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At least 73 records · Page 4Linked to original sources
PubMed2000

Influence of initial semen quality on the integrity of human sperm DNA following semen processing.

OBJECTIVE: To examine and compare the effects of density-gradient centrifugation on the integrity of sperm DNA from the semen of both fertile and infertile men. DESIGN: Prospective, observational study. SETTING: University infertility clinic. PATIENTS: Forty-four nonazoospermic, infertile men and nine fertile controls. INTERVENTIONS: Semen samples were processed by density-gradient centrifugation. Sperm motility and sperm chromatin structure (evaluated by flow cytometry analysis of acridine orange-treated spermatozoa) were monitored before and after semen was processed. MAIN OUTCOME MEASURES: Sperm motility and DNA integrity. RESULTS: Following density-gradient centrifugation, mean sperm motility (+/-SEM) improved significantly compared to whole semen in samples from fertile and infertile men, respectively (71 +/- 6 vs. 49 +/- 7% and 56 +/- 3 vs. 44 +/- 3%, P<0.05). However, the percentage of sperm with denatured DNA increased compared to whole semen after processing of samples from infertile (25 +/- 3 vs. 15 +/- 2%, P<0. 01) but not fertile men (9 +/- 3 vs. 8 +/- 2%, P>0.05). CONCLUSIONS: Our data indicate that the potential detrimental effect of density-gradient centrifugation on sperm DNA integrity is related to the initial semen quality. These data urge us to examine our current sperm-processing techniques to minimize sperm DNA damage.

Acridine Orange↗
PubMed2003

Concentrations of endogenous prostaglandin F2alpha in boar semen and effect of a 72-h incubation period on exogenous prostaglandin F2alpha concentration in extended boar semen.

PGF2alpha in semen has been shown to induce uterine contractions, thereby, facilitating sperm transport during fertilization. Previously, we demonstrated that extended boar semen used in artificial insemination does not increase myometrial contractility, but PGF2alpha supplementation did. In this study, we determined the concentrations of endogenous PGF2alpha in pre-sperm and sperm-rich fractions of the boar ejaculate and examined whether changes in the concentration of exogenous PGF2alpha occurred when added to extended boar semen after 72-h incubation at a 17 degrees C storage temperature. Concentrations of endogenous PGF2alpha (n = 10 boars) in pre-sperm and sperm-rich fractions were 69.6 +/- 7.6 and 58.9 +/- 4.4 pg/ml, respectively. No differences were observed in the concentrations of exogenous PGF2alpha in the extended boar semen at 0 h (59.3 +/- 3.3 microg/ml) and after a 72-h incubation period (52.0 +/- 2.1 microg/ml). These results suggest that the concentration of endogenous PGF2alpha in boar semen used for artificial insemination is < 100 pg/ml. The concentration of exogenous PGF2alpha in the extended boar semen did not differ after 72 h, which indicates that it is not metabolized during this period of time.

Animals↗
PubMed1978

A new poultry semen extender 3. Effect of storage conditions on the fertilizing capacity of chicken semen stored at 5 degrees C.

Semen from adult Leghorns was subjected to one of five treatments during storage at 5 degrees C. for periods of up to 24 hr. The effects of dilution rate, storage temperature, presence of seminal plasma, presence of visible light and the semen to air ratio in the storage vessel were studied on the fertilizing capacity of spermatozoa after 0, 4 and 24 hr. of storage. The results indicated that the fertilizing capacity of chicken semen stored at 5 degrees C. was equal to that of the unstored controls when semen was diluted and exposed to a light intensity of 129 lux during the entire storage period. Viability of semen stored at 5 degrees C. for 24 hr. was unaffected by storage temperature (5 vs 15 degrees C.), the presence or absence of seminal plasma, or the semen to air ratio in the storage vessel.

Air↗
PubMed1992

Effect of modifications of semen diluent with cell culture serum replacements on fresh and stored turkey semen quality and hen fertility.

