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Concentrations of serum oxytocin, cortisol, progesterone and estradiol in pregnant rats were assayed by radioimmunoassay methods. The levels of these hormones increased in pregnancy. Around the parturition, oxytocin or estradiol did not show any change, cortisol increased, and progesterone decreased prominently. The trigger of initiation of labor was discussed.
Prostaglandin F2alpha (PGF2alpha) was infused intra-aortically at different rates into rats for 11-5 h from day 18 of gestation. At doses in excess of 5 mug/h premature delivery invariably occ'rred 40-41 h later. At lower doses an all-or-none effect was observed, some animals delivering prematurely and others continuing to term. Parturition could not be induced earlier than 40 h after the start of the treatment even by a continuous infusion of PGF2alpha, suggesting that the luteolytic role of PGF2alpha is more important than its oxytocic action in this case. The rate of fall in plasma progesterone was greater in the rats delivering prematurely than those delivering at term, although the final concentrations of between 15 and 30 ng/ml at delivery were the same. Labour appeared more normal in the animals receiving PGF2alpha than in those which had been bilaterally ovariectomized. The possible significance of this in relation to an effect of PGF2alpha on oestrogen secretion is discussed.
Using specific radioimmunoassays, 17alpha,20alpha-dihydroxypregn-4-en-3-one and progesterone were measured in maternal utero-ovarian venous plasma from four sheep during parturition induced with dexamethasone and two sheep at spontaneous delivery. 17alpha,20alpha-Dihydroxypregn-4-en-3-one was also measured in maternal jugular venous and foetal posterior vena caval plasma from one dexamethasone-induced animal over the same period. Basal utero-ovarian venous levels of 17alpha,20alpha-dihydroxypregn-4-en-3-one were in the range 3-7 ng/ml; at the time of the pre-labour fall in maternal progesterone, the concentration of 17alpha-20alpha-dihydroxypregn-4-en-3-one increased, reaching 17-76 ng/ml at delivery. Maternal levels fell rapidly after delivery. In contrast to foetal progesterone concentrations, which are low, foetal 17alpha,20alpha-dihydroxypregn-4-en-3-one levels were approximately the same as those in the maternal utero-ovarian vein. Maternal jugular venous levels in one animal were 50-80% of those in the utero-ovarian vein. These findings confirm earlier results obtained in vitro which indicated that exposure to glucocorticoid results in increased activity of a steroid 17alpha-hydroxylase in the ovine foetal placenta.
Levels of prolactin and LH were determined in serum and pituitary during the last days of pregnancy and post partum in rats bearing single and multiple embryos. In rats with a single embryo serum prolactin and LH levels were significantly lower during the last 2 days of pregnancy and post partum than in rats bearing multiple embryos. While large increases were recorded in serum prolactin and LH levels in the rats with multiple embryos between days 21 and 22 of gestation, in the group with single embryos changes occurred in LH level only. Throughout the experiment pituitary prolactin was lower in rats with a single embryo than in those with multiple embryos in spite of the sharp drop in prolactin level in the group with multiple embryos from day 21 to 22. No differences were observed in the pituitary LH levels of either group during the days preceding parturition, but in the rats with multiple embryos there was a sharp drop in LH level post partum. It seems that the reduced serum prolactin level in the rats with a single embryo was associated with inhibition of pituitary prolactin synthesis and release, whereas the decreased serum LH level resulted from impaired release but not synthesis. These results support the hypothesis of a regulatory role for the placenta in pituitary prolactin and LH synthesis and release, either by hypothalamus-pituitary stimulation, or perhaps by way of the ovaries, through regulation of ovarian steroid production.
The concentrations of 13, 14-dihydro-15-oxo-prostaglandin F(PGFM), the stable metabolite of prostaglandin F, were measured in the plasma of catheterized mares and foetuses and non-catheterized thoroughbred mares and ponies during the last months of gestation. The plasma concentration of PGFM increased gradually towards term in all groups of animals. During the operation for insertion of catheters, maternal and foetal concentrations of PGFM were high, but the values fell to basal levels 24--48 h after the operation. It was found the preoperative starvation (24 h) led to a rise in the concentration of PGFM in the maternal plasma. The raised concentrations of PGFM during the operation were associated with low progestogen and high oestrogen concentrations in umbilical venous plasma. The subsequent survival period of the catheterized foal was inversely related to the maximum concentration of PGFM were studied during normal parturition in thoroughbred mares, during oxytocin-induced delivery in non-catheterized ponies and during premature delivery or abortion in the catheterized animals. The greatest increase in the concentration of PGFM was seen in the thoroughbred animals during second-stage labour; oxytocin also resulted in a very rapid rise in the level of PGFM, which remained high until delivery. In the catheterized animals, the birth of live foetuses was associated with a rise in the concentration of PGFM in both foetal and maternal plasma during the last 2 h before delivery. Less consistent changes were found during abortion.
