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Query: UMLS:C0432222 (SEM)
 47,337 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

Seminal (i prolactin) immunoreactive prolactin was studied in 14 healthy subjects, ages 31 + or - 2 SEM, before and after undergoing elective vasectomy for birth control. Seminal plasma was separated within 2 hours of ejaculation, and prolactin was measured in duplicate by radioimmunoassay. The difference between the prevasectomy (mean + or - SEM 11.1 + or - 0.8 ng/ml) and postvasectomy seminal i prolactin (mean + or - SEM 9.9 + or - 0.7 ng/ml) was statistically significant (mean + or - SEM 1.21 + or - 0.53 ng/ml, paired t-test, t=2.36, P 0.05). The mean prevasectomy seminal prolactin correlated with the corresponding mean postvasectomy value of the same subject (linear regression analyses, r=0.77, P 0.001). This study suggested that the accessory sex organs were the major source of seminal immunoreactive prolactin, and that a minor contribution might come from the in vivo presence of spermatozoa and/or testicular secretions. It also suggested that the magnitude of seminal immunoreactive prolactin was characteristic for each individual.
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PMID:Inherent ranges of seminal prolactin in pre- and postvasectomy subjects. 4 2

Samples of human semen frozen in liquid nitrogen ( - 196 degrees C) with no glycerol, 5 and 10% glycerol were compared with samples that were untreated, with 10% glycerol but not frozen, and spermatozoa frozen at -20 degrees C. SEM and TEM of the samples indicates that 10% glycerol caused fewer surface changes of the spermatozoa than other treatments. Motility counts after the various freezing treatments were also highest when 10% glycerol was used as the cryoprotectant. Nonetheless, cryopreservation is detrimental to spermatozoa and often causes considerable damage to the acrosome with a leakage of the acrosomal contents.
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PMID:Surface structure of spermatozoa frozen for artificial insemination. 88 75

This study compared swim-up and Percoll preparation of fresh semen samples for in-vitro fertilization. Sixty trials of in-vitro fertilization (IVF), 38 with normal semen and 22 with abnormal semen, comprising 734 oocytes were included in the study. Each semen sample was prepared by both a swim-up technique and a simplified discontinuous (50%, 70%, 90%) Percoll gradient. The oocytes for each trial were distributed at random between the two sperm preparations and incubated with the same number of motile spermatozoa. Percoll gradient preparation produced a significantly higher final concentration of spermatozoa than swim-up preparation (mean +/- SEM: 6.6 +/- 1.5 x 10(6)/ml versus 1.9 +/- 0.2 x 10(6)/ml; P less than 0.01) but a significantly lower sperm motility (69 +/- 2% versus 94 +/- 1%; P less than 0.001) and a lower number of normal forms (55 +/- 2% versus 64 +/- 2%; P less than 0.01). The ability of the Percoll gradient method to extract motile spermatozoa was higher than that of the swim-up technique (20 +/- 15.6% versus 0.8 +/- 13.6%). Nevertheless, the rates of fertilization (61%), fertilization failure (18%) and polyspermia (9%), embryo quality evaluated by mean embryo scores (3.8 +/- 0.3) and the mean number of spare embryos frozen per trial (1.4 +/- 0.3) were strictly identical in both groups. The 24 pregnancies (including three from frozen--thawed embryos) obtained in these 60 trials (40% per oocyte retrieval) could not be separated according to the sperm preparation method, as embryos from both groups were replaced together.(ABSTRACT TRUNCATED AT 250 WORDS)
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PMID:Comparative auto-controlled study between swim-up and Percoll preparation of fresh semen samples for in-vitro fertilization. 131 14

Acetylcarnitine (AC), present in human spermatozoa and seminal fluid, plays an important role in sperm metabolism. To further investigate the effect of AC on sperm quality, AC (4 g/day) was given to 20 patients with idiopathic oliogasthenospermia for 60 days. AC had no effects on sperm density and total motility, but it did significantly increase progressive sperm motility (mean +/- SEM: 21.7 +/- 3.2% vs 38.2 +/- 4.7). The increment in sperm motility was sustained ( > or = 40%) in 12 patients (mean increment 2.7 fold). This parameter returned to basal value 4 months after therapy discontinuation. Five pregnancies occurred during treatment and only 2 during the 4 months follow-up ensuing therapy discontinuation.
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PMID:Effect of acetylcarnitine treatment in oligoasthenospermic patients. 134 82

The contribution of the toxicity of glycerol-egg yolk-citrate (GEYC) cryopreservative medium to the loss of function of human spermatozoa during cryopreservation was determined by investigating the effect of mixing semen with the medium on sperm motility. The percentage of progressively motile spermatozoa, velocity (micron s-1) and lateral head displacement (micron) (mean +/- SEM, n = 28) were 55 +/- 4.1, 47 +/- 2.7, 4.4 +/- 0.2 and 32 +/- 3.8, 40 +/- 2.5, 3.6 +/- 0.25 and 15 +/- 2.5, 28 +/- 1.1, 2.8 +/- 0.15 in suspensions of washed spermatozoa prepared from fresh, GEYC-treated and frozen-thawed semen, respectively. The variables changed only slightly after incubation for 3 h. The toxicity of GEYC did not vary significantly between samples which survived the complete freeze-thaw cycle well or very poorly. The toxicity of GEYC is responsible for about 50% of the loss of progressively motile spermatozoa during the complete cryopreservation process, but has little effect on the quality of motility. Susceptibility to GEYC does not explain observed differences in the ability of semen samples to survive freezing.
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PMID:The contribution of the toxicity of a glycerol-egg yolk-citrate cryopreservative to the decline in human sperm motility during cryopreservation. 140 92

