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Topic:Ovulation
Ovulation in horses is a physiological process involving the release of an ovum from the ovary, typically occurring during the mare's estrous cycle. This process is regulated by hormonal changes, primarily involving luteinizing hormone (LH) and follicle-stimulating hormone (FSH). Ovulation is a key component of equine reproduction, influencing breeding management and fertility outcomes. The timing and detection of ovulation are critical for optimizing breeding strategies, often involving techniques such as ultrasound examination and hormone assays. This page compiles peer-reviewed research studies and scholarly articles that investigate the mechanisms, detection methods, and implications of ovulation in equine reproductive health.
A preovulatory rise of dehydroepiandrosterone in the mare measured by radioimmunoassay. A radioimmunoassay procedure was developed for the measurement of dehydroepiandrosterone (DHA) in peripheral serum in nonpregnant mares. The synthesis and conjugation of 3beta-hydroxy-5-androsten-19-al-17-one 19(0-carboxymethyl) oxime is described. Antisera were developed against this antigen and characterized. The most specific antiserum was used to measure DHA. Concentrations of DHA were greatest immediately before ovulation.
Plasma luteinizing hormone concentration in mares treated with gondotropin-releasing hormone and estradiol. Three experiments were performed to study the luteinizing hormone (LH) and ovulatory responses to various doses and methods of administration of gonadotropin-releasing hormone (GnRH) in estrous pony mares and the influence of estradiol-17beta (E2-17beta) on LH response to GnRH treatment. In experiment 1, single injections of synthetic GnRH were subcutaneously given to 5 groups of estrous (day 2) mares (3 mares/group) on a body weight basis as follows: group A--isotonic saline solution; group B--GnRH, 0.14 mug/kg; group C--GnRH, 0.28 mug/kg; group D--KGnRH, 0.59 mug/kg; and group E--GnRH, 2.37 ...
A surgical technique applied to the study of tubal eggs in the mare. An efficient surgical technique of collecting eggs from the oviducts of mares is described. Within 6 days after ovulation recovery was successful in 22/29 mares. The technique has been used to investigate the retention and ageing of eggs in the oviducts and to determine the origin and the nature of the accessory CL during pregnancy.
Relationship between the morphology of and progesterone production by the corpus luteum of the mare. The histology of the growing, secreting and regressing CL of thirty-five cycling and early pregnant mares with known breeding histories was studied by light microscopy. Thecal cells are best developed a few days before ovulation. They regress very quickly and within 24 hr after ovulation all remaining thecal cells are in an advanced stage of degeneration. Hypertrophy and luteinization of the granulosa cells commences 10 hr after ovulation and maximum size (37-5 mum) is reached later. The luteal tissue enlarges mainly through hypertrophy of the lutein cells. Two types of lutein cells are found ...
A survey of eggs in the oviducts of mares. A total of 424 eggs was recovered from flushings of 176 pairs of oviducts. Of these eggs, 324 were in a state of advanced degeneration (Type 4) and ten appeared to have been recently ovulated (Type 1). The number of eggs/oviduct varied from 0 to 13, most being up to 3 eggs, but fifty oviducts contained no eggs. It is widely believed that unfertilized ova are selectively retained in the oviducts but an alternative explanation for their presence is put forward.
Effects of progesterone on reproductive function in mares after parturition. The injection of 100 mg of progesterone/day from Days 5 to 14 after foaling blocked or delayed oestrus and ovulation in 6/9 mares; the remainder ovulated during treatment without showing oestrus. Urinary oestrogen concentrations in these mares were highest between Days 9 and 15 after foaling but the peak levels were only about half those seen in untreated mares during the post-partum oestrus and ovulation. The injection of 200 mg progesterone/day blocked oestrus and ovulation in two mares but did not depress oestrogen excretion maxima any further. Follicles prevented from developing beyond a c...
The cycle of oestrus, ovulation and plasma levels of hormones in the mare. The duration of the oestrous cycle and day of ovulation were recorded in six mares which were used for concurrent assay of plasma levels of sex steroids and pituitary LH concentration. Peak of progesterone were reached during dioestrus and those of oestradiol and androstenedione occurred 2 days before ovulation and were in decline on the day of ovulation. Plasma oestrone remained constant (between 9 and 12 pg/ml) throughout the cycle. Plasma LH rose to a maximum near to the time of ovulation, and thereafter decreased gradually until mid-dioestrus. The pattern of secretion is compared with that...
