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Timing of sperm transport, sperm penetration and cleavage in the rat.

Times of sperm entry into the oviduct from the uterus, into the ampulla from the isthmus; of sperm penetration into oocytes, and of cleavage, were determined using three mating regions. Time intervals and their errors of estimation were calculated. Spermatozoa were first found in the isthmus of the oviduct no earlier than 15 minutes after coitus, but required four hours to ascend the oviduct to the ampulla. The rate of sperm arrival was equal to the rate of sperm penetration, i.e., about 3 sperms/hour. Time of cleavage in vivo was 20.6 hours after sperm penetration in ad libitum mated animals. In culture, oocytes cleaved at exactly the same time as in vivo. Delaying sperm arrival to the site of fertilization (by delaying mating) shortened the time interval between median time of sperm penetration and median time of cleavage. It was concluded that the time of cleavage of the oocyte reflects primarily the time of sperm penetration, but is also influenced by the postovulatory age of the oocyte.

Animals

Facilitative and inhibitory influences of reproductive behavior on sperm transport in rats.

Six experiments were performed to investigate the effects of the rat's copulatory behavior on sperm transport in the female's reproductive tract. Data showed that (a) transcervical sperm transport in rats requires 6--10 min after ejaculation for completion; (b) transcervical transport of large numbers of sperm requires that the vaginal plug remain lodged tightly in the vaginal-cervical junction; (c) maintenance of an immobile posture by the male, and possibly by the female, at ejaculation facilitates the deposition of a tightly lodged vaginal plug and the transport of large numbers of sperm through the cervix; (d) a single intromission occurring within 2 min after ejaculation disrupts sperm transport, but more copulatory stimulation is required to disrupt sperm transport when delivered between 4 and 10 min after ejaculation; and (e) the average postejaculatory interval is long enough to prevent a male from disrupting the transport of most of his own sperm from the preceding ejaculation.

Animals

Species differences in contractility of seminiferous tubules and tunica albuginea as related to sperm transport through the testis.

Frequency and depth of contractions and tonus--i.e., diameter of the tubule or shift of the baseline for the capsule--of both the seminiferous tubules and the tunica albuginea were quantified for rat, mouse, rabbit, hamster and ground squirrel tests. In the ground squirrel, contractility was measured prior to, during and after breeding. The rat testes had the strongest tubular contractions; those of the mouse, squirrel and rabbit exhibited intermediate values, and the hamster tests had the weakest tubular contractions. The rabbit tests exhibited the strongest, most well-developed rhythmical capsular contractions while the rat, mouse, hamster and squirrel tests showed no definite rhythmical contractions. Hamster tests apparently depend primarily upon fluid secretion by the seminiferous tubules for sperm transport through the tests to the epididymis, while the squirrel, rat and mouse tests utilize both fluid secretion and some tubular contractions. The rat apparently utilizes tubular contractions more so than the other rodents studied for sperm transport.

Animals

Hormonal control of seminiferous tubule contractions. A hypothesis of sperm transport from the testicle.

The effects of steroids on the presence or absence and relative magnitude of rat seminiferous tubule contractions were evaluated microscopically. Both 10- and 30-mg implants of estradiol in vivo and concentrations of 10(-8) or 10(-9) M estradiol in vitro depressed the percentage of seminiferous tubules contracting without altering the magnitude of the contraction. Higher doses of both testosterone and dihydrotestosterone in vivo and in vitro maintained the tubular contractions at normal or above normal levels whereas lower doses of these compounds reduced both the percentage and magnitude of the tubules contracting. The results from these experiments suggest that rat seminiferous tubule contractions can be altered by steroids. Testosterone and dihydrotestosterone inhibit the contractions at lower doses and stimulate the contractions at higher doses and thus may regulate the transport of spermatozoa from the rat testicle.

Animals

[Effect of coitus on sperm transport and fertilization in rabbits].

The number of spermatozoa into the Fallopian tubes and levels of in vivo fertilization were measured following different treatment. The results show that copulation by the artificially inseminated animal has a strong influence on the transport of the rabbit spermatozoa and "in vitro" fertilization. This constitutes some more evidence about the physiological role played by the utero-tubal junction.

Animals

The survival and transport to the site of fertilization of diploid rabbit spermatozoa.

The possible involvement of diploid spermatozoa in the production of triploid zygotes in the rabbit has been investigated in terms of the success of diploids relative to haploids in reaching the site of fertilization, with special reference to any possible selectivity of sperm transport within the female tract. The observed large significant reduction in the incidence of diploid spermatozoa between the ejaculate and the oviducts would greatly reduce the chances of, but not necessarily prevent, a diploid spermatozoon fertilizing an egg. This reduction appears to be due to a combination of the reduced survival of diploids in the female tract and a selectivity of sperm transport dependent on sperm motility.

Animals