Male-induced oestrus and ovulation in female brush-tailed bettongs (Bettongia penicillata) suckling a young in the pouch

1994 ◽  
Vol 6 (4) ◽  
pp. 445 ◽  
Author(s):  
MJ Smith
Keyword(s):  
Corpus Luteum ◽  
Adult Male ◽  
Post Partum ◽  
Suckling Period ◽  
Vaginal Smears ◽  
Induced Ovulation ◽  
Unusual Condition ◽  
Bettongia Penicillata ◽  
To Come ◽  
Diapause Embryo

Female brush-tailed bettongs isolated from males usually do not come into oestrus or ovulate. Individuals isolated during pregnancy and at parturition do not ovulate post partum and are in the unusual condition for a macropodoid of suckling a pouch young but lacking a quiescent corpus luteum or a diapause embryo. Females in this condition were tested for their ability to come into oestrus and to ovulate after re-introduction to the male. When returned to the male on Day 1 of lactation, females generally mated before Day 2 and ovulated; at all later stages of lactation, six or seven days after being returned to the male > or = 50% of females came into oestrus, mated and ovulated. The vaginal smears of most females in isolation were typical of post oestrus on Day 2; after being returned to the male on Day 11, these females came into oestrus in seven days, mated and ovulated. The results show that suckling a young in the pouch does not suppress ovulation in this species provided that an adult male is present. Moreover, the results indicate that the mechanism of male-induced ovulation 24 h post partum differs from that of the remainder of the pouch suckling period.

Duration of embryonic diapause in the brush-tailed bettong, Bettongia penicillata (Potoroidae): effect of age of quiescent corpus luteum

1996 ◽  
Vol 8 (4) ◽  
pp. 807 ◽  
Author(s):  
MJ Smith
Keyword(s):  
Corpus Luteum ◽  
Post Partum ◽  
Embryonic Diapause ◽  
Maximum Duration ◽  
Bettongia Penicillata ◽  
Diapause Embryo ◽  
Effect Of Age

It has been shown that changes to the frequency of sucking by the pouch young do not affect the time of reactivation of the quiescent corpus luteum and diapause embryo in Bettongia penicillata; these observations led to the suggestion that the corpus luteum may have an inherent maximum duration of quiescence. The aim of the present study was to investigate the effect of the age of the corpus luteum on the timing of its reactivation. Ovulation fails to occur post partum in female B. penicillata isolated from males, and the introduction of a male B. penicillata induces oestrus in females suckling a young in the pouch. Oestrus was induced from Day 23 of lactation to Day 76, in different females, and the corpus luteum became quiescent. All parturitions occurred between Day 95 and Day 103 of lactation (average, Day 98.8), at the time expected if the corpus luteum had been formed post partum. Duration of quiescence of the corpus luteum ranged from 60 days to 10 days, compared with 83.9 +/- 0.43 days in females that mated post partum. The results show that the age of the corpus luteum does not affect the timing of its redevelopment and release of the embryo from diapause near the end of the period of the young being suckled within the pouch.

Control of pregnancy, parturition and luteolysis in marsupials

1990 ◽  
Vol 2 (5) ◽  
pp. 535 ◽  
Author(s):  
LA Hinds
Keyword(s):  
Life Span ◽  
Corpus Luteum ◽  
Post Partum ◽  
Secretory Activity ◽  
Extrinsic Factors ◽  
Pituitary Prolactin

In most eutherian species the function of the corpus luteum (CL) is influenced by extrinsic factors and it is subordinate to the pituitary, placenta, or uterus. In contrast, in marsupials the CL is relatively autonomous. Although the pituitary is essential for the formation of the CL, thereafter the secretory activity of the CL is independent of luteotrophic support, and the uterus is not luteolytic. Furthermore, the life span of the CL is unaffected by pregnancy, except in the Macropodidae (kangaroos and wallabies), in which the secretory activity of the CL is shortened under the influence of the fetus. At parturition the macropodid fetus, possibly via a release of glucocorticoids, causes the release of prostaglandins, presumed to be of uterine origin. The effect of the prostaglandin is to induce the release of prolactin from the maternal pituitary. Prolactin, and not prostaglandin, induces luteolysis and advances the events of post-partum oestrus. In the non-pregnant cycle, the mechanism of luteolysis is different; it does not involve prolactin, and the luteolytic signal is of non-uterine, possibly intrinsic, origin.