The site of ovulation in the mare. Serial photography of the ovary of a mare by periodic surgical exteriorization of the ovary and peritonescopy in situ revealed that the ovulatory fossa is the site of ovulation in this species.
Oestrogen excretion in mares in relation to various reproductive states. The rate of urinary oestrogen excretion was studied in four ovariectomized mares. In two animals ovariectomized when urinary oestrogen concentration was high, levels fell to a minimun within 48 hr. Intramuscular injection of oestradiol-17beta produced maximum urinary oestrogen levels within 3 to 6 hr and a return to minimum detectable levels within 24 hr. The major urinary oestrogen in mares was oestrone. In nine maiden mares studied between September and June, the cycle, the durations of dioestrus and oestrus, and the time of ovulation were similar in autumn (September to December) and spring...
Duration of oestrus and time of ovulation in mares treated with synthetic Gn-RH (AY-24,031). Synthetic Gn-RH, administered during oestrus, stimulates the release of pituitary LH in the cyclic mare. Duration of oestrus was significantly reduced by 1 mg Gn-RH given on Day 2 of oestrus; the time of ovulation, measured in days from the onset of oestrus, also tended to be reduced. An injection of 2 mg Gn-RH had nor further effect, but daily injections from Day 2 until ovulation significantly shortened the duration of oestrus and the time to ovulation. The profiles of LH were found to be variable from mare to mare, but in all mares, treated and control, elevation of LH was detected close to...
Effects of artificial light on the oestrous cycle of the mare. Two groups, each of seven pony mares, were maintained from 17 October to 15 February (120 days) in the University Biotron where temperature and daily photoperiod were regulated to simulate normal conditions for that period (control group) or those normally applicable from 1 March to 1 July (treated group). Follicular growth, ovulation rate and oestrous behaviour were determined daily by rectal palpation, and by teasing with a stallion. By Day 69 of treatment, all ovarian end-points (number of follicles greater than 10 mm, number of follicles greater than 20 mm, average follicle diameter and di...
Influence of intrauterine saline infusion upon the oestrous cycle of the mare. The effect of intrauterine saline on reproductive function was studied by infusion of mares in anoestrus, dioestrus, oestrus and prolonged dioestrus. Anoestrous mares were unaffected except near the beginning and end of the breeding season when anovulatory heats were induced. Dioestrous mares infused between Days 5 and 9 returned to heat an average of 3-8 days earlier than expected, and infusions during dioestrus were followed by ovulatory heats of normal fertility. Three mares in prolonged dioestrus showed ovulatory heats within 3 to 9 days of infusion. Infusions during oestrus had no appreci...
Effects of prostaglandin F2alpha on the oestrous cycle and pregnancy in mares. Several experiments indicated that prostaglandin F2alpha (PGF2alpha) has luteolytic and abortifacient properties in mares. A single subcutaneous injection of 1-25 mg PGF2alpha on Day 6 of dioestrus was as effective as 10 mg PGF2alpha in inducing luteolysis. Oestrus and ovulation appeared to be synchronized when a single injection of 1-25 mg PGF2alpha was given on Days 7, 10 or 13 after ovulation but not on Days 1 or 4 after ovulation or on Day 2 of oestrus. Intramuscular administration was as effective as subcutaneous administration and 1-25 mg PGF2alpha was the minimal effective systemic dose...
Synchronization of oestrus in mares with a prostaglandin analogue and HCG. Following an initial observation period of 13 days when plasma progesterone levels were determined, synchronization of oestrus and ovulation was investigated in thirty-three mares treated with a prostaglandin analogue ('Equimate') and HCG. Two courses of treatment were given 8 days apart and each consisted of a single intramuscular injection of Equimate (250 mug) followed 6 days later by an intramuscular injection of HCG (2500 i.u.). The first course was designed to remove all luteal tissue and to induce ovulation of any follicles that developed in response to the withdrawal of progesterone. T...
