The estrous cycle in horses is a recurring reproductive cycle that mares undergo, typically during the breeding season. This cycle is characterized by a series of hormonal changes that prepare the mare for potential conception. The cycle is divided into two main phases: estrus and diestrus. During estrus, the mare is receptive to mating, and ovulation occurs. In contrast, the diestrus phase is a period when the mare is not receptive to a stallion. The regulation of the estrous cycle involves a complex interplay of hormones such as estrogen, progesterone, luteinizing hormone, and follicle-stimulating hormone. Understanding the estrous cycle is important for effective breeding management and reproductive health in horses. This page compiles peer-reviewed research studies and scholarly articles that explore the physiology, hormonal regulation, and implications of the estrous cycle in equine reproduction.
Hillman RB, Loy RG.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...
Parker WG, Sullivan JJ, First NL.Fifty mares were inseminated on Days 2, 4, 7, 11 or 17 of the oestrous cycle with spermatozoa from one of three stallions to observe the distribution of the spermatozoa in various parts of the reproductive tract 12 hr later (Days 3, 5, 8, 12 and 18). Only 0-06 to 2-21% of inseminated spermatozoa were recovered from the tract. More (P less than 0-05) spermatozoa were recovered from the cervix and uterus on Day 12 than on Days 3, 5, 8 and 18. The mean number of spermatozoa recovered from either or both oviducts was significantly greater (P less than 0-10) on Days 5 and 8 than on Days 3, 12 and 1...
Sharp DC, Kooistra L, Ginther OJ.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...
Arthur GH.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...
Evans MJ, Irvine CH.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...
Hughes JP, Stabenfeldt GH, Evans JW.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...
Heinze H, Klug E.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...
Voss JL, Pickett BW.The effect of rectal palpation of fertility of non-lactating, normal cyclic mares was studied over 3 years. During the first year (1971), the conception rates in mares after daily paplaption during oestrus only, and during oestrus and the first 50 days of pregnancy, were not significantly lower (P greater than 0-05) than the conception rates recorded in mares not palpated. No abortions could be attributed to palpation. Oestrus lasted longer (P less than 0-05) in non-palpated than palpated mares. During the second year (1972), first-cycle pregnancy rates in two groups of mares palpated daily du...
Spincemaille J, Coryn M, Vandekerckhove D, Vandeplassche M.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...
Palmer E, Jousset B.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...
Geschwind II, Dewey R, Hughes JP, Evans JW, Stabenfeldt GH.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...
Neely DP, Hughes JP, Stabenfeldt GH, Evans JW.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...
Ganjam VK, Kenney RM, Flickinger G.The pattern of plasma progestagen levels during the oestrous cycle was similar to that previously reported except for lower peak levels. The lack of significant difference (p less than 0-01) between CPBA and RIA values suggests that progesterone itself is the major component during the oestrous cycle. Progesterone levels during the first and second post-parturient oestrous cycles were similar to those observed during the cycle of the non-pregnant mare. During pregnancy there were two peaks of plasma progestagens. The first, which occurred during the 3rd month, coincided with high levels of PMS...
Voss JL, Sullivan JJ, Pickett BW, Parker WG, Burwash LD, Larson LL.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...
Hay MF, Allen WR, Lewis IM.Graafian follicles of various sizes obtained from mares at different stages of the oestrous cycle were examined histologically and histochemically for delta5-3beta-hydroxysteroid dehydrogenase (3beta-HSD) activity and related enzymes. The 3beta-HSD activity was not found in the theca interna of any follicles but was present in the membrana granulosa of well-vascularized large follicles in the late luteal phase of the cycle and at oestrus. These findings indicate that pregnenolone cannot be converted into progesterone in the theca interna. It is suggested that this conversion occurs in the memb...
Oxender WD, Noden PA, Hafs HD.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 ...
Kooistra LH, Ginther OJ.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 ...
Kenney RM, Ganjam VK, Cooper WL, Lauderdale JW.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% ...
Oxender WD, Noden PA, Bolenbaugh DL, Hafs HD.To determine the minimal effective dose of prostagiandin (PGF2alpha; tromethamine salt) given subcutaneously (SC), mares of mixed breeding (400 kg av body weight) were given 2-, 3-, 5-, and 10-mg doses from 7 to 9 days after ovulation. In some but not all mares given doses of 2 and 3 mg of PGF2alpha, luteolysis occurred, but doses of 5 or 10 mg of PGF2alpha were luteolytic in all mares. The 10-mg dose of PGF2alpha did not cause luteolysis in mares 1 day after ovulation, and caused luteolysis in only 2 of 5 mares on day 3 after ovulation. The same dose of PGF2alpha, however, caused luteolysis i...
