Lars-Eric Edqvist

Post-partum release of prostaglandin F2α and uterine involution in the cow

Peripheral plasma levels of the main blood plasma metabolite of PGF2α (15-keto-13,14-dihydro-PGF2α) and progesterone were investigated during the immediate, post-partum period in 59 normally calving cows. Uterine involution was monitored by weekly rectal palpations. The levels of the prostaglandin metabolite were high at parturition and remained thereafter elevated for periods varying up to 7–23 days. Uterine involution was completed during periods ranging from 16–53 days. According to the clinical findings, the animals were divided into three groups. Group A comprises 46 animals which had an uncomplicated, puerperal period. A significant (p<0.001) correlation between the duration of elevated prostaglandin levels and the time for completed uterine involution (Y=29.6 − 1.3 (X − 13.5)) was found for these animals. Group B animals (n=8) had periods of varying length with uterine discharge during the first 30 days post-partum. When compared to group A animals, the animals in group B had comparatively longer periods of prostaglandin release and also longer periods for completion of uterine involution. Group C animals (n=5) at times had palpable, thin-walled, cystlike structures in the ovaries during the first 30 days post-partum. In this group of animals, the periods of high prostaglandin levels, as well as for the completion of uterine involution, were similar to those for the animals in group A. Progesterone levels remained low during the immediate post-partum period and in no case were elevated levels found until the prostaglandin release had ceased.

Blood levels of 15-keto-13, 14-dihydroprostaglandin F2α during the postpartum period in primiparous cows

Plasma levels of the PGF(2alpha) metabolite 15-keto-13, 14-dihydroprostaglandin F(2alpha) were determined postpartum in 51 primiparous Black and White Lowland cows. The highest geometric mean was 1702 pmol/l on day 3 and lowest 190 pmol/l on day 21. It should be noted that variation between animals in the concentration of the metabolite is high. For instance, on days 4, 10, 16 and 22, concentration of metabolite ranged from 775-2500, 209-2450, 45-851 and 30-398 pmol/l, respectively. The duration of the massive postpartum release of PGF(2alpha) could be determined in only 29 cows. Significant correlations were found between the duration of elevated PGF(2alpha) metabolite levels and the time required for completion of uterine involution (r = -0.41, P < 0.05) and between the duration of increased PGF(2alpha) metabolite levels and the interval from parturition to occurrence of the first ovulation followed by a normal luteal phase length (r = -0.37, P < 0.05). The occurrence of the first ovulation followed by a normal luteal phase length in the 29 cows was positively correlated with the time needed for completion of uterine involution (r = 0.54, P < 0.01).

Endocrine profiles and embryo quality in the PMSG-PGF2α treated cow

Plasma progesterone and LH concentrations around estrus were determined for both PMSG treated (experimental animals) and non-treated (control animals) dairy cows and heifers of the Holstein Friesian and Jersey breeds, and these hormone profiles were related to the embryo quality. Most experimental animals experienced an increase in progesterone concentrations following PMSG treatment and an abrupt decrease to values below 3 nmol/l after PG injection. The mean (+/-SE) intervals from prostaglandin treatment to estrus were 46.9+/-1.8 h and 64.5+/-4.8 h for experimental and control animals, respectively. At the onset of heat the progesterone concentration in experimental animals with optimal embryo quality (group I) was significantly lower (p<0.01) than in experimental animals which yielded unfertilized eggs (group II) (1.2+/-0.1 versus 3.9+/-0.8 nmol/l) and significantly higher than the level in the control group (0.6+/-0.1 nmol/l). Following estrus the progesterone profiles in all 3 groups were studied and the length of the superovulatory cycle was measured to 26.0+/-4.8 days. The preovulatory LH surge occurred sooner after prostaglandin injection in experimental (41 h) than in control animals (65 h). The LH surge in group I occurred within a narrow range and reached a higher average level than group II (24.2+/-2.2 ng/ml and 16.3+/-3.7 ng/ml, respectively). The control group attained an even higher LH surge (31.8+/-8.8 ng/ml) than did the experimental animals. The data presented in this experiment indicate that plasma levels of progesterone and LH in PMSG-PGF2alpha treated animals are related to embryo or egg quality.