The concentration of thromboxane B2 has been measured in the plasma of women during late pregnancy, during term and pre-term labour, in women with pre-eclampsia and in umbilical cord arterial and venous plasma. In addition, the rates of production of thromboxane B2 in vitro were determined for placental tissues obtained after spontaneous vaginal delivery or elective Caesarean section. The results obtained indicate significant differences during parturition between the sources and controlling mechanisms of thromboxane and prostaglandin production.
Plasma oxytocin concentrations were measured during late pregnancy, parturition and lactation in the miniature pig. Measurements were made of plasma oestradiol, oestrone and progesterone to determine whether there was any relationship between the concentrations of oxytocin and these steroids in the circulation. Plasma oxytocin concentrations were low or undetectable in late pregnancy. Rises of up to 68.8 mum./ml were seen at the time of delivery of the foetuses and at the expulsion of the placenta. The only steroid that seemed to relat to oxytocin release was progesterone. Oxytocin release was consistently seen when progesterone concentrations had fallen to below 10 ng/ml but no increase in concentration was observed while oestrone and oestradiol increased to their maximum concentrations of 3.86--11.6 and 0.43--0.70 ng/ml respectively. During lactation, when both oestrogen and progesterone concentrations were low, suckling caused the levels of oxytocin to increase to 7.4 muu./ml. These increases were greater during the first 2 weeks of lactation than later.
Epitestosterone, a product of the metabolism of androstenedione by the caprine placenta in vitro, is present in the plasma of the pregnant goat. The maternal concentrations of both epitestosterone and unconjugated oestrogens (mostly oestradiol-17 alpha) in the blood increased before parturition and dropped post partum. Measurement of arteriovenous differences at term indicated that epitestosterone was secreted by the uterus; its production was not dependent on the presence of corpora lutea. It is suggested that the concentration of epitestosterone (+ androstenedione + oestrogens) in maternal plasma may be used as an indicator of placental C-17,20 lyase activity; the slight rise in the concentration of these compounds prepartum suggests a relatively small increase in flow through this enzyme.
Cortisol:cortisone interconversion was studied in human decidua obtained from three groups of patients at term (37-42 weeks): before the onset of labour (at elective Caesarean section), after labour of spontaneous onset, and after labour of induced onset. When intact tissue was incubated with [3H]cortisol or [3H]cortisone in phosphate buffer without added substrate or cofactors, cortisone to cortisol was the dominant conversion. However, when damaged cells or tissue homogenates were used in the same conditions, the dominant direction of the reaction was reversed, with a large increase in oxidative (cortisol to cortisone) activity. Cortisol:cortisone interconversion was similar in the three groups of samples using either intact tissue or homogenates, as was the total 11 beta-hydroxysteroid dehydrogenase (11 beta-HSD) activity measured in tissue homogenates in the presence of added substrate (cortisol or cortisone) and cofactors (NADP+ or NADPH). Endogenous cortisol concentrations in decidua were higher than those of cortisone, and the ratio of cortisol to cortisone was similar in the three groups. These findings suggest that there are no changes in human decidual 11 beta-HSD activity in relation to parturition. Specific activity of 11 beta-HSD decreased at high protein concentrations, suggesting the presence of some enzyme inhibitor(s) in homogenized decidual tissue.
A controlled-delivery module based on microporous Accurel polypropylene tubing, implanted subcutaneously in the rat, was used to release oxytocin for at least 40 days both in vitro and in vivo. Using a dosage rate of approximately 650 ng oxytocin per day and implanting the device in rats on day 17 of pregnancy, the known physiological action of oxytocin in advancing labour was confirmed. The increased concentrations of oxytocin in the mothers gave rise to adverse effects; the course of labour was protracted during expulsions of the first pups and the birth weight was reduced. Postnatally, body development of the pups was also affected, although there was partial recovery when the pups started to feed independently. Both pre- and postnatal exposure of pups to an oxytocin-treated mother reduced their body water turnover measured at 1 month of age. The effects on the course of parturition and during lactation might be explained by a blockade of uterine and mammary gland oxytocin receptors respectively, thereby inhibiting a proper response to pulsatile endogenous oxytocin secretion. The changes in water metabolism, which are opposite to those described for the heterologous hormone vasopressin, are less easy to explain since maternal oxytocin is not supposed to pass the placenta. The results may indicate that clinical use of oxytocin for induction of labour and lactation may have hitherto unrecognized side-effects.