Two commercially available serum replacements formulated as supplements to somatic cell culture media were used with a turkey semen diluent to determine their effect on semen quality and spermatozoal fecundity before and after semen storage for 24 h. Progressive motility estimates (visual) and spermatozoal motility characteristics estimated by a computer-assisted semen analysis system, and sperm viability tests (the ethidium bromide exclusion procedure and a sperm stress test) were used to evaluate the semen. Although the presence of the serum replacements significantly increased spermatozoal motility, fertility was not augmented by the presence of the serum replacements. Computer-derived spermatozoal velocity and the percentage of nonviable spermatozoa estimated by the sperm stress test were negatively correlated with hen fertility. It was concluded that although the serum replacements augmented some spermatozoal motility characteristics, they failed to improve the fecundity of spermatozoa either before or after semen storage for 24 h.

Analysis of Variance↗
PubMed2004

Intrauterine insemination (IUI) pregnancy outcome is enhanced by shorter intervals from semen collection to sperm wash, from sperm wash to IUI time, and from semen collection to IUI time.

OBJECTIVE: To determine whether IUI pregnancy was affected by [1] place of semen collection (home vs. clinic), and [2] intervals from collection to sperm wash (C-SW), from sperm wash to IUI (SW-IUI), and from collection to IUI (C-IUI). DESIGN: Retrospective study. SETTING: Infertility clinic. PATIENT(S): Sixty-two couples in 132 cycles. INTERVENTION(S): Clomiphene citrate (CC) or hMG, plus hCG, and IUI. MAIN OUTCOME MEASURE(S): Ultrasonographic detection of fetal heart beat(s). RESULT(S): Semen collection at clinic resulted in a higher pregnancy rate than collection at home in hMG-treated (44% vs. 18%; P=.03) but not in CC-treated women (9% vs. 9%; P=.93). Intervals of C-SW, SW-IUI, and C-IUI were shorter in pregnant than in nonpregnant hMG-treated women (27 vs. 41 minutes, 42 vs. 85 minutes, and 99 vs. 156 minutes, respectively; P< or =.01) but not in CC-treated women (28 vs. 38 minutes, 51 vs. 63 minutes, and 109 vs. 131 minutes, respectively; P> or =.19). Semen processed within 30 minutes after collection resulted in a higher pregnancy rate than that processed 31-60 minutes after collection in hMG-treated (48% vs. 18%; P=.02) but not in CC-treated women (10% vs. 8%; P=.81). Intrauterine insemination performed within 90 minutes of collection resulted in a higher pregnancy rate than IUI performed at 91-120 minutes or >120 minutes after collection in hMG-treated (99% vs. 22% and 7%, respectively; P<.0001) but not in CC-treated women (11%, 4%, and 10%, respectively; P> or =.46). CONCLUSION(S): For i.u.i. with hMG but not CC, semen collection at the clinic is more effective than, and should be chosen over, collection at home. Delaying semen processing from 30 minutes up to 1 hour and/or delaying IUI from 90 minutes up to 2 hours after collection compromises the pregnancy outcome in hMG-IUI cycles. Semen specimens should be processed as soon as just after liquefaction and within 30 minutes of collection, and IUI performed as soon as just after processing and within 90 minutes of collection.

Adult↗
PubMed2006

Within- and between-subject variation in semen parameters in infertile men and normal semen donors.