Oestrous cycle and gestation length in the musky rat-kangaroo, Hypsiprymnodon moschatus (Potoroidae : Marsupialia)

2001 ◽  
Vol 49 (1) ◽  
pp. 37 ◽  
Author(s):  
Shan Lloyd
Keyword(s):  
Epithelial Cells ◽  
Captive Breeding ◽  
Common Ancestor ◽  
Post Partum ◽  
Reproductive Physiology ◽  
Oestrous Cycle ◽  
Gestation Length ◽  
Vaginal Smears ◽  
Breeding Colony ◽  
Male And Female

Wild-caught male and female H. moschatus were maintained in a captive breeding colony. Vaginal smears were taken three times a week until oestrous cycles were detected and gestation lengths approximated. Thereafter, smears were usually taken daily when oestrus was expected. The gestation period (considered to be the number of days from the detection of sperm in the smear until the day young were found in the pouch) was found to last 19 days. Sperm were usually detected in the smear two days before the influx of semi-cornified and cornified epithelial cells, which occurred 17 days before parturition. A pre- or post-partum oestrus was not detected and females did not return to oestrus until at least 6 days after the removal of the last pouch young. H. moschatus has the shortest recorded gestation for any macropod, and gestation occupies approximately 75% of the oestrous cycle. The reproductive physiology of H. moschatus is similar to that of most phalangerids, which may be indicative of a common ancestor.

Reproduction of the Red-Bellied Pademelon Thylogale billardierii (Marsupialia)

1982 ◽  
Vol 9 (1) ◽  
pp. 27 ◽  
Author(s):  
RW Rose ◽  
DJ McCatney
Keyword(s):  
Corpus Luteum ◽  
Post Partum ◽  
Oestrous Cycle ◽  
Seasonal Breeder ◽  
The Mean ◽  
Duration Of Gestation

'Thylogale billardierii, which is abundant in Tasmania, is a seasonal breeder with most births in the months April, May and June. Parturition is followed by mating, and the zygote so produced remains dormant until either sucking becomes intermittent near the end of pouch life or the young is lost. The mean length of the oestrous cycle was determined at 30.3 days, not significantly longer than the duration of gestation (30.2 days). Removal of pouch young results in the birth of a new young 28.7 days later. Removal of the corpus luteum results in oestrus 11 days later. Pouch life is 202 days, and vacation of the pouch by the young coincides precisely with parturition and post-partum mating. The young mature at about 14-15 months.

Comparison of reproductive responses after PGF2α and GnRH-PGF2α oestrous synchronisation schemes in Holstein cows

2001 ◽  
Vol 26 (2) ◽  
pp. 467-470
Author(s):  
J.F. Cox ◽  
F. Saravia ◽  
O. Torrealba ◽  
A. Zavala ◽  
A. Lobos
Keyword(s):  
Dairy Cows ◽  
Corpus Luteum ◽  
Detection Efficiency ◽  
Post Partum ◽  
Conception Rate ◽  
Milk Samples ◽  
Reproductive Response ◽  
Holstein Friesian ◽  
Breeding Schemes ◽  
Friesian Cows

