EFFECT OF INTRA-UTERINE FOREIGN BODIES AND OF PROSTAGLANDIN ADMINISTRATION ON PROGESTERONE SECRETION DURING THE OESTROUS CYCLE OF THE GUINEA-PIG

1976 ◽  
Vol 70 (1) ◽  
pp. 39-45 ◽  
Author(s):  
F. R. BLATCHLEY ◽  
B. T. DONOVAN

SUMMARY The response of the guinea-pig corpus luteum to the luteolytic influence of glass beads placed in the uterus, or to prostaglandin administration, was followed by assay of the progesterone content of blood samples collected daily. Following the introduction of glass beads into the uterus early in the cycle, the secretion of progesterone was curtailed. Treatment with prostaglandin F2α over days 4–6 or 6–8 of the cycle temporarily depressed progesterone release without shortening the life of the corpora lutea. When the drug was administered over days 8–10, 10–12 or 12–14 the depression in progesterone was not followed by any recovery. These observations indicate that the response of the corpora lutea to a luteolytic influence changes during the oestrous cycle.

1979 ◽  
Vol 82 (3) ◽  
pp. 425-428 ◽  
Author(s):  
J. WATSON ◽  
C. E. PATEK

Prostaglandin F2α (PGF2α) secreted by the reproductive tissues of the pig in vitro was measured and it was found that the levels secreted by the corpus luteum and endometrium of early pregnant sows were significantly lower than those secreted by tissues during the late stage of the oestrous cycle. They were, however, comparable to levels secreted by tissues from the mid-stage of the oestrous cycle. Embryos also secreted significant amounts of PGF2α. Secretion of progesterone and oestradiol by the corpora lutea of both cyclic and pregnant pigs fell within accepted limits but embryos were also found to secrete significant amounts of oestradiol. The results suggest that luteal maintenance in the early pregnant pig is unlikely to be directly due to reduced synthesis of PGF2α.


1971 ◽  
Vol 50 (4) ◽  
pp. 625-635 ◽  
Author(s):  
DOREEN V. ILLINGWORTH ◽  
J. S. PERRY

SUMMARY The effects of hypophysial stalk-section on the growth and function of the corpus luteum of the non-pregnant guinea-pig have been compared with the effects of hypophysectomy (as previously described) and with the effects of prolactin administered to hypophysectomized animals. Stalk-section soon after ovulation did not impair the growth of the corpora lutea nor their ability to secrete progesterone. Stalk-section before day 9 of the oestrous cycle prevented the normal regression of the corpora lutea; they continued to grow and 3 weeks after ovulation were as large as those of pregnant animals, or of non-pregnant hysterectomized guinea-pigs. The corpora lutea regressed irregularly during the following 2 weeks. When performed on, or later than day 9, stalk-section did not prevent luteal regression at the normal time. Administration of prolactin (10 i.u./day) to hypophysectomized guinea-pigs restored the growth-rate of the corpora lutea, which reached sizes comparable to those of the normal cycle, and those of stalk-sectioned animals, by 10 days after ovulation. Our results indicate that prolactin can have substantial luteotrophic activity in the guinea-pig.


1992 ◽  
Vol 132 (1) ◽  
pp. 115-122 ◽  
Author(s):  
J. E. Sánchez-Criado ◽  
J. Th. J. Uilenbroek ◽  
B. Karels

ABSTRACT Administration of the antiprogesterone RU486 (2 mg/day) for 14 days to rats with a 5-day reproductive cycle resulted in an increase in both ovarian and pituitary weight in contrast with rats with a 4-day oestrous cycle. Luteal progesterone production decreased earlier in 4-day than in 5-day cyclic rats. Treatment of 5-day cyclic rats with antiprogesterone from the day of metoestrus onwards resulted in the advancement of the preovulatory prolactin surge by 24 h. Progesterone production by the corpus luteum was, however, not affected, indicating that in 5-day cyclic rats the corpora lutea are still functionally active at the time of the preovulatory surge of prolactin. They become, therefore, stimulated both in size and progesterone production. In contrast, the corpora lutea in 4-day cyclic rats are functionally inactive at the time of the preovulatory surge of prolactin, and prolactin acts luteolytically. In conclusion, the advancement of the preovulatory surge of prolactin by 24 h accounts, at least in part, for the increase in ovarian weight in 5-day cyclic rats after treatment with antiprogesterone. The results of these experiments do not agree with a direct effect of the antiprogesterone RU486 on progesterone secretion by the corpus luteum. Journal of Endocrinology (1992) 132, 115–122


Reproduction ◽  
2003 ◽  
pp. 205-210 ◽  
Author(s):  
EM Paslay ◽  
U Salli ◽  
F Stormshak ◽  