OBJECTIVE: To determine within- and between-subject variation of semen parameters in infertile and normal men. DESIGN: Retrospective analysis of 74 infertile men and 65 normal men producing five or more ejaculates each. SETTING: Clinical andrology laboratory. SUBJECT(S): Men presenting to an infertility clinic for semen analysis and normal men providing donor semen for cryopreservation. INTERVENTION(S): None. MAIN OUTCOME MEASURE(S): Within-subject coefficients of variation (CVw) and between-subject coefficients of variation (CVb), calculated for sperm count, motility, and velocity, semen volume, and motility and velocity after cryopreservation. RESULT(S): The number of ejaculates ranged 5-20 in patients (479 total) and 5-136 in donors (2,043 total). Sperm counts, motility, and velocity were statistically greater in donors, whereas semen volume was significantly greater in patients. The CVw in patients and donors was greatest in sperm counts (54.2% and 45.8%, respectively) and lowest in velocity (20.1% and 19.9%, respectively). The CVb in patients and donors was markedly higher than CVw for all parameters in both patients and donors. The CVw was lower, and the CVb was higher, in donors compared with patients. The CVw was not affected by age of the individual or abstinence period. Cryopreservation resulted in a marked increase in variability. Intraclass correlations indicated that a minimum of three semen samples were required to achieve reliability. CONCLUSION(S): These data indicate large within- and between-subject variation in sperm parameters, especially sperm count, in both patients and healthy donors, and further substantiate the need for measurement of multiple ejaculates before characterizing a man as normal or infertile.

Adult↗
PubMed1999

Semen specific gamma-glutamyltransferase carries ABH antigens: a sandwich ELISA for simultaneous semen detection and its ABO blood typing.

Semen type of gamma-glutamyltransferase (gamma-GTP) is different from the membrane bound type of the enzyme in both biochemical and immunological properties, and consists of two subunits (150 and 95 kDa). We found that anti-ABH antibodies recognize a 150-kDa subunit of seminal gamma-GTP by Western blot and immunoprecipitation analyses. Using SG2, one of anti-semen specific gamma-GTP monoclonal antibodies which we had produced, and anti-ABH antibodies, we established a sandwich ELISA for identifying human seminal gamma-GTP and its ABO type simultaneously. This sandwich ELISA allows ABO typing of highly diluted semen. The dilutions for ABO typing were 10(5) times for A or O, and 10(4) times for B. Furthermore, ABO typing of semen was successfully performed by this ELISA, even in the mixed presence of vaginal fluid, saliva and blood. Thus, seminal gamma-GTP carries ABH antigens and the sandwich ELISA with SG2 and anti-ABH antibodies enables ABO typing of semen. The sandwich ELISA is extremely useful for ABO typing originated from semen in the mixture of biological fluids.

ABO Blood-Group System↗
PubMed1980

Artificial insemination with donor semen mixed with semen of the infertile husband.

Mixing an oligoasthenospermic husband's semen with that of a donor prior to insemination (AIM) has been criticized, since such semen may contain antibodies which could interfere with normal sperm function. The efficacy of AIM was reviewed in 227 patients who underwent AI with frozen donor semen. Thirty-four patients requested AIM and thirteen conceived (38.2%). Seven who failed to conceive after AIM changed to donor insemination (AID), and two conceived. One hundred and ninety-three patients had AID alone, and eighty conceived. Thus, 200 patients had AID, with 82 pregnancies (41%). There were no significant differences between the AIM and AID groups with regard to age, prior fertility, and additional infertility factors. The conception rates between groups were not significantly different. Pregnancy rates per cycle of AI and dropout rates were also similar. Postinsemination testing after AIM did not reveal any effect of husband's semen upon donor spermatozoa. This study failed to show a deleterious effect of semen from azoospermic or oligoasthenospermic, infertile men upon normal semen, as used in AIM.

Female↗
PubMed2000

Hepatocyte growth factor in human semen and its association with semen parameters.

