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At least 19 recordsLinked to original sources
PubMed1995

Relationship among seminal characteristics, fertility and suitability for semen preservation in draft stallions.

Seminal characteristics, fertility and the response to semen preservation (liquid storage and cryopreservation) were evaluated in 4 Draft stallions (Percheron 2, Breton 2). Seminal characteristics (gel-free volume, sperm concentration, sperm morphology, percentage of motile spermatozoa) were assessed in 5 ejaculates from each of the 4 stallions. The fertility of the stallions was calculated retrospectively as the accumulated pregnancy rate over 3 breeding seasons. Five ejaculates from each of the stallions were subjected to liquid storage at 5 degrees C. The percentage of motile spermatozoa (PMS) was assessed at 0, 24, 48 and 72 hr. Cryopreservation was done with a glucose-EDTA-lactose egg yolk extender and a skim milk-based extender containing clarified egg yolk (4 replicates per stallion). PMS and the percentage of spermatozoa with an intact plasma membrane (IPM) were evaluated before and after freezing. Although semen characteristics and fertility were within a physiological range, significant differences among stallions were found for gel-free volume, percentage of morphologically normal spermatozoa, PMS, and fertility but there was no clear relationship between these parameters. The response to liquid storage of diluted semen samples differed among stallions and best results were obtained in a stallion with the highest initial motility. The freezability of semen from the 4 stallions was poor with both of the freezing protocols (PMS range 13.8%-26.3%; IPM range 19.5%-38.0%). Results of liquid storage and cryopreservation were not correlated in individual stallions and were not related to their fertility. Since predictability for the response to semen preservation is low, the suitability of individual stallions for semen preservation has to be examined carefully.(ABSTRACT TRUNCATED AT 250 WORDS)

Animals↗
PubMed1978

Semen preservation in Macaca fascicularis.

Semen was collected from adult male Macaca fascicularis using a rectal probe for electro-ejaculation. The effect on sperm motility of varying semen extender egg yolk concentration, pH, glycerol concentration, and equilibration times of sperm with glycerol was examined. No significant difference was observed between motilities at extender egg yolk concentrations of 10% to 40%. Progressive motility was significantly greater at pH 7.2 and 8.0 than at 5.8, 6.5, and 8.7 (p less than 0.05). Glycerol concentrations of 7% and 10% yielded optimum progressive motility after freezing. A 1-minute equilibration of semen in extender containing glycerol resulted in greater sperm motility after freezing than did equilibration for 25 or 45 minutes.

Animals↗
PubMedDate not supplied

[The value of donor sperm in intra-cytoplasmic sperm injections? The French Centers for Semen Preservation policy].

Some IVF laboratories ask for donor's semen during an ICS attempt if retrieval of husband's sperm is unsuccessful. The French Centers for Semen preservation (CECOS) consider that this request is not acceptable for legal, psychological and ethical considerations. Legal consent may not be ambiguous. The psychological lost of biological fatherhood should be totally assumed before undertaking conception with donor's semen. ICSI should be started only if it is most likely to succeed. For all these reasons, CECOS refuse to modify the strategy of procreatione during the course of an attempt.

Ethics, Medical↗
PubMed1983

Semen quality in relation to semen preservation.

A goal of research in laboratory evaluation of semen has been ultimately to predict the fertility achievable with use of that semen. This would permit evaluation of the male and ejaculate. For artificial insemination, semen viability becomes a measure of man's interaction with that semen in an effort to preserve its functional life. Man's efficiency in developing successful methods of semen preservation are, therefore, contingent upon the relationship of tests of semen quality and fertility. Problems discussed are those associated with identification of the most appropriate tests of spermatozoan viability important to fertility. These problems reside predominantly in poor repeatability of many tests (objectivity versus subjectivity), the interaction of semen quality and quantity in the inseminate, the effect of latent cell injury encountered in some systems of preservation (example frozen semen), and identification of viability traits of spermatozoa important to their retention and transport in the female reproductive tract as well as their ability to fertilize the egg and sustain embryogenesis. A case is established for the use of more than one viability test or semen trait for evaluating systems of semen preservation.

Animals↗
PubMed1978

Current status of semen preservation in the ram, boar and stallion.

From the studies cited it was concluded that short and long term preservation of stallion semen has encountered major obstacles. Fertilizing capacity of extended or extended and cooled spermatozoa has been impaired. With the hydrogen ion extenders, the fertility was depressed either with or without glycerol when the semen was inseminated immediately after extension. With the cream-gel extender, fertility was not impaired when inseminated immediately after extension, but was impaired after storage at 5 C for 24 hr or in the presence of glycerol. The fertilizing capacity of extended frozen spermatozoa particularly from some stallions has been more adversely affected than that of others. These studies show that the pregnancy rate range was from 50 to 80% for raw semen from the same stallion used in the frozen studies. Pregnancy rate with this magnitude of difference must be carefully weighed in applying the results from a few stallions to the population. Sufficient information has been generated to suggest that the preservation of stallion spermatozoa is possible but the fertilizing capacity is impaired. Causes of this impairment must be further investigated. When this is accomplished, the number of motile spermatozoa needed per insemination and the frequency of insemination required for optimal fertilization reported in this review must then be reevaluated.

Animals↗
PubMed1990

Fertility test for ram semen preserved at ambient temperatures by discontinuous flow dialysis.

The effect of two insemination doses (250 vs 500 x 10(6) spermatozoa) and three storage periods (0,1 or 2d) on the fertility of ram semen preserved at ambient temperatures by discontinuous flow dialysis were investigated in sheep (n=54). The 21-d nonreturn rates were 55.6, 44.4 and 27.8% for the three storage periods, and 44.4 and 40% for the two insemination doses, respectively. The corresponding lambing rates were 38.9, 16.7 and 11.1% for the three storage periods, and 25.9 and 18.5% for the two insemination doses, respectively. There were no significant differences between any of the treatments (P>0.05).

