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At least 1,099 records · Page 61Linked to original sources
PubMed1994

Copper in split and daily ejaculates.

The authors studied the copper level in three splits of 21 ejaculates to locate the origin of copper in semen. The copper level was rich in the first split and poor in the second. The results indicated that copper is released from all portions of the genital tract and that the major share is from the prostate gland. Another group of 26 volunteers submitted their semen samples once a day for 10 days for a study of the role of copper in fertility. A gradual increase in sperm motility was observed from the first day. There was no consistency in the level of copper in this study, and it did not correlate with any of the semen parameters studied.

Adult↗
PubMedDate not supplied

Leukocytic infiltration into the human ejaculate and its association with semen quality, oxidative stress, and sperm function.

Immunocytochemical techniques have been used to monitor the size and composition of the leukocyte population in unfractionated human semen samples and sperm populations generated by Percoll gradient centrifugation. The characteristics of the leukocyte population have then been related to the quality of the semen profile, the production of reactive oxygen species, and the functional competence of the spermatozoa. A majority (97%) of the ejaculates examined contained leukocytes, and in 82.4% the major cell type was the granulocyte. Small numbers of T cells, B cells, and monocytes/macrophages could also be found in 62%, 43%, and 21% of samples, respectively, and patients were occasionally identified in whom one of these cell types became the predominant leukocyte species. Although a subpopulation of patients was identified in whom the infiltration of multiple leukocyte species was positively correlated with the concentrations of spermatozoa and precursor germ cells in semen, in general, the presence of leukocytes, to the point of leukocytospermia, did not significantly influence any component of the semen profile. Similarly, the fertilizing potential of the washed spermatozoa, as assessed by in vitro tests of the acrosome reaction and sperm-oocyte fusion, was not correlated with the concentration of seminal leukocytes. In contrast, the carryover of leukocytes into the washed sperm preparations profoundly influenced the fertilizing potential of the spermatozoa via mechanisms that were associated with the production of reactive oxygen species. These results have implications for the diagnostic significance of leukocyte contamination in the context of male infertility and assisted conception.

Cell Movement↗
PubMedDate not supplied

[The dynamics of the species composition and antilysozymal activity of ejaculate microflora under the action of local hyperthermia].

Changes in the antilysozyme activity of bacteria under the action of high temperature and short-wave hyperthermia have been studied. The regulating influence of these factors on the species composition and persistence characteristics of the microflora of ejaculate obtained from sterile patients has been demonstrated. A method for the treatment of male sterility is proposed.

Adult↗
PubMed1996

[Modification of the quality indicators of the ejaculate of beagle dogs due to frequent collections over time].

Ejaculates from five adult beagle dogs were investigated for changes of spermatologic parameters. Semen was collected daily during 12 weeks. The parameters volume, sperm count, and transmigration rate (TMR) increased during the first three to five weeks and decreased in the middle of the experiment. The percentage of morphologically abnormal spermatozoa just exceeded 20% from the fifth to the seventh week and in the tenth week, respectively. Either the results remained on a low level (volume), or they returned to normal from the tenth week on (morphology, TMR, sperm count). Semen quality diminished after five weeks. It is concluded, that daily semen collections during more than five weeks can cause decreased libido, aspermia, and impairment of the conception rates.

Animals↗
PubMed1997

Pregnancies from imipramine and xylazine-induced ex copula ejaculation in a disabled stallion.

Breeding or semen collection was attempted using: natural cover, manual stimulation, artificial vagina, pharmacologic induction of ejaculation, and electroejaculation. Sperm cells were recovered from the ductus deferens and epididymides post mortem. Only semen collected ex copula by imipramine and xylazine treatment resulted in conceptions (4/5). This is the first report of pregnancies in horses from ex copula semen collection.

Animals↗
PubMedDate not supplied

[The enzymatic activity of the seminal plasma in ejaculates of different fertilities].

