Peripheral plasma prolactin and progesterone levels in pseudopregnant goats during bromocryptine treatment

Persistence of luteal function and accumulation of fluid within the uterus (hydrometra) are characteristics of pseudopregnancy in goats. To study the luteotrophic role of prolactin in this condition, seven seudopregnant goats were treated with bromocryptine (1 mg subcutaneously, twice daily) for 6 to 10 d. Plasma progesterone (P4) and prolactin (PRL) were measured by radioimmunoassay (RIA) in samples taken twice daily by venipuncture. Ultrasound scanning took place at regular intervals to visualize the presence of fluid within the uterus. Bromocryptine treatment effectively reduced the plasma PRL concentration in six goats. In all seven goats, a gradual decrease of the plasma P4 concentration to levels < 1.8 ng/ml occured during treatment. After bromocryptine treatment, P4 concentrations reached basal levels (<0.1 ng/ml) in two animals. In four goats, P4 concentrations remained close to 1.0 ng/ml, or even temporarily rose above the 2.0 ng/ml level. Spontaneous discharge of uterine fluid took place during (two goats) or within 4 d after bromocryptine treatment (three goats). These results indicate that prolactin plays an important luteotrophic role during pseudopregnancy in goats.     

Peripheral plasma levels of progesterone in pregnant goats and in pregnant goats treated with prostaglandin F2a

Prostaglandin or prostaglandin analogues have been shown to be luteolytic in the pregnant goat. In this study the temporal changes in the plasma concentrations of progesterone during pregnancy and after administration of PGF2a to pregnant goats are described. PGF2a administration to pregnant goats at 30 and 65 days after breeding induced abortion within 34 to 75 hours. These abortions were accompanied by estrus and profuse muco-hemorrhagic discharges. When PGF2a was administered to pregnant goats 140 or 142 days after breeding, premature parturition occurred within 42 to 76 hours. Live kids were delivered in all cases. The plasma levels of progesterone in all pregnant goats showed dramatic decreases within 24 hours after the prostaglandin injections and continued to decrease gradually until abortions or premature parturition. Thereafter, the progesterone levels remained low for several days.     

Fertility and blood progesterone levels following LHRH-induced superovulation in FSH-treated anestrous goats

Twenty mature, mixed-breed, seasonally anestrous female goats were used to study the effects of luteinizing hormone releasing hormone (LHRH) on ovulation rate, fertility, and blood progesterone levels following norgestomet-induced estrus and follicle stimulating hormone (FSH) treatments. Each goat received 6 mg norgestomet by subcutaneous (sc) implant and 3 mg intramuscularly, along with an intramuscular (im) injection of 5 mg estradiol valerate. Four injections of FSH were given for 2 d in divided doses of 10, 10, 5 and 5 mg im every 12 h, starting at 24 h before implant removal. The goats were randomly assigned to 1 of 2 equal treatment groups, and were treated with 2 intravenous (iv) injections of either 0.9% saline (control) or 300 ug LHRH at 24 and 48 h after the removal of the implants. All the goats exhibited estrus within 24 or 36 h of implant withdrawal and were mated to bucks of proven fertility. At laparotomy on Day 7 or 8 after the removal of the implants, the mean number of unovulated follicles was higher (P<0.05) in Group I than in Group II. The mean number of corpora lutea (ovulation rate), the total number of embryos and the number of normal embryos recovered were higher (P<0.05) in LHRH-treated does than in the controls. Treatment with LHRH resulted in 72.14% fertility (mean number of CL = 14) as compared with the controls with 64.29% fertility (mean number of CL = 2.8). The embryos obtained from goats in Group II were of more uniform developmental age regardless of the day of embryo collection, as compared with those of the controls. Plasma progesterone levels were significantly increased on Days 4 to 6 in both treatment groups. The results of this study have demonstrated that the FSH and LHRH treatment regimen increased follicular development, ovulation rate and blood progesterone levels in norgestomet-treated anestrous goats. Moreover, LHRH treatment enhanced fertility, and improved embryo quality as indicated by the significantly higher total number of embryos as well as the higher (P<0.05) number of normal recoverable embryos.     