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 F2 alpha (PGFM), progesterone and LH. An assay for PGFM was validated which allows direct measurement in 100 microliter 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.
The aim of this study was to determine whether expression of prostanoid receptor genes varied with gestational age or labour in the decidua and chorion of baboons. Tissues were obtained at the time of Caesarean hysterectomy in 15 baboons, 10 prior to the onset of labour in the last third of pregnancy and 5 in spontaneous labour at term. Expression of prostanoid receptor genes was determined using Northern blot analysis and the level of expression was related to each of three housekeeping genes. Expression of the genes encoding the EP(1) and FP receptor in decidua and the EP(4) receptor in chorion was lower with advancing gestational age. Expression of the EP(2) receptor gene was lower in labour in decidua, whereas expression of the IP receptor gene was higher in labour in both decidua (twofold) and chorion (fourfold). It is concluded that there is a complex pattern of change in expression of prostanoid receptor genes in chorion and decidua with advancing gestational age and in association with labour. It seems likely that direct effects of prostaglandins on the choriodecidua may have an important role in parturition in the primate.
Thirteen multiparous (M; 451 kg, 6.1 body condition score) and 11 primiparous (P) Brahman cows (408 kg, 6.3 body condition score) were assigned randomly within parity to receive either 2-min uterine manipulation (UM) per rectum 35 d after calving or no UM (C). This resulted in four groups: MUM (n = 8), MC (n = 5), PUM (n = 5) and PC (n = 6). All animals received a jugular cannula on d 34. Blood samples were collected at 10-min intervals from 30 min prior to UM until 120 min after UM and at 20-min intervals through 300 min after UM. Plasma was harvested immediately and stored at -20 degrees C until RIA for 13, 14-dihydro-15 keto prostaglandin F2 alpha (PGFM). Number of PGFM peaks in 330 min and amplitude of these peaks were similar (P greater than .10) in MC (2.0 peaks, 445.6 pg/ml) and PC (1.8 peaks, 446.9 pg/ml). Response to UM differed (P less than .02) by parity. The PGFM response of UM and C primiparous cows did not differ. Mean PGFM concentrations between 70 and 300 min after UM were greater (P less than .05) in MUM than in MC cows. Area of the PGFM curve did not differ (P greater than .10) in primiparous groups but was greater (P less than .01) in MUM than in MC cows. Uterine manipulation 35 d after parturition increased plasma PGFM in M but not in P cows.
Primiparous rabbit does were mated within 12 h after parturition (d 0). They were immediately weaned (Group W; n = 31) or allowed to suckle 10 young rabbits (Group L; n = 32). Blood samples were collected at d 0, 7, 17, and 28. Feed intake and live weight were measured weekly and pregnant does (Group W, n = 24; Group L = 25) were slaughtered at d 28. Feed intake was 78% higher in L than in W females throughout gestation (P < .001). However, L females lost weight during the second half of gestation (-243 +/- 25 g) compared with W females, which gained weight (246 +/- 20 g). The weights of carcass, skin, and adipose tissues were severely reduced at d 28 in the L group (P < .01). Ovulation rate (11.0 +/- .3 corpora lutea) and early embryonic mortality (< d 15) were similar in both groups (12.3 +/- 2%), whereas late embryonic mortality (> or = d 15) was higher in L than in W does (13.9 +/- 3 vs 3.9 +/- 1%; P < .01). Fetal weight was reduced by nearly 20% in L compared with W females (P < .01). Plasma concentrations of progesterone were lower in L than in W females at d 7 and 17 (P < .001), whereas concentrations of estradiol were similar in both groups throughout gestation. These results indicate that fetal survival and development can be impaired in lactating females.