Enzymatic ejaculates activity was studied in 15 fertile and 65 subfertile samples of human sperm. The activity of alkaline phosphatase (EC 3.1.3.1), alpha-amylase (EC 3.2.1.1), gamma-glutamyl transferase (EC 2.3.2.2), creatine kinase (EC 2.7.3.2), total lactate dehydrogenase (EC 1.1.1.27) and lactate dehydrogenase-1 was compared to spermogram findings according to 14 morphological and physicochemical criteria of fertility. The enzyme activity depends on functioning of the testes, seminal vesiculae, prostate, bulbourethral glands and is involved in formation of fertility. The findings allowed elucidation of the role of synthesis and some function of spermoplasma enzymes. Practical applications of the above data are discussed in the treatment of male infertility and to raise fertilizing power of the sperm in artificial insemination.

Adult↗
PubMedDate not supplied

[The immunochemical determination of the concentration of organ-specific ejaculate proteins in the differential diagnosis of chronic inflammatory diseases of the male reproductive system].

Concentrations of lactoferrin (LF), alpha-microglobulin of fertility (AMGF) and specific thermostable alpha-glycoprotein (STAG) which are markers of the prostate, seminal vesicles and testiculi in ejaculate, respectively, were determined by Ouchterlony's immunodiffusion method in 148 patients with chronic prostatitis (group 1), 26 patients with combination of prostatitis with chronic epididymitis (group 2) and 22 healthy controls (group 3). After that the patients were given prostatilen. It was found that high pretreatment values of LF registered in groups 1 and 2 lowered close to those in the controls. This shows elevated LF to be a diagnostic sign of prostatitis. In group 1 AMGF was lower than in controls, in groups 1, 2 and 3 STAG levels were similar.

Adult↗
PubMed1998

Evidence based assessment of rapid ejaculation.

This manuscript reviews the clinical and scientific methods utilized to assess treatment outcome in rapid ejaculation. The current methods and measures are critically evaluated and suggestions for future research efforts are included.

Ejaculation↗
PubMed1987

Effects of dibromochloropropane and ethylene dibromide on biochemical events and ultramorphology of ejaculated ram spermatozoa in vitro.

The effects of dibromochloropropane (DBCP) and ethylene dibromide (EDB) on the function and ultrastructure of freshly ejaculated washed ram spermatozoa were assessed. These two compounds inhibited the collective motility of the sperm in a dose-dependent fashion when the sperm cells generated their energy either by mitochondrial respiration (2-deoxyglucose-treated sperm cells) or by the intact energy production system. DBCP and EDB inhibited the oxygen uptake by the sperm in a dose-dependent manner. No change in lactic acid accumulation and glucose utilization by the sperm cells was noted following DBCP and EDB addition. No change in the collective motility of the sperm was noted when DBCP or EDB were added to spermatozoa treated with the electron transfer inhibitor, antimycin A. Electron microscopy studies of sperm cells treated with DBCP revealed lesions in the plasma membrane adjacent to the acrosome and in the acrosomal membrane forming vesiculations. The inner membrane and the matrix space of the mitochondria were condensed following DBCP treatment, leaving a large mitochondrial peripheral space, compared with the control. EDB, at the concentration studied, caused no change in the ultramorphological structure of the sperm. DBCP was more potent, at least 4-fold, compared with EDB. An in vitro direct effect of DBCP and EDB on ram spermatozoa was established. It is suggested that quantitative measurements of sperm collective motility derived by different metabolic pathways can be used as an in vitro toxicological model for evaluation of toxicological and environmental factors affecting biological systems.

Animals↗
PubMed1978

Identification of ejaculate derived propylamine found in collagen sponge contraceptives.

Propylamine is identified as one of the compounds present in odoriferous intravaginal contraceptive sponges from sexually active women. This compound also appears in samples of human ejaculate incubated at 37 degrees C for seven days. We have identified propylamine by gas liquid chromatography, mass spectroscopy and as N-propylbenzoylamide. Evidently the compound forms enzymatically from spermine and spermidine. We believe that this is the first time that propylamine has been identified as forming from human tissue.