Hepatocyte growth factor (HGF) is a structurally unique growth factor with potent motogenic (motility inducing) effects. Studies in the murine male genital tract have suggested important associations between HGF and the acquisition of sperm motility during epididymal maturation. The aim of this study was, therefore, to determine the concentration of HGF in human semen and assess its correlation, if any, with sperm motility and other semen parameters. Semen samples were collected by masturbation and analysed using standard procedures. HGF concentrations were measured in duplicate using an enzyme-linked immunoassay technique. Total protein estimations were also made in a subset of samples. The 95 subjects were divided into three groups for analysis: normozoospermic, subnormal semen and azoospermic. HGF was detected in all samples (median 0.456, 25th centile 0.388, 75th centile 0.556 ng/ml). No significant correlations were found between semen HGF concentrations and sperm concentration, motility, total sperm count or total motile count. There were no significant differences in mean HGF concentrations between the three subgroups. In conclusion HGF is present in human semen in significant quantities. The data do not suggest HGF concentrations are correlated with parameters of sperm motility.

Adult↗
PubMed2006

Detection of human immunodeficiency virus-1 RNA and DNA by extractive and in situ PCR in unprocessed semen and seminal fractions isolated by semen-washing procedure.

BACKGROUND: To determine the presence of human immunodeficiency virus-1 (HIV-1) viral RNA/DNA in whole semen, in properly isolated seminal fractions and in spermatozoa after swim-up, by extractive nested PCR and to compare the detection of HIV DNA by in situ PCR (IS-PCR) with the results of nested PCR. METHODS: We tested HIV-1 RNA and DNA by nested PCR in semen and in seminal fractions from 55 patients. Non-spermatic cells and spermatozoa pellet fractions from 10 HIV-1-positive and five HIV-1-negative men were tested for proviral DNA by IS-PCR. RESULTS: All samples of spermatozoa recovered after sperm washing were free of HIV RNA. HIV RNA tested positive in seven (13%) seminal plasma samples and only in two (4.2%) whole semen of these same samples. Of the seven seminal plasma samples testing positive for HIV RNA, four men had elevated blood viral load and three an undetectable viraemia. HIV DNA by IS-PCR turned positive in three of five samples in semen of HIV-noninfected men. CONCLUSION: HIV RNA/DNA detection in the semen of HIV-infected men proves the efficacy of sperm washing with swim-up of spermatozoa. It is recommended that nested PCR be conducted on purified seminal compartments. IS-PCR is inadequate for detecting HIV in semen.

Adult↗
PubMed1999

Effects of frequency of semen collection on quantitative and qualitative characteristics of semen in turkey breeder males.

The effects of various frequencies of semen collection on several quantitative and qualitative semen characteristics were investigated in adult turkey breeder males (30 to 40 wk of age). In Experiment 1, a total of 35 males were first trained for semen collection (twice a week for 2 consecutive wk), and then divided into five groups (seven males each), each group being collected either once every 2 wk, once every week, twice every week, three times every week (each for 4 wk) or five to seven times per week (each for 2 wk). Volume, sperm concentration, and sperm number per ejaculate were determined for each ejaculate. No significant differences between groups were observed for sperm concentration (P > 0.05), but males collected once every 2 wk, once per week, or twice per week had larger volumes than males collected at higher frequencies (P < 0.05). Thus there were significant differences for sperm number per ejaculate between groups (P < 0.05). Also, daily semen output (DSO) was markedly increased in males collected at the highest frequencies (e.g., DSO = 0.62 x 10(9) and 1.93 x 10(9) in males collected once and five times per week). Finally, in euthanatized birds (36 wk) no differences between groups were observed for body weight (25.8 +/- 1.7 kg), testicular weight (51.5 +/- 2.2 g), or total number of elongated spermatids per male (14.0 +/- 0.8 x 10(9)). In Experiment 2, 35 males were distributed into groups and collected under the same conditions as in Experiment 1. Besides quantitative analyses of ejaculates (volume, sperm concentration, and sperm per ejaculate), sperm viability between groups was also tested using the Sybr14/PI fluorescence test. Our results demonstrated: 1) a favorable effect of high semen collection frequencies on sperm viability and, 2) a marked decline in sperm viability during the first 2 d following a 2-d resting period in males collected five times a week. We concluded that turkey males express their optimal reproductive capacity more efficiently when semen collection is undertaken at a high rather than a low frequency.

