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Query: UMLS:C0016382 (flushing)
 6,387 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

Follicular oocytes (n = 81) collected from cattle at a local slaughterhouse were matured and fertilized in vitro. Of 27 ova 19 (70%) were penetrated by spermatozoa and 40/54 (74%) inseminated ova transferred surgically to the oviducts of a synchronized heifer were recovered by non-surgical flushing of the uterine horns 6 days later. Of the 40 ova 15 (38%) were at the morula, early blastocyst or diminutive morula stages. Culture in vitro sustained further development of all embryos and 9 were expanding or expanded blastocysts. One pregnancy resulted from non-surgical transfer of 2 blastocysts. The results demonstrate that immature oocytes from cattle can be matured and fertilized in vitro, subsequently develop to the blastocyst stage, and develop into a normal pregnancy after non-surgical transfer.
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PMID:Pregnancy resulting from cattle oocytes matured and fertilized in vitro. 343 Apr 67

Flushing the vasa deferentia (ductus deferentes) at the time of vasectomy reduced to zero the number of intact spermatozoa by postvasectomy day 6 in the dog and by postvasectomy day 7 in the cat and shortened the time from vasectomy to azoospermia in the dog, but not in the cat. The fluid used to flush the vasa deferentia was not eliminated through the penile urethra, but flowed into the urinary bladder, indicating that the least resistant pathway for the exit of vasal content in the anesthetized dog and cat is toward the urinary bladder. Both control and treated dogs and cats had spermatozoa in the urine obtained by cystocentesis immediately after ejaculation or ejaculation and flushing of the vasa deferentia. Flushing the vasa deferentia at the time of vasectomy is easy to do, safe, and can be used in clinical practice to decrease the time from vasectomy to the safe utilization of dogs and cats as teasers. The procedure has potential application to males of other species.
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PMID:Effect of flushing the vasa deferentia at the time of vasectomy on the rate of clearance of spermatozoa from the ejaculates of dogs and cats. 395 37

Spermatozoa were recovered from the isthmus of the rabbit oviduct at 4 and 11 h post coitum using several defined flushing media. The motility of spermatozoa in the isthmic flushings was subsequently analysed from video recordings. There was little sperm movement in the native isthmic fluid, but vigorous flagellar activity and hyperactivated movement were induced by flushing the isthmus with 0.25 M-sucrose, apparently an effect of dilution. Flushing with a complex culture medium resulted in similar stimulation of sperm movement. When pyruvate was present in the medium, hyperactivated flagellar bending was stimulated, whereas these movements were virtually absent when glucose alone was present. The stimulating effect of dilution was less pronounced when the flushing medium contained 50 mM-potassium. When the isthmus was flushed with media containing 50 mM-K+ and the K+ concentration was lowered to 5 mM during a washing procedure, large-amplitude flagellar movements were sequentially suppressed and restored. The restoration of large-amplitude movements was enhanced when pyruvate was present in the 5 mM-K+ washing medium. These results suggest that alterations in the concentration of both K+ and pyruvate may have a role in regulating the motility of rabbit spermatozoa in the oviducal isthmus, K+ being inhibitory and pyruvate stimulatory.
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PMID:A possible role for potassium and pyruvate in the modulation of sperm motility in the rabbit oviducal isthmus. 654 Mar 6

A total of 23 mares were inseminated once within 0-6 h after clinical detection of ovulation, 14 with fresh and 9 with deep-frozen semen containing 0.1 x 10(9) to 4.7 x 10(9) motile spermatozoa. Within these two groups, the mares were slaughtered 2, 4 or 6 h after insemination and their genital tracts removed. The utero-tubal junction, isthmus and ampulla ipsilateral to the ovary in which ovulation occurred were flushed separately for sperm recovery. In 1 or 2 mares of each group, the uterine horn and corpus uteri, the cervix and vagina were also flushed. Tissue samples were collected from the contralateral oviduct and the other genital regions and prepared for scanning electron microscopy to show spermatozoa distribution in situ. Flushings were also prepared for scanning electron microscopy. There were no significant differences in the extent of sperm migration and in the number of spermatozoa in the different regions of the oviduct 2, 4 or 6 h after insemination of fresh or frozen semen. There was, however, a striking difference in sperm number within the time intervals examined; the numbers were greatest at 4 h after insemination. SEM of spermatozoa in the various regions of the oviducts failed to indicate any alterations to the sperm-head membranes that could be associated with sperm capacitation. The majority of spermatozoa found in the uterotubal junction, isthmus and ampulla showed morphological integrity.
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PMID:An investigation of sperm migration into the oviducts of the mare. 696