Collagen↗
PubMedDate not supplied

Ureteral ejaculation of urine visualized by ultrasound.

This article describes an ultrasonographic noninvasive method for the visualization of the ureteral ejaculation of urine into the bladder and its use in 99 normal women and in one affected by a previously unsuspected bilateral hydronephrosis and hydroureter.

Female↗
PubMed1989

Induction of the acrosome reaction in ejaculated goat spermatozoa by preincubation in chemically defined medium.

The aim of the present study was to examine the effects of the elimination of energy substrate from the medium and the effects of the preincubation vessel, temperature, and time on the induction of the acrosome reaction in ejaculated goat spermatozoa in chemically defined medium. Washed spermatozoa were resuspended in Brackett-Oliphant (BO) medium or substrate-free BO medium to give a high concentration and preincubated in open test tubes or sealed glass tubes at 37.0 or 39.5 degrees C for 1, 2, or 3 h. Sperm acrosome reaction was evaluated using a simplified triple-stain technique and a hamster test. It was found that the goat sperm acrosome reaction occurred more readily in the sealed glass tubes than in open test tubes, in substrate-free BO medium than in BO medium, and at 39.5 than at 37.0 degrees C. During preincubation with substrate-free BO medium in sealed glass tubes at 39.5 degrees C, the optimum time necessary to induce the acrosome reaction in goat spermatozoa was 2-3 h.

Acrosome↗
PubMed1988

Characterization of actin isoforms in ejaculated boar spermatozoa.

Actin was localized in boar ejaculated spermatozoa by using specific antisera against cytoplasmic isoforms of actin [Otey et al., J Cell Biol, 102:1726-1737, 1986; Skalli et al., J Cell Biol, 103:2787-2796, 1986; Miller et al., Biochemistry, 26:6064-6070, 1987]. Indirect immunofluorescence and immunoelectron microscopy showed that gamma and beta actins were codistributed in the acrosomal and postacrosomal regions. Sperm actin was also identified on two-dimensional gel as two spots in the isoelectric point and molecular weight corresponding to beta and gamma actins. Coelectrophoresis of sperm actin and chicken gizzard actin and immunoblots stained with the specific antibodies confirmed the presence of these two isoforms of actin.

Actins↗
PubMed2005

Ejaculates from the common marmoset (Callithrix jacchus) contain semenogelin and beta-microseminoprotein but not prostate-specific antigen.

Human seminal plasma contains high concentrations of prostatic acid phosphatase (PAP), prostate-specific antigen (PSA), beta-microseminoprotein (MSP), semenogelin I (SgI), and semenogelin II (SgII), whereas only PAP and MSP are present in rodents. In order to gain a better understanding of the evolution and function of semen proteins, we have studied ejaculates from the common marmoset (Callithrix jacchus)-a New World monkey. Semen samples were analyzed with SDS-PAGE, Western blotting, and isoelectric focusing. Under reducing conditions the dominating protein components appear as heterogeneous material of 55-70 kDa and distinct protein bands of 85, 17, 16, and 15 kDa. The heterogeneous material contains glycosylated material detected by an antiserum recognizing both human SgI and SgII. Southern blotting indicates that the common marmoset has genes for both SgI and SgII. There are several marmoset MSP genes, but the strong immunoreactivity against one 15 kDa semen component with pI 7.3 suggests preferential expression of one gene in the prostate. Expression of two other genes cannot be excluded as indicated by weak reaction to isoforms with pI 6.6 and 4.9. Unexpectedly, PSA was not detected by either immunological methods or activity measurements. This is in agreement with results from Southern blotting suggesting that the common marmoset might not have a PSA gene. Thus, in this study we have shown that semen coagulum proteins are present in marmoset seminal plasma, but the lack of PSA precludes a similar liquefaction as of human semen.

Animals↗
PubMed1998

Temporal manipulation of ejaculate components by newly fertilized Drosophila melanogaster females.