Serum concentrations of FSH, LH and progesterone during the oestrous cycle and early pregnancy in the mare. Heterologous radioimmunoassays were developed for equine FSH and LH. Serum concentrations were measured in twenty-three mares throughout the oestrous cycle and early pregnancy. FSH concentrations were raised fivefold by 'surges' rather than 'spiked', occurring at 10- to 11-day intervals during the oestrous cycle and early pregnancy. The late oestrous/early dioestrous surge of FSH appeared to initiate development of up to twenty follicles. The mid-dioestrous surge may be important for the further development of follicles destined to ovulate 10 to 13 days later. Levels of LH were increasing by t...
The oestrous cycle of the mare. In eleven non-pregnant mares examined for 2 years, oestrous cycle length was 20-6 days (range 13 to 34) excluding any anoestrous periods. The duration of oestrus was 5-7 days (range 1 to 24); from February to May it was 7-6 days (range 2 to 24) and from May to November 4-8 days (range 1 to 10). The majority of ovulations occurred between 16.00 and 08.00 hours and 78% of the mares ovulated within 48 hr of the end of oestrus. Mean follicular diameter was 45 mm on the day of ovulation and there was a 25-5% incidence of multiple ovulations. It was uncommon for oestrus to occur without ovulation, w...
The use of Gn-RH for controlling the oestrous cycle of the mare (preliminary report). Clinical tests with synthetic gonadotrophin-releasing hormone (Hoechst) were made during the breeding seasons of 1973 and 1974, using 128 mares injected with 1-0 to 4-0 mg of the substance intramuscularly. The mares were placed in one of five groups based on ovarian condition determined by clinical evidence. Some success was obtained in the induction of ovulation in mares with inactive and sub-normally active ovaries and in a small group having cystic ovaries. A large proportion of mares having a mature follicle responded within 48 hr, but others with atretic follicles failed to respond. The u...
The use of prostaglandin F2alpha in controlling the oestrous cycle of the mare and steroid changes in the peripheral blood. Prostaglandin F2alpha (PGF2alpha), administered by untrauterine infusion and intramuscular injection, was used to induce oestrus and ovulation in non-cyclic mares. A satisfactory response rate (80% or more) was obtained and the dose (2-5--7-5 mg) and the time taken for ovulation to occur (up to 9 days) was the same irrespective of the route of administration. Only about one-half of the mares conceived to mating at the induced oestrus but the low conception rate could be attributed to the infertile condition of the mares. Plasma progesterone remained at basal levels after PGF2alpha and oestroge...
Urinary oestrogen and plasma progesterone levels in non-pregnant mares. Eight mares were observed clinically for 14 months to detect oestrus and ovarian activity, and assays of urinary oestrogens and plasma progesterone were performed. Cyclical ovarian activity occurred during 60% of the experimental period. Persistent luteal activity was found over 20% of the period and for the rest of the time activity was absent. Cyclical activity was characterized by the alternation of periods of low and high progesterone levels corresponding to the follicular and luteal phases of the ovarian cycle. During the follicular phase, urinary oestrogen levels increased to a maximum o...
Plasma LH levels in the mare during the oestrous cycle. Plasma levels of LH were determined by heterologous radioimmunoassay utilizing highly purified equine LH as standard. Samples were taken regularly from eleven mares for twenty-six oestrous cycles over a period of 10 weeks. The mean cycle length was 20-5 +/- 3-1 (S.D.) days, and ovulation occurred on average 4-3 +/- 1-6 (S.D.) days from the time heat was first detected. Levels of LH were persistently low from Days 5 to 16 of the cycle (ovulation = Day 0). They then increased slowly over a number of days and continued to rise beyond the levels observed at any time during the immediate preovulato...
The influence of intrauterine saline infusion on luteal function and cyclical activity in the mare. Intrauterine saline infusion in the dioestrous mare shortened the ovulatory interval by inducing premature luteolysis. Plasma progestagen levels began to decrease approximately 1 day after the infusion and had declined to less than 1-0 ng/ml in 4 days. The CL, including others formed from ovulations during dioestrus, must be 4 to 5 days old before intrauterine saline will induce luteolysis. Of 10 mares infused on Day 4 or 5 after ovulation, only six had a shortened ovulatory interval. Of 10 mares infused on Day 6 or 7 after ovulation, seven had a shortened ovulatory interval and three failed t...