The aim of this study was to determine whether endogenous progesterone regulates synthesis and secretion of luteal oxytocin. In Expt 1, mature ewes (n = 5 per group) were assigned randomly to control or mifepristone (RU486) treatment groups. Ewes were injected s.c. twice a day with vehicle or 10 mg RU486 on days 5-7 of the oestrous cycle (oestrus = day 0). On day 8, after an i.v. injection with prostaglandin F(2alpha) (250 microg cloprostenol), venous blood samples were collected at frequent intervals to determine plasma oxytocin concentrations. Plasma oxytocin concentrations of RU486-treated ewes were not significantly different from those of control ewes. In Expt 2, ewes were injected s.c. each day with vehicle or 175 mg RU486 on days 2-5 of the oestrous cycle followed by administration of prostaglandin F(2alpha) on day 6. Four of five RU486-treated ewes showed 'split-oestrus' (oestrous behaviour for 36 h and then again at 84-108 h after the onset of initial oestrus). There was no significant difference in mean plasma oxytocin or progesterone concentrations between treatment groups. The mean masses of mature corpora lutea from control and RU486-treated ewes on day 6 of the oestrous cycle did not differ significantly (394.8 +/- 28.8 versus 319.5 +/- 48.3 mg). RU486-treated ewes contained mature corpora lutea, new corpora lutea (two of four ewes) and preovulatory follicles (>or= 10 mm, two of four ewes). The average interoestrous interval for RU486-treated ewes was 9 days more than that for control animals (26.2 +/- 2.9 versus 17 +/- 0.5 days; P < 0.025).


1970 ◽  
Vol 47 (2) ◽  
pp. 225-230 ◽  
Author(s):  
K. P. BLAND ◽  
B. T. DONOVAN

SUMMARY Regression of the corpora lutea in the guinea-pig could be accelerated by treatment with 10 μg. oestradiol benzoate daily over days 3–11 of the oestrous cycle. A single injection of 10 μg. oestradiol benzoate on day 3 was also effective. The luteolytic effect of oestrogen was abolished by hysterectomy, indicating that the uterus is involved in the mediation of the response. Progesterone (5 mg. daily over days 3–11) enhanced the luteal regression brought about by the presence of two glass beads in one horn of the uterus, but did not affect luteal size in otherwise intact females. Treatment of guinea-pigs with 5 mg. progesterone daily over days 2–5 or 4–7 failed to alter the length of the oestrous cycle.


1966 ◽  
Vol 52 (1) ◽  
pp. 72-90 ◽  
Author(s):  
R. Denamur ◽  
J. Martinet ◽  
R. V. Short

ABSTRACT The purpose of these experiments was to investigate the part played by the pituitary gland and the uterus in the control of the corpus luteum in the sheep. Six experiments were carried out, as follows: Hypophysectomy early and late in the oestrous cycle. Hypophysectomy on days 2–5 allowed the corpus luteum to continue secreting normal amounts of progesterone for up to 9 days, but thereafter the secretion declined. Hypophysectomy on days 9–10 caused the progesterone secretion to fall within 4 days. Thus it seems that the corpus luteum has a limited functional life span, and it normally requires the presence of a pituitary luteotrophin during the second half of the oestrous cycle if it is to secrete normally for 15 days. Pituitary stalk section early and late in the oestrous cycle. Regardless of the time of stalk section, the corpus luteum behaves as it would during a normal cycle. Thus pituitary stalk section does not produce the same effect as hypophysectomy, and seems to allow the severed pituitary gland to continue secreting luteotrophin. Hypophysectomy and hysterectomy carried out simultaneously early in the cycle. The results were similar to those in 1, progesterone secretion having declined significantly by days 12–15. This confirms that the declining secretory activity is due to a deficiency of pituitary luteotrophin, and not to any uterine luteolytic effect in this experiment. Pituitary stalk section and hysterectomy carried out simultaneously early in the cycle. In striking contrast to 3, some corpora lutea were still secreting progesterone normally on day 18. This shows once again that the isolated pituitary gland can continue to secrete luteotrophin. The different responses in this experiment and 2 emphasise the fact that the uterine luteolytic effect is normally dominant to the pituitary luteotrophic stimulus. Thus it would be impossible to demonstrate luteotrophic activity if the uterus were still present. Hysterectomy carried out at mid cycle, followed by hypophysectomy 20–30 days later. Whilst hysterectomy alone prolongs the secretory activity of the corpus luteum, subsequent hypophysectomy results in a rapid decline in progesterone secretion, commencing 48 hours after the operation. Thus the corpora lutea prolonged by hysterectomy, unlike those of the normal cycle, require daily pituitary luteotrophin secretion for their continued existence. Hysterectomy carried out at mid cycle, followed by pituitary stalk section 20–30 days later. Unlike 5, stalk section allows the corpora lutea to continue to secrete progesterone in large amounts for at least 15 days after the operation. This experiment, together with 2 and 4, once again emphasises that the stalk-sectioned pituitary gland can continue to secrete luteotrophin, at least for a time. These experiments therefore support the view that the cyclical corpus luteum of the sheep is under a dual control. There is a pituitary luteotrophin, whose secretion continues after stalk section, and a uterine luteolysin that is dominant to the luteotrophic stimulus, and can still function normally after pituitary stalk section. The fact that the corpus luteum of the hysterectomised animal cannot function for more than about 15 days after stalk section suggests that the luteotrophic stimulus may be complex, possibly envolving more than one hormone.