Journal Article↗
PubMed1996

Oestrous synchronization, semen preservation and artificial insemination in the Mohor gazelle (Gazella dama mhorr) for the establishment of a genome resource bank programme.

Gazella dama mhorr is an endangered species with an extant population of about 190 animals distributed between several zoos. Semen was collected by electro-ejaculation from 12 adult males, and cryopreserved in TEST-yolk diluent containing 6% glycerol. The effects of the concentration of egg yolk (5%, 10% and 20%) and the presence or absence of sodium triethanolamine lauryl sulfate (equex) on sperm motion and acrosomal integrity after thawing were examined. Increasing concentrations of egg yolk resulted in more acrosomal damage and poorer motility after thawing. The presence or absence of equex had no effect on either parameter. The frozen spermatozoa were used in an insemination trial, in which 13 females were treated with intravaginal progesterone-releasing devices to synchronize oestrus. Seven females were inseminated with frozen-thawed semen 48 h after removal of the devices, and six were inseminated after 60 h. Three females in the first group and one in the second group became pregnant. However, only one pregnancy (from the 48-h group) was carried to term. The study demonstrated the feasibility of applying artificial insemination in this species, but revealed that a number of outstanding technical problems remain to be solved.

Acrosome↗
PubMedDate not supplied

Effect of cryoprotective media and freezing techniques on human semen preservation.

With the growing programme of IVF--Et at Lagos University Teaching Hospital the need arise to establish a sperm bank to meet the ever increasing demand at the Hospital for artificial inseminations and in-vitro fertilisation. Fifteen semen samples with count range 50--200 million/ml and motility 30--82% were used. The effectiveness of five synthetic cryoprotectants I, II, III, IV and V and three freezing techniques A, B, and C in cryoperserving human semen were studied. The results were assessed by comparing prefreeze and post thaw sperm motility. Our results using ANOVA (analysis of variance) demonstrated that (1) 7.5% glycerol produced better results than all the other cryoprotectants. (2) Initial freezing in ultralow electrical freezer (-90 degrees c) before storage in liquid nitrogen (-196 degrees c) produced a significantly better post-thaw motility and this was maintained for 4 weeks (table 2). It was therefore concluded that sperm banking can be accomplished in a relatively simple and reliable way using 7.5% glycerol alone and initial freezing in ultralow electrical freezer before storage in liquid nitrogen.

Analysis of Variance↗
PubMed1996

[Semen preservation and gonadal toxicity in the treatment of non Hodgkin lymphoma. Experience at the Gustave-Roussy Institute from 1980 to 1993].

More than 50% of patients with non Hodgkin's lymphomas (NHL) are long-term survivors. We have retrospectively analysed the indication of semen cryopreservation and late gonadal toxicity for 213 males patients consecutively treated at the Gustave Roussy institute from 1980 to 1993 for NHL. The mean age was 30 years (15-42) and all patients received chemotherapy with or without radiotherapy. Initial spermograms and cryopreservation of semen were obtained in only 24 patients (half of them between 1991 and 1993). Spermogram characteristics were as follows: 11 normal; 13 abnormal with oligospermia (n = 7), asthenospermia (n = 7), and teratospermia (n = 8). No relation was found between the pretherapeutic status and the semen sample quality. Cryopreservation was possible in only 22 cases, and among the 16 surviving patients, two have undergone insemination and the remaining 14 are maintaining their cryopreserved semen samples. Long-term gonadal toxicity was assessed on spermograms of nine patients: three of whom had evidence of return to pretherapeutic status. FSH levels were assayed for 48 patients: at a threshold of 8 g/m2 of cyclophosphamide, 86% of patients had elevated values (P < 10(-6). Cumulated doxorubicin doses were not correlated with FSH elevation. Five patients have had children after treatment. In conclusion, chemotherapy for NHL seems to induce an intermediate level of gonadal toxicity which is between that of MOPP and ABVD. Complete information about gonadal toxicity of chemotherapy is warranted for young male patients who are to receive chemotherapy and semen cryopreservation should be suggested to this population.

Adolescent↗
PubMed1989

Effects of semen preservation on boar spermatozoa head membranes.

Head plasma membranes were isolated from the sperm-rich fraction of boar semen and from sperm-rich semen that had been subjected to three commercial preservation processes: Extended for fresh insemination (extended), prepared for freezing but not frozen (cooled), and stored frozen for 3-5 weeks (frozen-thawed). Fluorescence polarization was used to determine fluidity of the membranes of all samples for 160 min at 25 degrees C and also for membranes from the sperm-rich and extended semen during cooling and reheating (25 to 5 to 40 degrees C, 0.4 degrees C/min). Head plasma membranes from extended semen were initially more fluid than from other sources (P less than 0.05). Fluidity of head membranes from all sources decreased at 25 degrees C, but the rate of decrease was significantly lower for membranes from cooled and lower again for membranes from frozen-thawed semen. Cooling to 5 degrees C reduced the rate of fluidity change for plasma membranes from the sperm-rich fraction, while heating over 30 degrees C caused a significantly greater decrease. The presence of Ca++ (10 mM) lowered the fluidity of the head plasma membranes from sperm-rich and extended semen over time at 25 degrees C but did not affect the membranes from the cooled or frozen-thawed semen. The change in head plasma membrane fluidity at 25 degrees C may reflect the dynamic nature of spermatozoa membranes prior to fertilization. Extenders, preservation processes and temperature changes have a strong influence on head plasma membrane fluidity and therefore the molecular organization of this membrane.

Animals↗