AbstractControlled breeding schemes for oestrous detection constitutes a proactive technical response that balances the infrastructural requirement for a profitable dairy operation and the demands for optimal animal performance. The present study compared (a) the reproductive response of a treatment based on a short vs longer-acting PGF2α analogue (tiaprost vs luprostiol), and (b) the reproductive response after a treatment of GnRH-PGF2α vs PGF2α alone for synchronizing dairy cows. Holstein-Friesian cows averaging 9000 kg milk/lactation and fed according to their requirements were used in the study. Cows were cyclic, at least 60 days post partum and were clinically sound before being considered for the experiments. In Experiment 1, animals were synchronised using an i.m. injection of either 15 mg of luprostiol or 0.75 mg of tiaprost, based on ultrasonic diagnosis of a corpus luteum. Animals were inseminated at observed oestrus. In Experiment 2, cows were synchronised, at random, by either an injection of 10pg ofbuserelin (day 0) followed by 0.75 mg of tiaprost at day 7 (GnRH-PGF2α) orjust 0.75 mg of tiaprost (PGF2α). For both treatments only cows with an ultrasonically detected corpus luteum were treated. Animals were inseminated at oestrus. At the time of treatment and again 3 days later, milk samples were collected and assayed for progesterone by RIA. Cows with progesterone concentrations >1 ng/ml were considered to have corpus luteum. Luteolysis was considered to have occurred when concentrations of progesterone were > 1 ng/ml at day 0 and <0.8 ng/ml at day 3. In Experiment 1, both analogues gave similar results in terms of induced luteolysis [luprostiol: 36/39 (92.3%) vs tiaprost: 36/41 (87.8%)], oestrous detection efficiency [luprostiol: 26/36 (72.2%) vs tiaprost: 30/36 (83.3%], oestrous distribution [day 2, 3 and 4, respectively: luprostiol: 26.9%, 50.0%, 19.2% vs tiaprost: 36.7%, 50.0%, 13.3%], and conception rates [luprostiol: 12/25 (48.0%) vs tiaprost: 14/28 (50.0%); P>0.05]. In Experiment 2, oestrous detection efficiency, interval to oestrus and conception rate were similar between treatments [97/149 (65.1%), 71.1 h, 43/95 (45.3%) for PGF2α vs 130/188 (69.1%), 68.2h, 65/126 (51.6%) for GnRH-PGF2α, respectively]. However the oestrous distribution was more concentrated in GnRH-PGF2α treated animals (P<0.01).

scholarly journals The development and morphology of the gonads of the mouse.— Part I. The morphogenesis of the indifferent gonad and of the ovary

1927 ◽  
Vol 101 (711) ◽  
pp. 391-409 ◽  
Keyword(s):  
Corpus Luteum ◽  
Sexual Maturity ◽  
Post Partum ◽  
Subsequent Paper ◽  
Adult Ovary

The work described in this series of papers was carried out with a view to furnishing controls of the experiments on the mouse undertaken in collaboration with Dr. A. S. Parkes and others. This paper deals with the development of the indifferent gonad of the mouse, up to the stage at which it differentiates into an ovary or a testis. This takes place on the 12th day post coitum , when the testis can first be distinguished. The ovaries remain in the indifferent stage for some time longer, but can be identified by a process of elimination. The present paper is concerned also with the development of the ovary from the time when sex can be distinguished until sexual maturity (8 weeks post partum ). It is not proposed to consider here the structure of the maturing follicle, the process of atresia, or the formation of the corpus luteum. These problems will be reserved for a subsequent paper on the adult ovary of the mouse.

A note on the induction of ovulation in lactating red deer hinds prior to the breeding season

1989 ◽  
Vol 49 (1) ◽  
pp. 134-138 ◽  
Author(s):  
M. W. Fisher ◽  
P. F. Fennessy ◽  
G. H. Davis
Keyword(s):  
Corpus Luteum ◽  
Breeding Season ◽  
Untreated Control ◽  
Red Deer ◽  
Osmotic Pump ◽  
Induction Of Ovulation ◽  
Induced Ovulation ◽  
Pre Treatment

Methods of inducing ovulation 3 weeks prior to the onset of the breeding season were evaluated in lactating adult red deer. Following 11 days of intravaginal progesterone pre treatment, hinds were either untreated (control), or given 300 i.u. PMSG i.m. or 500 mglh GnRH s.c. by osmotic pump. All hinds were laparoscoped 7 days after progesterone withdrawal to record the presence or absence of a corpus luteum on the ovaries, Laparoscopy showed 0113 control, 11113 PMSG and 8/13 GnRH-treated hinds ovulated indicating that during lactation, both methods of inducing ovulation are similarly effective, However, although these treatments induced ovulation, fertility as assessed from calving records, was poor.

scholarly journals Anatomical and histological changes during the oestrous cycle in the mare