Spermatozoa were recovered from the ejaculate, vagina, uteri and oviducts of mated does between 2.5 and 14 h p.c. For each sample, the proportion of spermatozoa exhibiting no binding of IgG from normal serum, after air drying and acetone fixation, was compared with the proportion of acrosomeless spermatozoa as assessed by staining with eosin and fast green. The correlation was excellent (r = 0.97; P less than 0.001) suggesting that failure of acetone-fixed spermatozoa to bind IgG from normal serum may reflect acrosome absence rather than 'acrosomal uncoatibility'. Usually the proportion of immunofluorescence negative or acrosomeless spermatozoa was about 10% in the ejaculate; 15% in the vagina; 25% in the uterus and 70-100% in the oviducts. This phenomenon is not an air-drying artefact, and seems to be independent of flushing medium.
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PMID:Equivalence of 'non-IgG binding' and 'acrosomeless' sperm populations from the female genital tract of the rabbit. 703 26

Some data on the synthesis and characterization of poly(HEMA-MAC) and its applications for fertility control are presented. This new technique involves the use of the polymer, which when injected into the vas deferens lowers the pH sufficiently so as to kill the spermatozoa passing through. The polymer provides an acidic environment for a prolonged time and slowly erodes. The fertility may be restored after complete solubility of the polymer itself over a period of time or by flushing it with a suitable solvent. It is a nonsurgical, nonocclusive, and reversible method of male contraception. In regard to the experimental procedure, copolymerization of HEMA with MAC (35% by weight) in methanol was carried out in a nitrogen atmosphere in glass ampules. Irradiation was performed in a cobalt-60 radiation chamber. All the samples were irradiated at a dose rate of 130 rad/s for a total dose of 0.936 Mrad at room temperature. For studying the spermicidal actions of the copolymer, epididymal fluid from the male rat was collected, diluted 1:10 with Ringer-fructose buffer and microscopically examined. Small swollen pieces of poly(HEMA-MAC) copolymer as well as poly(HEMA) homopolymer were then added to the epididymal fluid and the effect on the spermatozoa was noted. The spermicidal action "in vitro" was indicated by the loss of motility of the spermatozoa immediately on coming in contact with the poly(HEMA-MAC). The spermatozoa remained immotile even after the removal of the copolymer, indicating that they were dead. The polymer treated spermatozoa did not take up any supravital stain confirming that they were killed. This effect was absent only when poly(HEMA) was used. These results clearly show that the spermicidal activity is mainly due to the carboxylic groups of MAC. Possibly the low pH environment due to the ionization of carboxylic groups is responsible for killing the spermatozoa. For all the experiments the injection of the polymeric solution into the vas deferens was given only by exposing the vas deferens, but it is reported that in humans injection into the scrotal wall is possible. The new technique has all the characteristics which can lead to an ideal contraceptive method. Preliminary results of "in vitro" experiments on human spermatozoa with these hydrogels are encouraging.
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PMID:Novel mode of contraception using polymeric hydrogels. I. 705 60

Of 14 lactating opossums maintained in laboratory conditions, 13 mated 4.7-8.5 days after removal of pouch young. The time between this removal and onset of receptive oestrus was negatively correlated with the age of the pouch young. Mating generally occurred between 24:00 and 06:00 h, with ovulation following between 13:00 and 16:00 h. Each animal ovulated a mean of 29.6 eggs (range 19-40), approximately equal numbers coming from both ovaries. Spermatozoa were absent from the uterus and were present only in the oviducts during the periovular period. Those not cleared by flushing (1-160 x 103/oviduct) remained incarcerated in isthmic crypts lined by a simple cuboidal epithelium. Spermatozoa in crypts were paired, separating or single. The progressively motile cells flushed from the oviduct presented a similar pattern to that in the crypts, about 30% of spermatozoa were firmly paired, the others either loosely associated or single. Only single spermatozoa attached to ova. Monospermic fertilization followed shortly after ovulation, and no supplementary spermatozoa were present in the perivitelline space. Deposition of the mucoid layer on the zona pellucida then began, often before incorporation of the fertilizing spermatozoon by the vitellus was complete. The oviducal epithelium was formed throughout by ciliated and secretory cells. In the ampulla and upper isthmus, the secretory cells produced the mucoid material which formed a thick coat over the egg surface. Ovum transit through the oviduct was rapid, in one animal eggs had reached the uterus and acquired a shell within 15-20 h of ovulation.
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PMID:Induction of oestrus, recovery of gametes, and the timing of fertilization events in the opossum, Didelphis virginiana. 719 86