Analysis of Variance↗
PubMed1997

Detection of human herpesvirus 8 DNA in semen from HIV-infected individuals but not healthy semen donors.

OBJECTIVE: To ascertain the prevalence of Kaposi's sarcoma-associated herpesvirus (KSHV), also known as human herpesvirus (HHV) type 8, and cytomegalovirus (CMV) DNA in semen was investigated. METHODS: Amplification by nested polymerase chain reaction was used to detect viral DNA sequences in samples from 24 HIV-infected gay men, 15 of them with Kaposi's sarcoma (KS), and 115 healthy donors. RESULTS: Six of the 24 HIV-infected patients had detectable HHV-8 DNA in their semen: three of the 15 patients with KS and three of the nine patients without KS. CMV DNA was detected in 20 semen samples from HIV-infected patients. None of the semen samples from healthy donors had detectable HHV-8 DNA and rates of CMV DNA detection were low (3%). CONCLUSIONS: The study demonstrates the presence of HHV-8 in semen from HIV-infected individuals with, or at risk, of developing KS and the potential for sexual transmission of the virus. We found no evidence of HHV-8 in the semen of HIV-uninfected donors.

Cytomegalovirus↗
PubMed1998

Changes in semen quality and in vitro sperm capacitation during various frequencies of semen collection in dogs with both asthenozoospermia and teratozoospermia.

Eight male dogs with both asthenozoospermia and teratozoospermia were used in this study. In experiment 1, semen was collected 10 times at intervals of 48 hr, 24 hr and 12 hr in 4 of the 8 dogs, and the semen quality was evaluated. In experiment 2, semen was collected 5 times at 24-hr intervals in the other 4 dogs. The spermatozoa collected on day 1 and day 5 were incubated for 4-6 hr in Canine Capacitation Medium, and the percentages of hyperactivated sperm (%HA), acrosome-reacted sperm (%AR), and the zona pellucida-binding sperm count (ZP sperm count) were assessed. The results of experiment 1 showed that the percentage of motile sperm increased and the percentage of abnormal sperm decreased markedly as the intervals between semen collections became shorter. When semen was collected at 12-hr intervals, the percentage of motile sperm increased from about 65%, the value before frequent collection was started, to about 80%, and the percentage of sperm with abnormal tails decreased from 30% to 15%. In experiment 2, the percentages of HA and AR, and the ZP sperm count in specimens collected on day 5 were higher than those in specimens collected on day 1, and the differences in % HA and in ZP sperm count were significant (P<0.05). The results demonstrated that sperm motility, abnormality, and potential fertility in dogs with asthenozoospermia and teratozoospermia can be temporarily improved by frequent semen collection.

Acrosome↗
PubMed1985

Semen characteristics in pubertal boys. I. Semen quality after first ejaculation.

Semen specimens from 134 pubertal boys were examined, and some 274 assays were made. An analysis of the biological quality of semen in relation to the period of time after first ejaculation brings high values of statistical dependence of the volume of semen, its liquefaction, spermatozoal concentration, percentage of morphologically normal forms of spermatozoa, and normal spermatozoal motility on the period of time after first ejaculation. Normal figures for semen volume, semen liquefaction, spermatozoal concentration, and morphology are observed 12-14 months after first ejaculation. The percentage of normally motile spermatozoa becomes standard 21-23 months after first ejaculation. There were changes in semen characteristics from azoospermia through cryptozoospermia, oligozoospermia, and asthenozoospermia to normospermia. Azoospermia dominates until the fifth month after the first ejaculation, oligozoospermia from the sixth to the eleventh month, asthenozoospermia from the twelfth to the twentieth month, and normospermia from the twenty-first month.

Adolescent↗
PubMed1978

A new poultry semen extender 2. Effect of the diluent components on the fertilizing capacity of chicken semen stored at 5 degrees C.