Observations of newly mated Drosophila melanogaster females suggest that females control the times at which components of the ejaculate cause behavioural and physiological changes characteristic of fertilized females. Females that were assayed immediately after they mated elicited as much courtship as they did when they were virgins, but were unreceptive to copulation. Within a few minutes of when they disengaged from copulation, most females performed ovipositor extrusion, which has been classified as a rejection behaviour, in response to courting males or males that had previously performed courtship. Most females that were assayed immediately after mating had already ovulated. The females, however, do not begin to lay eggs until 4-6 h after mating, at which time they elicit very little courtship (Scott & Richmond 1985, Anim. Behav., 33, 817-824). Our observations suggest that neither ovipositor extrusion nor male-synthesized pheromones that are transferred to females' cuticles during copulation inhibit males' courtship of newly fertilized females. Thus, males cannot determine that newly fertilized females are unreceptive to copulation. These observations also indicate that the failure of newly fertilized females to mate with males is not a consequence of the females' inability to elicit vigorous courtship. Copyright 1998 The Association for the Study of Animal Behaviour. Copyright 1998 The Association for the Study of Animal Behaviour.

Journal Article↗
PubMed1999

In vitro comparison of fowl sperm viability in ejaculates frozen by three different techniques and relationship with subsequent fertility in vivo.

A series of experiments was conducted to compare the viability of fresh fowl spermatozoa, samples suspended in three cryoprotectants (CPAs), frozen/thawed samples, and frozen/thawed samples maintained in vitro for up to 24 h. The CPAs used were glycerol (Glyc), dimethylacetamide (DMA), and dimethylformamide (DMF). Viability was assayed using two double stains, Eosin + Nigrosin or SYBR-14 + PI (propidium iodide). Semen samples examined with SYBR-14 + PI indicated significant differences in viability between fresh and ready-to-freeze preparations (fresh, 83%; Glyc, 73%; DMA, 74%; DMF, 72%; P < 0.05). In contrast, Eosin + Nigrosin did not detect any difference at this stage (fresh, 88%; Glyc, 86%; DMA, 87%; DMF, 88%; P > 0.05). The percentages of viable spermatozoa in frozen/thawed ejaculates stored in vitro for 0, 4, and 24 h were generally higher in samples treated with glycerol than in those treated with DMA or DMF, irrespective of the technique used to assess sperm viability (P < 0.05). Fertility in eggs obtained from hens inseminated with semen frozen in DMA reached levels comparable to those obtained from hens inseminated with fresh undiluted semen (88 and 93%, respectively; P > 0.05). In contrast, fertility of eggs from hens inseminated with semen frozen in DMF or glycerol was significantly lower, although still very good, than that observed in eggs from hens inseminated with semen frozen/thawed in DMA (79 and 76%, respectively; P < 0.05). Finally, the double stain SYBR-14 + PI was proven more effective than Eosin + Nigrosin to assess sperm viability in fresh, stored, and frozen fowl semen. However, additional tests (e.g., morphology, acrosomal status, motility) remain necessary to develop a working model of in vitro sperm analysis capable of revealing the fertilizing potential of fresh and frozen fowl spermatozoa.

Acetamides↗
PubMed1978

DNA repair processes in germ cells demonstrated in ejaculated sperms of rabbits treated with methyl methane sulfonate.

Male rabbits were treated with a single i.v. injection of 22.5 mg/kg methyl methane sulfonate (MMS). 0--24 h later [3H]-thymidine was injected in both testicles. Incorporation of the isotope in germ cell DNA was demonstrated in ejaculated sperms. In controls labeled sperms were demonstrated first on day 40--43. These cells were in the preleptotene spermatocyte phase at the time of [3H]-thmidine injection. In rabbits treated with MMS significant radioactivity occurred in sperms collected from day 19 onwards. These cells were in late spermatocyte and early spermatid phase of maturation when [3H]-thymidine was injected. Incorporation of thymidine in these cell populations is interpreted as an expression of unscheduled DNA synthesis, a repair process initiated after chemical damage of germ cell DNA by MMS. The usefulness of the rabbit test system within the framework of conventional mutagenicity screening tests is discussed.

Animals↗