Prostaglandin in the peripheral plasma of tammar wallabies during parturition

1986 ◽  
Vol 111 (1) ◽  
pp. 103-109 ◽  
Author(s):  
P. R. Lewis ◽  
T. P. Fletcher ◽  
M. B. Renfree

ABSTRACT Tammar wallabies (Macropus eugenii) were observed for 7 days, 24 h/day, at the expected time of birth in two consecutive breeding seasons. Blood was collected from the lateral tail vein 1–2 days before birth, then at 10- to 20-min intervals in the peripartum period and less frequently to 30-h post partum. Plasma was assayed for the prostaglandin metabolite 13, 14-dihydro-15-oxo-prostaglandin F2α (PGFM), progesterone and LH. An assay for PGFM was validated which allows direct measurement in 100 μl unextracted plasma with a sensitivity of 0·14 nmol/l (50 pg/ml). There was a short-lived peak of PGFM immediately before or at birth (7·15 ± 2·52 nmol/l; 2536± 892 pg/ml) which declined to less than 0·28 nmol/l (100 pg/ml) within 2-h post partum. Progesterone concentrations declined about the time of birth, coincident with the peak of PGFM, and reached levels observed in lactationally quiescent animals by 16-h post partum, which was also the time of the LH peak. The transient prostaglandin pulse was detected only by frequent sampling and suggests that, as in other mammals, prostaglandin is important in parturition. J. Endocr. (1986) 111, 103–109

1990 ◽  
Vol 2 (1) ◽  
pp. 79 ◽  
Author(s):  
TP Fletcher ◽  
G Shaw ◽  
MB Renfree

Female tammar wallabies were treated with the dopamine agonist bromocriptine at the end of pregnancy to suppress the peripartum pulse of plasma prolactin. The animals were subsequently observed, and a series of blood samples taken to define the hormonal profiles before and immediately after parturition. Birth was observed in 4/5 control animals and occurred in 8/9 bromocriptine-treated animals. The peripartum peak in plasma PGFM concentrations was not affected by bromocriptine although the pulse of prolactin normally seen at parturition was completely abolished. The timing of luteolysis was apparently unaffected, as plasma progesterone concentrations fell similarly in both treated and control animals immediately after parturition. However, all of the neonates of the bromocriptine-treated animals died within 24 h, possibly because of a failure to establish lactation. Subsequent onset of post-partum oestrus was delayed or absent both in control and in bromocriptine-treated animals, suggesting that the frequent blood sampling and disturbances in the peripartum period interfered with these endocrine processes. It is concluded that both prolactin and prostaglandin can induce luteolysis in the pregnant wallaby, but that the normal sequence of events results from a signal of fetal origin inducing a prostaglandin release from the uterus, which in turn releases a pulse of prolactin that induces a progesterone decline.


1983 ◽  
Vol 96 (1) ◽  
pp. 155-161 ◽  
Author(s):  
C. H. Tyndale-Biscoe ◽  
L. A. Hinds ◽  
C. A. Horn ◽  
G. Jenkin

Concentrations of progesterone, prolactin, LH and 13,14 dihydro-15-keto-prostaglandin F2α (PGFM) were measured in plasma of eight tammar wallabies at 8-hourly intervals during the end of pregnancy and post-partum oestrus initiated by removing the pouch young, and during the end of the oestrous cycle, similarly initiated. In the non-pregnant cycle oestrus occurred 29·7 ± 0·7 (mean ±s.e.m.) days after initiation of the cycle, was preceded by a slow decline in progesterone concentration from 1·6 nmol/l to less than 0·64nmol/l and was followed by a preovulatory peak of LH 5·3± 3·9 h later. In the pregnant cycle birth occurred 26·1±0·2 days after removing the pouch young and was followed 8·0 ± 2·1 h later by oestrus and 16·0± 2·5 h by an LH peak. The latter events thus occurred 3·2 days earlier in the pregnant than in the non-pregnant cycle. Parturition coincided with a very rapid decline in progesterone and a transient high peak of prolactin. In two females sampled less than 25 min after parturition there was a transient peak of PGFM but in all others the concentrations of PGFM remained basal throughout. It is suggested that the fetus and/or placenta is involved in both the premature decline in progesterone and the initiation of parturition and that onset of oestrus and ovulation, being a consequence of a decline in progesterone, are therefore also determined by the fetus.