The ability of Synthetic Oviductal Fluid (SOF) and Minimum Essential Medium (MEM) to support sperm binding, sperm penetration and subsequent cell division of ovine tubal oocytes in vitro was evaluated. These media contained no protein, 3% (w/w) bovine serum albumin (BSA) or 20% (v/v) lamb serum (LS). Midventral laparotomies were performed on 49 ewes synchronized with progesterone and then superovulated, and tubal oocytes were collected by flushing the oviducts. Oocytes were pooled and randomly added to 2 X 10(7) ejaculated spermatozoa in 1 ml of treatment media that had been preincubated in tubes for 3 hr at 37 C under 5% CO2 in air. After an additional 3 hr of culture in a rotating tissue culture drum, oocytes were further cultured in microdrops of the same medium for 48 hr and observed for sperm penetration, cell division and fragmentation. Oocytes were then stained with aceto-orcein and observed for penetration, multiple nuclei and bound sperm. Percentage of oocytes showing penetration in SOF, SOF+ BSA, SOF+LS, MEM, MEM+BSA and MEM+LS was 14, 3.6, 7.8, 11.1, 8.7 and 12.8, respectively; percentage of oocytes cleaving was 8, 3.6, 5.9, 4.4, 4.3 and 4.3; percentage of oocytes fragmenting was 40, 60, 60.8, 20, 60.9 and 29.8, and the average number of sperm cells bound per oocyte was 82, 177, 117, 41, 56 and 47. No cell division was observed for control oocytes (no sperm added), but 72.7, 80 and 76.9% fragmented in SOF, SOF+BSA and SOF+LS, respectively. No difference was found among the media in their ability to support sperm penetration and subsequent cell division in vitro. All media tested supported a high incidence of sperm binding and oocyte fragmentation.
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PMID:Influence of culture media on in vitro fertilization of ovine tubal oocytes. 744 Apr 50

This study aimed to determine the number and distribution of spermatozoa within the human Fallopian tubes around ovulation. Parous women, undergoing total abdominal hysterectomy for menorrhagia, were inseminated with either partner's semen (3/10) or donor semen (7/10). Approximately 18 h later both Fallopian tubes were ligatured into ampullary, isthmic and intramural regions. These were removed and assessed for sperm content by flushing, scanning electron microscopy (SEM) or homogenization. A median of 251 spermatozoa were recovered (range, 79-1386). The number of spermatozoa within each tube was not significantly different. The ovulatory ampulla contained a significantly (P < or = 0.01) larger percentage of spermatozoa than the non-ovulatory ampulla. The number of motile spermatozoa inseminated was not significantly correlated to the number of spermatozoa recovered, but a trend was identified. The time between the onset of the luteinizing hormone surge and hysterectomy was significantly correlated (P < or = 0.01) to the number of spermatozoa within the intramural regions, but not to the tubal sperm distribution. Spermatozoa were not observed, by SEM, bound to the tubal epithelium. These data suggest that, after artificial insemination at least, sperm access to the human Fallopian tube may be controlled, but that ovulation does not affect the redistribution of spermatozoa between tubal regions and that the isthmus does not appear to act specifically as a sperm reservoir.
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PMID:Sperm numbers and distribution within the human fallopian tube around ovulation. 815 Aug 97

The process of sperm transport from the cervix, where a leukocytic reaction is initiated, through the uterus to gain access to the site of fertilization is very poorly understood. This preliminary study was designed to utilize a uterine flushing technique to determine firstly, the number of spermatozoa that can be recovered from the uterine cavity at 4 h post-insemination, around the time of ovulation, and secondly, to establish whether the spermatozoa initiate a leukocytic response while present. Uterine flushing was carried out in 10 potentially fertile women at 4 h post-insemination with donor semen, 24-36 h after the onset of the luteinizing hormone (LH) surge. The flush fluid was analysed for the numbers of spermatozoa and leukocytes present. In 8/10 women spermatozoa were retrieved from the uterus, in consistently low numbers (median 46, range 3-415). In 5/5 women leukocytes were recovered (median, 2.75 x 10(8)/l, range 2.0 x 10(8)-12.7 x 10(8)/l) from an origin other than peripheral blood contamination. These results suggest firstly that the flushing technique was a consistent method for retrieving spermatozoa and leukocytes from the uterine cavity, secondly that only low numbers of spermatozoa can be retrieved on flushing and thirdly that the leukocytic reaction to spermatozoa extends to the uterine cavity.
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PMID:Uterine flushing: a method to recover spermatozoa and leukocytes. 834 87


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