Endotoxin-induced prostaglandin release and corpus luteum function in goats☆

Abstract Endotoxin (lipopolysaccharide) from Salmonella typhimurium was administered to non-pregnant and pregnant goats to investigate its capacity to induce synthesis and release of prostaglandin with subsequent alteration of reproductive functions. Prostaglandin release was determined by measurement of 15-keto-13,14-dihydro-PGF 2α and the corpus luteum function was monitored by measurement of progesterone. Endotoxin administered into the lumen of the uterus did not alter the hormonal patterns. However, when 1.8 μg/kg of the endotoxin was given i.v., a rapid increase of 15-keto-13,14-dihydro-PGF 2α and a subsequent decline in progesterone levels were seen. Both non-pregnant and hysterectomized animals shortened their lengths of oestrous cycles. In two out of three pregnant animals the i.v. administration of the endotoxin (0.1 μg/kg) resulted in abortions. When comparing the prostaglandin metabolite response of intact vs. hysterectomized animals, the response was somewhat less in the latter group. When endotoxin was administered in smaller amounts (0.5 μg/kg) to non-pregnant goats it created an immediate increase in prostaglandin metabolite levels, but the subsequent decline in progesterone levels was less pronounced and the length of the oestrous cycle was not altered. From the present study it is obvious that i.v. administered endotoxin can influence the life-span of the corpus luteum, which is probably mediated by induction of synthesis and release of PGF 2α .

Attainment of puberty in female pigs: Clinical appearance and patterns of progesterone, oestradiol-17β and LH

Abstract The object of the study was to investigate the clinical and endocrine patterns of progesterone, oestradiol-17β and LH during the peripubertal period in female pigs. Crossbred gilts were penned in groups at an age of 10–12 weeks and boars were kept in adjacent pens during the entire experimental period. Daily oestrous checks started at 4.5 months of age and the gilts were slaughtered after their third heat. At the age of 4.5–5 months a permanent catheter was inserted in the cephalic vein and blood samples were collected from the gilts once daily until either the first or second oestrus. In three gilts hourly blood samples were taken during their first and second oestrus, beginning at early pro-oestrus. The gilts showed their first oestrus at the average age of 183 days. No corpora lutea from earlier ovulations were observed in gilts laparoscoped after their first detected oestrus. During the 30-day period before first oestrus the mean daily progesterone levels varied between 32 and 329 pmol/l. The average levels of oestradiol-17β varied between 15.6 and 30.8 pmol/l. There was no tendency for the oestradiol-17β level to rise before onset of first pro-oestrus. The average levels of LH varied between 0.15 and 0.94 μg/l. The statistical analyses revealed no significant relationship between the level of the hormones studied and onset of first oestrus. The mean progesterone levels during the first and second oestrous cycles were almost identical, however. Oestradiol-17β increased gradually during pro-oestrus, reaching maximum levels before onset of oestrus and thereafter decreasing sharply to values around 30 pmol/l. The oestradiol-17β levels were higher at the second than at the first pro-oestrous period. The concentrations of plasma LH rose sharply with declining plasma levels of oestradiol-17β. The duration of elevated plasma LH levels (> 1 μg/l) was, on average, 26 h and the LH levels were higher during the first oestrus than during the second oestrus. The first rise in progesterone was observed 11–29 h after the LH levels had decreased to concentrations below 1 μg/l.

Plasma progesterone levels from oestrus through day 7 after A.I. in heifers carrying embryos with normal or deviating morphology

Twenty-five dairy heifers, 11 repeat breeder and 14 virgin heifers, were used. Blood samples were taken twice a day (9 a.m. and 3 p.m.) from day of A.I. to 7 days later when embryo collection was made. One series of blood samples were taken from 16 heifers and two and three, respectively, from 6 and 3 heifers. Analysis of progesterone was performed by radioimmunoassay. The embryos were classified in 3 groups: normal blastocysts, morphological deviators, and degenerated embryos. Analysis of variance and a discriminant analysis was performed. The discriminant analysis was made to predict embryonic morphology, using daily progesterone values as predictors. No significant relationship between embryonic morphology and progesterone levels was found. The discriminant analysis showed that 64.9 % of progesterone curves were correctly classified, with individual groups ranging from 50 % (degenerated) to 76.5 % (normal embryos). It was concluded that abnormal embryonic development occurs with normal lateal function and that normal bovine embryo does not exhibit luteotrophic activity 7 days after mating.