1941 ◽  
Vol 130 (858) ◽  
pp. 1-23 ◽  
Keyword(s):  
Corpus Luteum ◽  
Reproductive Organs ◽  
Oestrous Cycle ◽  
Maximum Diameter ◽  
Histological Changes ◽  
Graafian Follicle ◽  
Heat Period ◽  
To Come ◽  
Time Required ◽  
Dominant Part

The mares chosen for the investigation of the changes in the reproductive organs during the oestrous cycle were kept under observation for some time before they were killed. The duration of the heat period in these animals was 7 days and the length of the dioestrus was 16 days. Ovulation takes place at about a day before the end of oestrus. The size of the ovary during the oestrous cycle is chiefly influenced by the growing Graafian follicle. The number of follicles present at different stages varies greatly. The numerous small follicles present at the beginning of oestrus disappear later in the cycle; it is suggested that this may be due to the lack of follicle-stimulating hormone. The colour of the corpus luteum varies greatly at different stages of the cycle. The rupture of the follicle is associated with some bleeding. The active stage of the corpus luteum is very short, and the maximum diameter of the corpus luteum seems to be always below that of the Graafian follicle. The greater development of the Graafian follicle, with its secretion of oestrin, in the mare leads to its playing a more important role than in the cow and the sow, in which species the corpus luteum takes a m ore dominant part in the cycle. It appears that the much longer oestrus in the mare than in the cow is due to the longer time required by the follicle to come to the surface and to break through. This is probably due to the peculiar structure of the ovary in the mare, since the ovulation, which is spontaneous, can only occur in the small ovulation fossa. No pronounced secretion stage occurs during oestrus in the Fallopian tubes.

Neonatal exposure to Δ9-tetrahydrocannabinol enhances sexual responses in the adult male mouse

1986 ◽  
Vol 110 (3) ◽  
pp. 517-523 ◽  
Author(s):  
P. Shrenker ◽  
R. Stegar ◽  
A. Bartke
Keyword(s):  
Adult Male ◽  
Post Partum ◽  
Serum Testosterone ◽  
Whole Body ◽  
Plasma Testosterone ◽  
Treatment Groups ◽  
Sexual Responses ◽  
Adult Plasma ◽  
Lh Releasing Hormone ◽  
Oral Doses

ABSTRACT From day 1 post partum to postnatal day 5, lactating female mice were given daily oral doses of 25 μl sesame oil, 0·5 mg tetrahydro-6,6,9-trimethyl-3-pentyl-6H-dibenzo(b,d)pyran-1-ol (Δ9-tetrahydrocannabinol; THC)/kg or 50 mg THC/kg in 25 μl oil. Additionally, the pups were given 20 μl oil, 10 μg testosterone or 20 μg testosterone in 20 μl oil s.c. from days 1 to 5 of age. This regimen resulted in nine treatment groups. At 60 days of age, all males were castrated and their testes weighed. After castration, each mouse was implanted s.c. with a 5 mm length of testosterone-filled silicone elastomer capsule. When adult they were tested for male copulatory behaviour. Following behavioural testing the animals were bled by cardiac puncture for measurement of plasma testosterone levels, and their hypothalami removed and assayed for dopamine, noradrenaline, 5-hydroxytryptamine (5-HT) and LH-releasing hormone (LHRH). In addition, another two groups of pregnant females were given daily oral doses of 0·5 or 50 mg THC/kg or oil during the first 3 or 5 days of lactation. The male pups were either decapitated for collection of trunk blood or homogenized for determination of serum or whole body testosterone concentrations. Neonatal administration of THC altered adult male sexual responses and had no effect on hypothalamic noradrenaline, 5-HT and LHRH concentrations. There were large increases in serum testosterone concentrations in neonates after maternal THC treatment, although these differences were not significant. Additionally, THC did not influence the testosterone content of neonatal tissue or the testosterone concentration of adult plasma. These results suggest strongly that the effect of THC on male sexual responses is not mediated by its effect on adult hypothalamic neurotransmitter concentrations. Some other potential mechanisms are discussed. J. Endocr. (1986) 110, 517–523

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