To investigate the fertility of men who remain oligozoospermic despite sex steroid suppression, the in-vitro fertilizing capacity of residual spermatozoa was assessed in 30 men receiving intramuscular testosterone enanthate (TE). Spermatozoa were prepared by either Percoll or repetitive centrifugation/washing. Although the mean (+/- SEM) pretreatment zona-free hamster oocyte penetration (HOP) rates were similar (59.4 +/- 10.1 and 63.8 +/- 10.8%), following the induction of oligozoospermia the Percoll-prepared spermatozoa exhibited a penetration rate (26.9 +/- 10.2%) which was markedly greater than that obtained for sperm prepared by repetitive washing (0 +/- 0%). In addition, the partners of two men exhibiting a HOP test with Percoll-prepared spermatozoa, conceived despite a sperm concentration of 3 x 10(6) ml-1 and a negative HOP test with spermatozoa prepared by repetitive washing. These results suggest that Percoll preparation optimizes the assessment of in-vitro sperm function and that the fertility of men with TE-induced severe oligozoospermia is suppressed but not abolished.
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PMID:Residual sperm function in oligozoospermia induced by testosterone enanthate administered as a potential steroid male contraceptive. 142

Roosters homozygous for the rose comb allele (R/R) are subfertile. Likewise, roosters bearing the dominant spermatozoal degeneration allele (Sd) are subfertile. The objective of the present research was to see whether these effects were cumulative. Domestic fowl were bred in order to obtain males representing the following genotypes: R/r+ sd+/sd+, R/r+ Sd/sd+, R/R sd+/sd+, and R/R Sd/sd+. Duplicate fertility trials were conducted with Single Comb White Leghorn hens. In each trial, ejaculates were pooled according to genotype. The insemination dose was 1 x 10(8) viable spermatozoa per hen, and eggs were collected over a 21-day interval following a single intravaginal insemination. Fertility over the 21-day period was 53 +/- 2.1 (SEM), 36 +/- 1.6, 21 +/- 2.1, and 11 +/- 1.2%, respectively. Therefore, the effect of homozygosity for the R allele and the presence of the Sd allele were cumulative in the depression of fertility.
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PMID:Analysis of the combined effect of the spermatozoal degeneration allele (Sd) and homozygosity of the rose comb allele (R) on the duration of fertility of roosters (Gallus domesticus). 143 82

The endometrium of an infertile patient with Kartagener's syndrome showed initial secretory phase characteristics at SEM, whereas TEM analysis demonstrated several alterations in the central and peripheral microtubular distribution in 87% of the cilia examined. Such aspects seemed appropriate for a normal implantation, but the ciliary immotility or dyskinesia could cause an altered flow of the endometrial secretions and compromise the upstream movement of the spermatozoa.
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PMID:Ultrastructural aspects of endometrial surface in Kartagener's syndrome. 173 4

Previous hemizona assay (HZA) results have illustrated a positive and significant correlation between the percentage of morphologically normal spermatozoa in the semen and the number of spermatozoa tightly bound to the zona pellucida. The present study was designed to evaluate the morphologic features using strict criteria of spermatozoa tightly bound to the zona pellucida. Semen samples of 4 normozoospermic and 11 teratozoospermic men were used to compare the percentage of normal spermatozoa in the semen with that found 1) after swim-up separation and 2) bound to the zona under HZA conditions. The mean (+/- SEM) % normal forms for normozoospermic men in semen, after swim-up and zona-bound spermatozoa were 21.5 +/- 1.6, 27.5 +/- 2.9, and 44.8 +/- 3.4, respectively. A significantly higher % of normal forms were found among zona-bound sperm compared to swim-up forms (p = 0.02) and seminal sperm (p = 0.02). The mean % of normal sperm forms present in semen, after swim-up and zona pellucida-binding for teratozoospermic men, were 3.7 +/- 0.9, 5.8 +/- 1.6 and 15.6 +/- 3.1, respectively. Significant differences existed between the % of normal sperm forms found in the swim-up and zona-bound spermatozoa (P = less than 0.01 and P = less than 0.0003, respectively) compared to the original ejaculates. Results indicate that a selective process against abnormal spermatozoa occurs at the site of the zona pellucida.(ABSTRACT TRUNCATED AT 250 WORDS)
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PMID:Sperm selection capacity of the human zona pellucida. 175 Oct 39

Ovulation rate and semen quality in French Angora rabbits were investigated to determine the potential of improving breeding practices in this breed. The proportion of does ovulating and their ovulation rate were studied in 40 females, as well as sexual behaviour and semen quality in 8 males. The experiments took place in autumn 1987 and were repeated in winter. Three groups of does were injected with 25, 50 IU hCG or 0.8 microgram GnRH (groups 1, 2 and 3, respectively). Another group was mated and served as a control (group 4). Hormonal treatments improved the proportion of does which ovulated (95, 90, 74 and 28% in groups 1-4, respectively; P less than 0.05) but did not change their ovulation rate (10.9 +/- 0.7, 10.7 +/- 0.7, 11.3 +/- 0.8 and 8.9 +/- 1.3 corpora lutea per ovulating female, groups 1-4, respectively; m +/- SEM, NS). In males, two ejaculates were collected twice weekly for 3.5 weeks from 8 bucks. Ejaculates obtained in March were better than those collected in November (volume: 0.33 vs 0.23 ml, P less than 0.01; raw motility: 5.2 vs 3.9, P less than 0.01; individual motility: 2.7 vs 2.1, P less than 0.05; number of living spermatozoa per ejaculate: 71 vs 28 x 10(6), P less than 0.01, respectively). These results suggest that artificial insemination may be utilized to improve reproductive performance in French Angora rabbits.
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PMID:[Reproduction of French Angora rabbits: ovulation in the female, semen production in the male]. 177 58


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