Reproduction ◽  
2000 ◽  
pp. 49-57 ◽  
Author(s):  
SD Johnston ◽  
MR McGowan ◽  
P O'Callaghan ◽  
R Cox ◽  
V Nicolson

As an integral part of the development of an artificial insemination programme in the captive koala, female reproductive physiology and behaviour were studied. The oestrous cycle in non-mated and mated koalas was characterized by means of behavioural oestrus, morphology of external genitalia and changes in the peripheral plasma concentrations of oestradiol and progestogen. The mean (+/- SEM) duration of the non-mated oestrous cycle and duration of oestrus in 12 koalas was 32.9 +/- 1.1 (n = 22) and 10.3 +/- 0.9 (n = 24) days, respectively. Although the commencement of oestrous behaviour was associated with increasing or high concentrations of oestradiol, there were no consistent changes in the morphology or appearance of the clitoris, pericloacal region, pouch or mammary teats that could be used to characterize the non-mated cycle. As progestogen concentrations remained at basal values throughout the interoestrous period, non-mated cycles were considered non-luteal and presumed anovulatory. After mating of the 12 koalas, six females gave birth with a mean (+/- SEM) gestation of 34.8 +/- 0.3 days, whereas the remaining six non-parturient females returned to oestrus 49.5 +/- 1. 0 days later. After mating, oestrous behaviour ceased and the progestogen profile showed a significant increase in both pregnant and non-parturient females, indicating that a luteal phase had been induced by the physical act of mating. Progestogen concentrations throughout the luteal phase of the pregnant females were significantly higher than those of non-parturient females. Parturition was associated with a decreasing concentration of progestogen, which was increased above that of basal concentrations until 7 days post partum.


1993 ◽  
Vol 136 (1) ◽  
pp. 17-NP ◽  
Author(s):  
J. M. Wallace ◽  
M. G. Thompson ◽  
R. P. Aitken ◽  
M. A. Cheyne

ABSTRACT Induction of ovulation early post partum in sheep is associated with a high incidence (30–40%) of premature luteolysis. The present study was designed to characterize oxytocin receptor levels, oxytocin-stimulated inositol phosphate (IP) turnover (second messenger) and oxytocin-stimulated prostaglandin F2α (PGF2α) release in the endometrium of post-partum ewes induced to ovulate 21 days after parturition and expected to exhibit a range of corpus luteal functions subsequently. Ovulation was induced on day 21 post partum using a controlled internal drug release device and pregnant mare serum gonadotrophin, and uterine tissues were collected on days 5, 10 or 15 of the cycle (n = 4/day). A further 12 ewes whose interval from previous parturition exceeded 150 days were similarly treated and acted as controls. Measurement of daily peripheral progesterone concentrations revealed that while all control ewes exhibited normal luteal function, abnormal luteal function was evident in two, two and one post-partum ewes studied on days 5, 10 and 15 of the cycle respectively. Oxytocin receptor binding was detected (by receptor-binding assay and in-vitro autoradiography) in the endometrium and myometrium of post-partum ewes at all three stages of the oestrous cycle but only at day 15 in control ewes. To determine IP turnover, 100 mg caruncular endometrium was incubated in duplicate for 2·5 h with 10 μCi [3H]inositol and treated with 0 or 2 μmol oxytocin/l for 30 min, then [3H]inositol mono-, bis- and trisphosphates were quantified. Oxytocin stimulated total IPs in all day-5 and day-15 post-partum ewes, in three of four day-10 ewes and in all day-15 control ewes. Basal endometrial PGF2α release measured in triplicate (100 mg/well) during a 2 h incubation was higher in post-partum versus control ewes on days 5 and 10 but not on day 15 of the cycle. Similarly, oxytocin stimulated PGF2α release to varying levels at all stages of the cycle in post-partum ewes but only on day 15 in control ewes. Irrespective of the treatment group endometrial oxytocin receptor number was significantly (P < 0·001) correlated with oxytocin-stimulated IP turnover and PGF2α release. Thus the induction of ovulation and the subsequent luteal phase in post-partum ewes is against a back ground of high oxytocin receptor expression and enhanced PGF2α release which in some ewes may contribute to abnormal luteal function. Journal of Endocrinology (1993) 136, 17–25


Reproduction ◽  
2011 ◽  
Vol 141 (3) ◽  
pp. 333-342 ◽  
Author(s):  
Fernando A Rivera ◽  
Luís G D Mendonça ◽  
Gláucio Lopes ◽  
José E P Santos ◽  
Rolando V Perez ◽  
...  

Fertility of lactating dairy cows is associated with reduced progesterone (P4) concentration compared with nonlactating animals. The objective of the current study was to determine whether P4 during growth of the first follicular wave (FFW) affects embryo quality. Lactating Holstein cows at 33±3 days post partum were allocated to one of three treatments. Cows in the FFW and FFW with P4 (FFWP) treatments started the superstimulation protocol on day 1 of the estrous cycle and second follicular wave (SFW) cows started the superstimulation protocol on estrous cycle day 7. Cows were superstimulated with 400 mg of NIH-FSH-P1 (FSH) given twice daily for 5 days, two prostaglandin F2α (PGF2α) injections given with the ninth and tenth injections of FSH, GNRH given 48 h after the first PGF2α injection, and timed insemination 12 and 24 h after the GNRH injection. Cows in the FFWP treatment received two intravaginal P4 inserts during the superstimulation. Embryos were recovered 6.5 days after artificial insemination and excellent/good and fair embryos were frozen and transferred. Blood was sampled daily from estrous cycle day 0 until insemination from donor cows. During the superstimulation protocol, P4 was (P<0.01) greatest for SFW cows followed by FFWP and FFW cows respectively. The percentage of embryos–oocytes from SFW and FFWP cows classified as excellent/good and fair embryos was (P=0.02) greater than those of FFW cows. Pregnancy per embryo transfer was not (P≥0.73) affected by embryo donor treatment. Reduced embryo quality of cows induced to ovulate the follicles from the first follicular wave is a consequence of reduced P4 during follicle growth.


