was required to stabilize the extragonadal sperm reserves in stallions ejaculated daily for 10 weeks. The true daily sperm output of a stallion was equal to the mean daily sperm output of seven ejaculates +/- 1-35 X 10(9) spermatozoa. Mean concentrations of spermatozoa/ml and number of spermatozoa/ejaculate were higher (P less than 0-01) for X1 and X3/week ejaculation frequencies than for a X6/week frequency. Sperm output/week was nearly identical for a X6/week frequency. Sperm output/week was nearly identical for the X3 and X6 frequencies and higher (P less than 0-01) tha...
The relationship between dialy sperm production as determined by quantitative testicular histology and daily sperm output in the stallion. The relationship between daily sperm productions (DSP) and daily sperm output (DSO) was determined in eleven stallions. The DSO was determined by collecting single ejaculates, with an artificial vagina, at 24-hr intervals. The stallions were killed 24 hr after the last collection and the DSP was determined by quantitative testicular histology. The mean DSP was 8-0 X 10(9) (S.E. +/- 0-4 X 10(9), and the mean DSO was 7-0 X 10(9) (S.E. +/- 0-4 X 10(9)). It was estimated that 87% of the spermatozoa produced by the testes were harvested. The correlation between DSP and DSO was 0-80 (P less than 0-0...
Biochemistry of stallion semen. Stallion semen has several chemical characteristics not commonly encountered in other animals. It contains very little fructose and the spermatozoa possess only limited fructolytic ability under anaerobic conditions. By determining some of the characteristic constituents such as ergothioneine, citric acid, glycerylphosphorylcholine and certain glycosidases, it is possible to obtain a quantitative measure of the secretory contribution of the ampulla, seminal vesicle and epididymis, respectively, towards the final composition of the whole ejaculate. By analysing separately the various fractions ...
Characteristics of the successive jets of ejaculated semen of stallions. The use of an 'open' artificial vagina made it possible to separate the individual jets in the ejaculate of the stallion. A total of 132 jets were collected in this way from twenty-one ejaculates. After macro- and microscopic examination and sperm counting, glycerylphosphorylcholine (GPC), ergothioneine and fructose levels were determined for every jet. The values obtained for the first three jets were similar and accounted for about 76% of all spermatozoa, and 70% of GPC. These jets also contained the highest concentration of ergothioneine and fructose.
Immature germ cells in the semen of thoroughbred stallions. Small but significant numbers of primary and secondary spermatocytes and spermatids have been observed in the semen of some Thoroughbred stallions. Extensive histological examination of the testes of affected animals has not been undertaken but in one young stallion which died as the result of a leg injury, the premature dehiscence of these cells seemed to be related to segmental defects within the seminiferous tubules. The causes of lesions leading to premature shedding of germ cells are discussed.
A study of the morphology of stallion semen during the breeding and non-breeding seasons. Season was shown to markedly influence semen characteristics of stallions in Holland, including ejaculate volume, sperm motility, total number of spermatozoa/ejaculate and the percentage of spermatozoa showing morphological abnormalities. Maintenance of normal stallions in continuous light during the winter months and administration of a vitamin and mineral supplement to sub-fertile stallions before the start of the breeding season appeared to improve spermatogenesis significantly.
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.
Spermatogenesis and duration of transit of spermatozoa through the excurrent ducts of stallions. The cycle of the seminiferous epithelium was divided into eight stages on the basis of meiotic divisions, shape of the spermatid nuclei and location of the spermatids with elongated nuclei. Duration of this cycle was 12-2 days (S.E. +/- 0-1) as determined by [3H]thymidine injections and autoradiography. The life-span of primary spermatocytes was 19-0 days, secondary spermatocytes 0-7 days, spermatids with round nuclei 8-7 days, and spermatids with elongated nuclei 10-1 days. Labelled spermatozoa entered the caput epididymidis 35 days, and appeared in the ejaculate 39-9 days, after the isotope ...
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%.
Semen characteristics in thyroidectomized stallions. Three Quarter-horse stallions were surgically thyroidectomized at 18 months of age. Weekly semen collections were made from these and three control stallions from 25 to 39 months of age. Although the induced state of hypothyroidism in young stallions has a depressing effect on libido and general animation and can be corrected by thyroprotein supplementation, semen characteristics, testicular histology and fertility are not affected by the operation.
Influence of mare uterine tubal fluids on the metabolism of stallion sperm. Three experiments were conducted on the metabolism of stallion sperm. In experiment 1, whole and washed sperm were incubated under aerobic and anaerobic enviroments and analyzed before and after controlled incubation for motility, pH, lactic acid, glucose, fructose, and O2 comsumption. In experiment 2, whole and washed sperm were incubated aerobically and anaerobically with and without uterine tubal fluids. Experiment 3 was the same as experiment 2, except added substrates of glucose and lactic acid were studied. The same examinations were made in experiments 2 and 3 as for experiment 1. Motil...
[Relationship of citric acid concentration to various quality indices of the equine ejaculate]. The paper describes the relation of citric acid to other chemical and biological indices of the fertility of stallion sperm. A positive relation was found between citric acid and the density and motility of spermatozoa, to the concentration of ergothioneine, and hemolytic activity, and a negative relation to pH and to the polarographic activity of proteins. Attention is drawn to the important nutritional function of citric acid.
[An immunologic study of hyaluronidase of different animal origin]. Studied was the antigenic relatedness of hyaluronidase contained in the semen of breeder animals of homologic and heterologic species. The experiments were carried out by means of the immunodiffusion and the immunoelectrophoretic methods. The results obtained showed that the seminal hyaluronidase of bulls, rams and bucks is antigenically related, and that of stallions, boars and rabbits does not exhibit antigenic relatedness. Stallion semen is closely related antigenically with the above-mentioned three animal species' semen as manifested by two precipitation bands, but these are not identical...
Analysis of the pattern of ejaculation in stallions. The emission of stallion semen was studied with the aid of
an `open' Krak\l=o'\w-72Model artificial vagina. The pattern of mating
behaviour was constant in all copulations observed : a mean number of
seven intravaginal thrusts was required to elicit ejaculation. The
pressure within the vestibule of the artificial vagina averaged 66 mmHg
at the beginning of copulation, 142 mmHg just before ejaculation, and
70 mmHg during the emission of semen. Emission appeared to be a more
variable process. Five to ten jets were observed; the mean number was
eight. The early jets occurred under high pr...