Prostaglandin induced early abortions in the bovine. Clinical outcome and endogenous release of prostaglandin F2α and progesterone

Abstract Peripheral blood plasma levels of progesterone and the main blood plasma metabolite of prostaglandin F2α (15-keto-13, 14-dihydro-PGF2α) were analysed in 12 heifers in which abortions were induced with a prostaglandin analogue (cloprostenol) at pregnancy stages from 39–146 days. All animals except one (treated on day 75 of pregnancy) aborted within 4 days following treatment. The peripheral plasma levels of progesterone decreased rapidly following the injection of cloprostenol. All heifers had shortlasting peaks of the prostaglandin metabolite in connection with luteal regression. In animals pregnant for less than 80 days this release ceased at the time of delivery of the fetuses, which were expelled within unruptured fetal membranes. Standing estrus was observed in connection with the expulsion of the fetuses. Two of the animals were mated at this estrus and became pregnant. In contrast, animals pregnant for more than 100 days released massive amounts of prostaglandin F2α during a 2–5-days period post partum and had retained fetal membranes. No heat was observed in connection with these abortions. The animal that failed to abort showed no change in the prostaglandin metabolite levels.

On the control of prostaglandin release during the bovine estrous cycle. Effects of progesterone implants.

Progesterone implants were inserted subcutaneously on day 12 of the estrous cycle in three heifers. The implants were known to release an amount of progesterone sufficient to maintain the peripheral blood plasma at a level of about 1 ng/lm. All three heifers showed luteolysis in a similar way with peaks of 15-keto-13, 14-dihydro-PGF2 alpha of normal magnitude and duration. Concomitantly, progesterone levels declined, but due to the presence of the implants, progesterone was maintained at a level of about 1 ng/ml. The release of prostaglandins, however, continued throughout the experimental period and did not cease until the implants were removed.

11-Ketotetranor PGF metabolites, a suitable indicator for measuring prostaglandin release during the normal oestrous cycle and early pregnancy in the goat

Abstract Peripheral plasma levels of 15-ketodihydro-PGF2α, 11-ketotetranor PGF metabolites and progesterone were measured during normal oestrous cycle and early pregnancy in six goats. The does were synchronized before the start of the study by means of 10 mg of PGF2α. Blood samples were collected twice daily until day 12 of the oestrous cycle and subsequently every 3 h until the onset of oestrus, at which time the does were mated. The blood sampling protocol was repeated until day 28 of pregnancy. High pulsatile peaks of 15-ketodihydro-PGF2α and 11-ketotetranor PGF metabolites were observed during the last days of the oestrous cycle, indicating PGF2α releases. This coincided with a fall in progesterone levels. During early pregnancy no such peaks of prostaglandin metabolites were recorded and high levels of progesterone were maintained. In the goat, analysis of the 11-ketotetranor PGF metabolites seems to be a better indicator of PGF2α release than the analysis of 15-ketodihydro-PGF2α. The former metabolites are more long-lived in the circulation and are thus easier to detect.

Progesterone determinations and clinical examinations of reproductive organs in purebred and crossbred female zebu cattle.

Five experiments were undertaken to investigate variation in progesterone concentrations as related to the collection and handling of samples of milk and blood, to determine reference values for progesterone and to evaluate clinical findings in relation to progesterone data from pure- and crossbred Zebu cattle reared in the Peruvian tropics. Whole-milk progesterone concentrations obtained from 12 Holstein x Nellore pregnant cows at hourly intervals over a 24-h period were highest immediately after milking; this peak was followed by a sharp drop over the next 3 h. Milk-fat content from 28 Brown Swiss x Nellore pregnant cows increased from 2.4% before milking to 6.7% afterwards (P < 0.05), whereas progesterone concentrations in whole milk increased from 18.4 to 59.5 nmol/1 (P < 0.05). Progesterone concentrations in fat-free milk were stable, with the exception of the fore-milk sample, which was lower than subsequent samples collected during milking (P < 0.05). Blood samples collected from 23 purebred, pregnant Nellore cows, were divided into four aliquots, and plasma and serum were harvested periodically over the next 120 h of storage at +4 degrees C, or in the shade at ambient air temperatures. The results indicate that blood samples can be stored unseparated at both temperatures studied for up to 3 h without severe loss of progesterone. Milk samples collected at different intervals during the luteal phase of the estrous cycle and during early and mid-pregnancy from crossbred cows showed no significant differences in progesterone concentrations between Days 9 to 13 of the cycle and Days 9 to 13 of gestation. Progesterone levels during advanced gestation were higher (P < 0.05). Out of 2,607 clinical examinations, the level of agreement between palpatory findings and progesterone determinations was 95.6 and 81.9% in diagnosing non-luteal and luteal structures, respectively. Significant differences in the level of agreement between palpators were found (P < 0.01). It is concluded that milk samples, preferably composite milk or strippings, must be consistently collected at the same stage of milking, and that centrifugation of blood samples should be done as soon as possible and not later than 3 h after collection.