Peripheral plasma levels of certain mineral elements in primitive African goats

Changes in blood plasma calcium, inorganic phosphorus, magnesium, zinc, iron, copper, sodium and potassium concentrations over a 3-year period were investigated in primitive goats. Blood plasma mineral concentrations were determined by atomic absorption and a colorimetric method. Changes in Zn and Ca concentrations are season dependent, potassium levels show only a long-term change tendency, and magnesium and inorganic phosphorus had constant levels throughout the investigation period. Iron, copper and sodium showed both long-term change tendencies and more or less marked season related changes.     

The relationship of circulating plasma progesterone levels and rectal temperatures in gilts

To ascertain if a correlation exists between circulating plasma progesterone levels and rectal temperatures in swine, 10 mixed breed postpubertal ovariectomized gilts were treated with sesame oil containing 500 mg progesterone IM or with saline IM. The average daily rectal temperatures were not correlated with the circulating plasma progesterone levels. Rectal temperature observations do not provide a useful indication of corpus luteum activity in swine.     

Peripheral plasma levels of progesterone in goats treated with fluorogestone acetate and prostaglandin F2α during the estrous cycle

Intravaginal pessaries impregnated with 20 mg fluorogestone acetate (FGA) were inserted into fifteen does at various intervals after the end of estrus. After resumption of cyclical activity following withdrawal of the intravaginal pessaries, the does were divided into six groups and treated with prostaglandin F2_α. Each doe received 15 mg Prostaglandin F2_α administered intramusuclarly 2, 4, 6, 12, 14 or 16 days after the end of estrus. The animals were bred naturally on the first estrus following prostaglandin treatment. Jugular blood samples were collected from each doe throughout the experimental period. The plasma samples were assayed for progesterone. Intravaginal fluorogestone acetate treatment in does had no effect on the function of the corpus luteum, however, overt estrus was postponed during treatment and for a few days after removal of the pessaries. Prostaglandin injection into does, 4, 6, 12, 14 or 16 days after the end of estrus induced luteolysis and subsequent ovulatory estrus within 2 to 3 days. Fertility at PGF2_α induced estrus in these does was 77%. Prostaglandin treatment two days after the end of estrus had no effect on the corpus luteum function. It is concluded that prostaglandin is luteolytic when administered into does anytime beyond four days after the end of estrus.     

Ovarian activity and peripheral plasma levels of oestrogens and progesterone in the lactating sow

Ten gilts were examined for peripheral plasma levels of progesterone and oestrogens 3 weeks before and up to 8 weeks after parturition. The sows were slaughtered at different intervals after parturition and the ovaries were examined. Peripheral plasma levels of progesterone decreased dramatically from about 8ng/ml two days before parturition to about 2 ng/ml on the day before parturition. After parturition the mean progesterone level was about 1.5 ng/ml. Maximum oestrone levels of about 7 ng/ml were obtained two days before parturition. After parturition the level dropped to below 0.1 ng/ml. Three sows showed high levels of oestradiol (75–440 pg/ml) without signs of heat during the lactation. In no case were ovulated follicles or periodic corpora lutea registered.     

Peripheral plasma testosterone levels in two indian breeds of goats and their reciprocal crosses

Plasma testosterone levels were estimated in different male goat age groups. In Black Bengal at 15–30 days, 2–3 months, 3–5 months and in Black Bengal, Beetal, Beetal × Black Bengal and Black Bengal × Beetal at 6 months and > 12 months (n = 6 in each case). The plasma testosterone levels (mean ± s.e.m.) were high (7.1 ± 2.0 ng/ml) at 2–3 months and fell drastically to 2.6 ± 0.5 ng/ml before attaining sexually mature levels of 4.6 ± 0.9 ng/ml at 6 months and 4.1 ± 0.8 ng/ml at > 12 months. The mature bucks of all genetic groups had a plasma testosterone concentration of 4.6 ± 0.8 ng/ml. Genetic group differences were not significant.     