1974 ◽  
Vol 63 (1) ◽  
pp. 125-135 ◽  
Author(s):  
RICHARD BARANCZUK ◽  
G. S. GREENWALD

SUMMARY Oestrone (OE1), oestradiol (OE2) and progesterone were measured by radioimmunoassay in the same samples of peripheral plasma from pregnant and lactating hamsters. The levels of progesterone during most of pregnancy did not exceed the values found during the first 2 days of the oestrous cycle. However, on day 14 of pregnancy (2 days before parturition) the level of progesterone abruptly increased to 29 ng/ml and fell rapidly thereafter. Hysterectomy on day 12 of pregnancy resulted in baseline levels of progesterone ( < 2 ng/ml) on day 13 and no peak in progesterone comparable to the one observed on day 14 of normal gestation. Injecting progesterone on day 14 or later prolonged gestation and caused maternal and foetal death. Oestradiol concentration showed peaks on days 7 (67·3 pg/ml), 11 (117·6 pg/ml) and 14 (81·8 pg/ml) of pregnancy and dropped precipitously between days 14 and 16 of pregnancy. The highest values obtained on day 11 correlated with the maximal proliferation of antral follicles. The abrupt decline of oestrogen concentration at parturition is different from the pattern found in the mouse and rat but is consistent with the lack of post-partum ovulation in the hamster. Injecting 50–150 μg oestradiol cyclopentylpropionate between days 12 and 16 did not interfere with parturition by the morning of day 16. Oestrone was detectable throughout pregnancy; the levels were lower than for OE2. In general, the oestrogen patterns were parallel. During lactation, progesterone secretion remained relatively constant at about 10–11 ng/ml, presumably synthesized by the hypertrophied interstitium which is the dominant ovarian tissue. In most instances OE1 and OE2 were not detectable during lactation, consistent with the absence of antral follicles.


1993 ◽  
Vol 56 (2) ◽  
pp. 207-210 ◽  
Author(s):  
N. F. G. Beck ◽  
B. Davies ◽  
S. P. Williams

AbstractAn experiment was designed to determine whether combining a single injection of 125 μg prostaglandin F2α analogue (PGF) with a 5-day progestagen pessary treatment (PPT) would obviate the problem with refractory animals that occurs when randomly cycling ewes are synchronized with PGF alone. The efficacy of the combined treatment, in comparison with single and double dose PGF regimes, was also assessed.A total of 210 ewes were used in this investigation conducted during the 1989 and 1990 breeding seasons. In both breeding seasons, 100% of the ewes treated with PGF combined with PPT were mated by fertile rams within a 3-day period, compared with 52·9% of ewes treated with a single injection PGF or 100% of ewes treated with two injections of PGF, 11-days apart. Returns to service for the three groups were 14·2%, 16·2% and 17·4%, respectively. There was no effect of treatment on lambing performance in 1989. However, in 1990 there were differences between groups in gestation length and birth weight, but these were attributable to enzootic abortion. The results demonstrate that PGF combined with PPT will produce levels of oestrous synchronization and fertility comparable with other methods.


1997 ◽  
Vol 9 (2) ◽  
pp. 243 ◽  
Author(s):  
K. Basden ◽  
D. W. Cooper ◽  
E. M. Deane

A study has been made of the development of four lymphoid tissues from birth to maturity in the tammar wallaby Macropus eugenii —the cervical and thoracic thymus, lymph nodes and gut-associated lymphoid tissue (GALT). The development of these tissues in the tammar wallaby is similar to that in two other marsupials, the quokka Setonix brachyurus and the Virginian opossum Didelphis virginiana. Lymphocytes were first detected in the cervical thymus of the tammar at Day 2 post partum and in the thoracic thymus at Day 6. They were subsequently detected in lymph nodes at Day 4 and in the spleen by Day 12 but were not apparent in the GALT until around Day 90 post partum. By Day 21, the cervical thymus had developed distinct areas of cortex and medulla and Hassall’s corpuscles were apparent. The maturation of other tissues followed with Hassall’s corpuscles in the thoracic thymus by Day 30 and nodules and germinal centres in the lymph nodes by Day 90. Measurement of immunoglobulin G concentrations in the serum of young animals indicated a rise in titre around Day 90 post partum, correlating with the apparent maturation of the lymphoid tissues.


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