Cows that consume needles from Pinus ponderosa (PN) abort, but little is known about variables that affect consumption or response. These experiments were conducted to test the effects of several variables on pine needle-induced abortion. Cows were placed on experiment at 250 d of pregnancy and were either given ad libitum (AL) access to PN separate from other feed sources or the PN were ground and fed (2 kg.cow-1.d-1) mixed with the diet. In Exp. 1, cows were assigned to a 2 x 2 factorial experiment with adequate (AP) vs high-protein (HP) diets and no straw vs AL straw (S). All cows ate PN and aborted, and there were no effects (P > .5) on interval to parturition (IP). Consumption of PN (kg/d) was increased by HP (P < .1). In Exp. 2, cows were assigned to five treatments to test the effects on response to PN of magnesium supplementation, weathering the PN, and using silage rather than hay as the basal diet. Consumption of PN shortened IP (P < .01), but magnesium, weathering PN, and silage-based diets did not decrease the response to PN (P > .5). In Exp. 3, cows were assigned to five treatments to test the effects of aging needles after they were ground, feeding bentonite, and feeding a complete mineral supplement. Pine needles decreased IP (P < .01), and the effects of PN were greater when PN were aged or bentonite or minerals were added (all P < .05).(ABSTRACT TRUNCATED AT 250 WORDS)
The study involved 44 primiparous, 2-yr-old heifers and 74 multiparous cows, 3 or 4 yr old, bred to a single Charolais bull. Variables were dam age (heifer, H; or cow, C), restricted (RE) or forced (FE) exercise for the last 90 d precalving, and natural (NP) or induced (IP) parturition. The RE dams were held in drylots; FE dams were on range until d 260 to 267 and walked 3.2 km/d for feed and water. Dams with IP received 10 mg of flumethazone on d 269 of gestation. Diets for FE and RE dams contained the same hay and grain, but FE dams were fed in amounts projected to give weight changes approximating those of RE dams. All dams were calved in drylots; thereafter, all pairs were maintained together on pasture to the end of the study. Exercise did not affect dystocia score or incidence, increased feed requirement 31% (P < .01), and gave a 14.8% higher (P < .05) pregnancy rate in the subsequent 45-d breeding season. We hypothesize the increased pregnancy may have resulted from a feed-endocrine effect related to body weight gain, body composition-metabolic changes, or subsequent higher feed intake.(ABSTRACT TRUNCATED AT 250 WORDS)
Spring-calving Brahman cows (S) artificially inseminated to Brahman, Angus, or Tuli sires and fall-calving Brahman cows (F) naturally bred to Brahman were allotted randomly to receive 3.74% (LF; n = 9 S and 6 F), 5.20% (MF; n = 8 S and 6 F), or 6.55% dietary fat (HF; n = 8 S). Diets were formulated to contain differing fatty acid concentrations and to be isocaloric and isonitrogenous. Cows were bled and fed twice daily from 2 wk before expected calving date through d 21 after calving. Ultrasonography was performed on d 14 and 21 after calving. From d 21 to 90 after calving a sterile bull equipped with a chin-ball marker was placed with the cows to aid in estrus detection. In both seasons progesterone decreased (P < .01) and estradiol-17 beta increased (P < .01) as parturition approached. Cows receiving MF and HF had increased (P < .01) total numbers of follicles compared to LF cows, and cows receiving MF had larger (P < .01) follicles. During the spring, cows receiving HF and cows bred to Brahman or Tuli sires had longer (P < .01) gestation lengths. Progesterone concentrations before calving were affected (P < .01) by treatment x sire and estradiol-17 beta by a time x treatment interaction (P < .01). Cholesterol after calving was higher (P < .01) in HF cows than in LF or MF cows. In the fall, LF cows had heavier (P < .01) calves than cows receiving MF. Birth weight was also affected (P < .01) by treatment x sex of calf. Progesterone was affected (P < .01) by treatment x sex of calf. Estradiol-17 beta was affected (P < .01) by sex of calf and treatment x sex of calf. Across seasons, by d 90 after calving, 9 of 15 (60%) LF and 11 of 15 (73.3%) MF cows showed estrual behavior. Cows in the spring had increased (P < .01) numbers and larger follicles compared to the fall. In conclusion, dietary fat may influence steroid hormone concentrations before calving, calf birth weight and postpartum follicular populations; furthermore, follicular populations may also be influenced by season.
The effect of bull exposure on the resumption of estrous activity following parturition was studied in an experiment using mature Hereford and Hereford X Angus beef cows. In the spring of 1981 and 1982, cows were assigned by breed and calving date to one of two treatment groups. Cows were exposed to bulls either from 3 to 85 d postpartum (BE; n = 45, 1981; n = 35, 1982) or from 53 to 85 d postpartum (NE; n = 39, 1981, n = 36, 1982). Blood samples were collected from all cows once weekly from calving until 85 d postpartum to determine progesterone concentrations. The first increase in progesterone, which indicated onset of estrous cycles occurred at 43 +/- 2 vs 63 +/- 2 d (P less than .01) in 1981 and at 39 +/- 2 vs 61 +/- 3 d (P less than .01) postpartum in 1982 in BE cows and NE cows, respectively. Early postpartum exposure of cows to bulls reduced the postpartum anestrous interval.