The effect of HCG on duration of oestrus, ovulation time and fertility in mares. Two experiments were conducted to determine the effects of HCG on duration of oestrus, dioestrus, the length of the oestrous cycle, the time of ovulation and fertility in non-lactating mares. In the first experiment, the injection of HCG was repeated for three successive cycles. Mares injected with 2000 i.u. HCG on Day 2 of oestrus during their first cycle had a shorter oestrus and ovulated sooner than untreated control mares, but in the third cycle, treated mares had a longer oestrus and ovulated longer after the onset of oestrus than controls. In the second experiment, one intramuscular inje...
Relationship between luteal function and metabolic clearance and production rates of progesterone in the mare. The functional activity of the equine CL was measured by its ability to convert [4-14C]3beta-hydroxy-5-en-20-one to [4-14C]pregn-4-en-3,20-dione. The capacity of homogenates of CL of different ages followed the temporal pattern of plasma progestagen concentrations. In ten mares which ovulated twice at intervals of 0 to 9 days in the same cycle, the conversion capacity of the CL from the second ovulation was similar to that from the first ovulation. After adjusting for age, the CL from the first of two ovulations had a similar conversion capacity as that resulting from a single ovulation. Plasm...
Oestrus, ovulation and plasma hormones after prostaglandin F2alpha in mares. The luteolytic effect of PGF2alpha, administered by intrauterine infusion or subcutaneous injection during early dioestrus, was observed in mares of mixed breeds. An infusion of 10 mg on Days 7 to 9 after ovulation caused a sharp fall in plasma progesterone levels and induced oestrus and ovulation. Oestrus was significantly longer than in the natural cycle but the time of ovulation in relation to the end of oestrus was normal. The time of return to oestrus following luteolysis was not dependent on the amount of PGF2alpha within the range of doses given. Luteolysis could be induced as early as ...
Effect of photoperiod on reproductive activity and hair in mares. The effects of photoperiod on reproductive activity and hair changes in pony mares were studied in 2 experiments. In experiment I, the effect of a fixed daily photoperiod on the onset of the breeding season was studied in 36 mares from Nov 13, 1973, to June 13, 1974. The 4 treatment groups were as follows: daily photoperiod equivalent to the normal day length (control group); constant light 24 hours a day with no dark (L24:D0 group); 16-hour daily photoperiod with 8 hours of dark (L16:D8 group); and 9-hour daily photoperiod with 15 hours of dark (L9:D15 group). The intervals from beginning of ...
The use of prostaglandin F2alpha-tham salt in mares in clinical anoestrus. Seventy-three Standardbred and Thoroughbred mares in clinical anoestrus during the breeding season were treated with PGF2alpha. The mares were divided into four categories; foaling, barren, maiden and unknown. The response was consistent in all groups. Mares at Days 2 to 4 of dioestrus showed no decrease in plasma progesterone levels, and those at Days 6 to 8 showed a return of progesterone to baseline levels (less than 1 ng/ml) in 24 to 48 hr after treatment. Plasma progesterone levels returned to basal levels in 24 to 48 hr in 93% of mares; progesterone levels had not changed by 96 hr in 7% ...
Levels of LH, prolactin and oestrogens in the serum of post-partum mares. The levels of LH, prolactin and oestrogen were measured by radioimmunoassay in serum obtained from six mares during the post-partum period, and LH was also assayed in blood samples collected at 6-hr intervals from four normal cyclic mares during oestrus and at daily intervals during dioestrus. The concentrations of oestrogen and LH suggested that the mares were having ovulatory cycles during the post-partum period irrespective of behavioural oestrus, and the levels of prolactin seemed to rise in association with probable ovulatory LH peaks. In these mares levels of LH had increased significant...
Periovulatory changes in peripheral plasma progesterone and estrogen concentrations in the mare. Concentrations of progesterone and estrogen were measured in peripheral blood plasma samples from mares around the time of ovulation. Samples were collected every 2 hours from 36 hours before, to 26 hours after, ovulation and assayed by radioimmunoassay. Progesterone concentrations were between 60 and 100 pg/ml for the period 24 hours before ovulation through 8 hours after ovulation. By 10 hours after ovulation, concentrations increased to 140 pg/ml and, by 26 hours after ovulation, reached 346 pg/ml. Plasma estrogen concentrations did not change significantly throughout the same period.