1987 ◽  
Vol 114 (2) ◽  
pp. 231-239 ◽  
Author(s):  
J. P. Hearn ◽  
G. E. Webley

ABSTRACT The interaction between luteotrophic and luteolytic agents in controlling progesterone production by the marmoset corpus luteum in the late luteal phase/early pregnancy was investigated at the local level in vivo using a perfusion cannula system. Perfusion of the prostaglandin F2α(PGF2α) analogue, cloprostenol (0·5 μg/ml), resulted in an immediate fall in progesterone production. This response was not sustained in two out of five corpora lutea but pregnancy was terminated in all animals exposed to PGF2α. Perfusion of human chorionic gonadotrophin (hCG) (4 μg/ml) alone significantly stimulated progesterone secretion but there was no response to hCG when the corpus luteum had previously been perfused with PGF2α. Perfusion with hCG together with PGF2α prevented a fall in progesterone secretion. The results suggest that the luteolytic action of PGF2α in the marmoset may be to prevent luteotrophic support of the corpus luteum. Melatonin (860 pmol/l), perfused either with PGF2α or after PGF2α, stimulated progesterone production. The ability of melatonin to influence progesterone production by the primate corpus luteum may therefore be by both a direct luteotrophic action and the prevention of luteolysis. Application of the perfusion system in order to investigate the ability of deglycosylated hCG to antagonize the action of hCG at the corpus luteum showed the necessity of testing pure preparations of hormones. J. Endocr. (1987) 114, 231–239


1972 ◽  
Vol 54 (1) ◽  
pp. 147-159 ◽  
Author(s):  
N. L. POYSER

SUMMARY The production of prostaglandins by the uterus and the resting levels of prostaglandins in the uterus on selected days of the oestrous cycle were determined in guinea-pigs. Prostaglandin F2α was detectable in the guinea-pig uterus in small amounts on days 13, 14 and 15 of the cycle. Prostaglandin E2 was present in even smaller amounts on days 14 and 15. The homogenized guinea-pig uterus had the ability to biosynthesize prostaglandins, from endogenous precursors, during incubation on every day of the cycle studied. Four to six times more prostaglandin F2α than E2 was produced on any one day with the amounts of prostaglandins formed increasing towards the end of the oestrous cycle. Indomethacin inhibited the biosynthesis of prostaglandins by the guinea-pig uterus. The implications of these findings are discussed.


1972 ◽  
Vol 55 (3) ◽  
pp. 599-607 ◽  
Author(s):  
B. T. DONOVAN ◽  
A. N. LOCKHART

SUMMARY The release of ovulating hormone after acute treatment with gonadal steroids, or corpus luteum removal on different days of the oestrous cycle, was studied in the guinea-pig. Injection of 25, 50 or 100 μg oestradiol or 2·5 mg progesterone on day 13 of the cycle had no effect upon gonadotrophin secretion as judged by follicular histology, but markedly altered the sizes of the corpora lutea of the previous ovulation. Treatment with oestradiol on day 14 did not elicit gonadotrophin secretion. However, administration of the same hormones to animals given 10 μg oestradiol benzoate 24 h earlier caused ovulation or follicular luteinization. Progesterone (2·5 mg) appeared least effective in stimulating gonadotrophin release; 25 μg oestradiol were more effective when given at 12.00 h than at 24.00 h but treatment with both hormones caused ovulation when given at either time of day. Luteal volumes were not affected. Removal of corpora lutea during the second half of the cycle advanced the time of expected ovulation to day 15 or earlier when the procedure was carried out on days 8 or 9, but not on days 10–13. It is concluded that 4–5 days must elapse between the fall in plasma progesterone level associated with corpus luteum regression and the release of ovulating hormone.


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