The major objective of this study was to assess the relationship of various components of the Beltsville Poultry Semen Extender (BPSE) to the maintenance of the fertilizing capacity of chicken semen stored at 5 degrees C. A secondary objective was to rest the effectiveness of certain chemical additives on maintining the fertilizing capacity of stored semen. The data indicate that the components of the BPSE which contribute most to the preservation of semen were sodium glutamate and potassium phosphate. Also the high level of potassium in the BPSE was critical to the survival of spermatozoa during low temperature storage. Although the fructose component of the BPSE was not a significant factor during storage, attempts to substitute fructose with other carbohydrates resulted in a reduction in fertility. The addition of gentamicin sulfate (100 to 200 microgram/ml.), or pasteurized milk (10% v./v.) to the BPSE did not significantly alter the fertilizing capacity of semen stored for 24 hr., whereas similar levels of whole egg, egg yolk, egg albumen or seminal plasma had a depressive effect. The data in this study clearly indicate that components of and additions to the BPSE were responsible for the maintenance of only about 50 to 60% of the fertilizing capacity of chicken semen stored for 24 hr. at 5 degrees C.

Animals↗
PubMed1992

Transferrin (TF) typing from semen stains using isoelectric focusing and immunoblotting: correlation of TF types among blood, semen, urine, and vaginal secretion.

We describe a method for obtaining nondistorted and reproducible transferrin (TF) typing from liquid semen and semen stains. Isoelectric focusing of TF isoproteins on polyacrylamide gel (IEF-PAGE, pH 4 to 6.5) was accomplished using a 0.5 mm thick gel. The separated isoproteins were then visualized by immunoblotting with TF-specific antibody. Pretreatment of semen samples with neuraminidase enhanced the TF band resolution. The method was reliable, sensitive and simple, with a high resolution. When maintained at room temperature, laboratory-prepared semen stains were TF-typable for up to at least 50 weeks. The TF types in semen stains were correlated with the types found in the corresponding blood and urine samples. TF typing could therefore provide an additional discriminant characteristic in the forensic examination of semen stains. An evaluation of TF typing by IEF-PAGE and immunoblotting was also performed on casework samples submitted to our laboratory.

Adult↗
PubMed1996

Data from men in greater Seattle area reveals no downward trend in semen quality: further evidence that deterioration of semen quality is not geographically uniform.

OBJECTIVE: To determine whether there has been a decline in semen quality in a group of healthy men during the past 21 years. DESIGN: Retrospective analysis of the relationship between time and changes in semen parameters over 21 years using regression analysis. SETTING: A tertiary university center. PATIENTS: Five hundred ten healthy, normal men who donated multiple semen samples as participants in clinical studies between 1972 and 1993. MAIN OUTCOME MEASURES: Sperm concentration, semen volume, total numbers of sperm per ejaculate, and percent spermatozoa with normal morphology. RESULTS: There was no decrease in sperm concentration, semen volume, total number of sperm per ejaculate, and percent normal sperm morphology in 510 healthy men studied between 1972 and 1993. CONCLUSION: We conclude that in this population of healthy young men there has not been any decline in semen quality in the past 21 years.

Fertility↗
PubMed1997

Semen production by the emu (Dromaius novaehollandiae). 1. Methods for collection of semen.

Two methods for collecting semen from male emus using an artificial cloaca (AC) have been developed. In the first method, the male mounts the female teaser and the collector effects erection and subsequent ejaculation using the AC. The second method takes advantage of the development of sexual behaviour directed towards the semen collector and semen is collected when the male mounts the collector's back. Eight of 11 males were successfully trained with teasers and 5 of the 7 males trained without teasers ejaculated successfully. The ease of training varied between birds. The use of a teaser was very valuable, as the crouching behavior of the teaser elicited mating attempts in every male. The training and collection of semen was done by one person. Both methods can be used for routine collection of semen, as they take advantage of natural stimulation and the voluntary ejaculation reflex to which the birds adapted readily.

Animals↗