The effect of progesterone implants on ovulation and plasma levels of LH, FSH and progesterone in anoestrous ewes.

The effects of 100-mg progesterone implants in anoestrous ewes on plasma progesterone and gonadotrophin levels are described. Implant removal resulted in a surge of plasma gonadotrophins and ovulation, but there was no evidence of behavioural oestrus in 90% of the ewes. These results are discussed.     

Seasonal variations in post-partum plasma progesterone levels and conception in primiparous and multiparous dairy cows

Progesterone concentrations in peripheral plasma of 18 primiparous and 34 multiparous dairy cows were determined by radioimmunoassay every 4 days, from 10 days post partum until the next conception. The interval from parturition to the first progesterone peak (greater than 4 ng/ml plasma) was significantly longer (P less than 4 ng/ml plasma) was significantly longer (P less than 0.01) in primiparous than in multiparous cows. The progesterone concentrations on Days 4-15 of the oestrous cycle were significantly lower (P less than 0.025) during the summer than in cycles occurring in winter. The conception rate during the summer was lower than in winter. In cows inseminated in summer, conception was related to the shape of the progesterone curve in the cycle preceding insemination.     

Milk fat progesterone concentrations in goats and early pregnancy diagnosis

Blood and milk samples from foremilk during afternoon milking, were simultaneously collected from 285 dairy goats. In experiment 1, fiva cyclic goats were sampled daily for 21 days. In experiment 2, 280 females from 9 flocks were submitted to sampling 21 days after insemination. In addition, some milk samples were divided in two parts, after which one was frozen and the other kept at +4 degrees C until assay. Progesterone concentrations were measured in blood, whole milk and milk fat by radioimmunoassay. No difference in whole milk or fat progesterone levels was found between frozen and refrigerated milk samples. Milk butterfat progesterone concentrations paralleled those in plasma or whole milk throughout the estrous cycle and ranged from about 20 ng/ml at estrus to about 400 ng/ml in mid-luteal phase. The ratio of mid-luteal phase progesterone levels to those seen in the estrous period was over 20 in fat and in blood. This ratio was very much lower in whole milk. Consequently the determination of pregnant and non-pregnant goats from the samples collected 21 days after service was very much easier and accuracy was better when the progesterone content was assayed from milk fat than from whole milk. It was concluded that early pregnancy diagnosis in goats can be done routinely by determination of progesterone levels in milk fat.     

Ovarian and luteal blood flow, and peripheral plasma progesterone levels, in cyclic guinea-pigs

Ovarian and luteal blood flow rates were studied using radioactive microspheres in guinea-pigs between Day 6 of the oestrous cycle and Day 1 of the following cycle. Peripheral plasma progesterone levels were measured by radioimmunoassay on the same days of the oestrous cycle. Ovarian blood flow was greatest between Days 9 and 12 and had fallen by Day 16 both in absolute (ml . min-1) and relative (ml.min-1.g-1) terms. Luteal weight and blood flow were also greatest between Days 9 and 12 and had fallen sharply by Day 16. The highest mean (+/- s.d.) luteal flows measured were 0.10 +/- 0.04 ml.min-1 per corpus luteum, and 24.26 +/- 9.3 ml.min-1.g-1 luteal tissue on Day 10 of the cycle. Mean peripheral plasma progesterone levels reached a maximum of 3.66 +/- 1.1 ng/ml at Day 12 of the cycle and fell thereafter, reaching 0.74 +/- 0.5 ng/ml by Day 1 of the following cycle. Plasma progesterone levels declined significantly between Days 12 and 14 of the cycle, whereas no significant drop in luteal blood flow was demonstrable until after Day 14. These data do not support the idea that declining luteal blood flow is an initiating mechanism in luteal regression in the guinea-pig.