McIntosh JE, Moor RM, Allen WR.The process involved in the disappearance of PMSG from the blood of sheep, following a single intravenous injection, has been separated into two exponential components. Values (mean plus or minus S.E.) calculated from experiments on five animals were: metabolic clearance rate (37.8 plus or minus 1.6 ml hr-minus 1); rate constant of disposal (0.0315 plus or minus 0.0016 hr-minus 1); half-time of disposal (21.2 plus or minus 1.1 hr). The stage of the oestrous cycle, ovariectomy and the dose of PMSG used had no apparent effect on these values.
Brand A, de Bois CH, Vandenhende R.Parenteral administration of 2.5-5 mg. of prostaglandin F2alpha to horses, 15 mg. to heifers or 25-30 mg to lactating cows and 15 mg. to sheep will induce regression of the corpus luteum (luteolysis) and a fertile oestrus within 48-72 hours. Because of their luteolytic effect prostaglandins may be used in various indications in the field of reproduction. An exception is the pig in which administration of prostaglandins does not induce luteolysis before D12 and therefore fails to induce oestrus. In horses, cattle and sheep, administration of prostaglandins during the first four days of the cycl...
Holtan DW, Nett TM, Estergreen VL.Jugular vein plasma from 13 mares was extracted with diethyl ether and chromatographed on Sephadex LH-20 columns (.5 × 9 cm) after which progesterone and 17α-hydroxyprogesterone (170HP) were quantified by a competitive protein binding radioassay. During pregnancy, progesterone increased (P < .05) from 1.1 ± .4 ng/ml (mean ± SE) on day 0 to 7.5 ± 1.2 ng/ml on day 8 followed by a transient (nonsignificant) decrease to 4.8 ± .4 ng/ml on day 28. From days 28 to 44 progesterone again increased (P < .05) attaining a maximum concentration of 15.2 ± 1.4 ng/ml on day 64. Thereafter progesterone ...
Engle CC, Foley CW.Uterine tubal fluids were collected twice a day from mares for 5 consecutive estrous cycles between March 15 and September 1. Follicular fluids were aspirated from the follicles of exteriorized ovaries of 3 mares between days 2 and 5 of estrus. Uterine tubal fluid and follicular fluid were analyzed for osmolarity, dry matter, total lipids, total free fatty acids, glucose, fructose, and lactic acid. Blood samples were collected (jugular venipuncture) throughout the estrous cycle, and the same physical and biochemical analyses were made on blood plasma. A difference (P less than 0.01) was found ...
Douglas RH, Ginther OJ.Nine groups of pony mares (3/group) were used in a 3 times 3 factorial experiment. The factors were dose of PGF-2 alpha (0, 0.25 of 1.25 mg and route of administration (im, iu or il). Mares were laparotomized and treated on day 7 postovulation. Jugular blood was collected for progesterone RIA at 0 (pretreatment) and 1,6,12,24,48, and 72 hr posttreatment. In mares given either 0.25 mg or 1.25 mg PGF-2alpha, progesterone concentrations were not significantly different among the three routes at any of the posttreatment times studied except at 6 hr posttreatment. In mares given 0.25 mg, progestero...
Watson ED.Corpora lutea were recovered from mares either 4 to 5 days or 12 to 13 days after ovulation. Mixed populations of luteal cells were prepared by collagenase digestion and were incubated for 24 h in the presence or absence of prostaglandin (PG) F-2 alpha (250 ng/ml). PGF-2 alpha significantly (P = 0.03) reduced progesterone secretion by cells from late diestrous corpora lutea and tended (P = 0.06) to reduce secretion by early diestrous cells. PGF-2 alpha had no significant effect on leukotriene B-4 (LTB-4) production by cells from early diestrous corpora lutea, but significantly (P = 0.03) incre...
Raz T, Carley S, Card C.The objective was to compare the effects of eFSH and deslorelin treatment regimes on ovarian stimulation and embryo production of donor mares in early spring transition. Starting January 30th, mares kept under ambient light were examined by transrectal ultrasonography. When a follicle > or =25 mm was detected, mares were assigned to one of two treatment groups, using a sequential alternating treatment design. In the eFSH group, mares (n=18) were treated twice daily with eFSH (12.5mg im) until they achieved a follicle > or =35 mm; hCG was given 36 h later. In the deslorelin group, mares (n=18) ...
Withrow JM, Sargent GF, Scheffrahn NS, Kesler DJ.Two pony mares were administered 150 mg of testosterone propionate every other day for 20 days (ten injections) and every ten days there-after. An additional two mares and one stallion were not treated and served as controls. Testosterone propionate was dissolved in absolute ethanol and administered subcutaneously. Sex behavior tests were conducted 26 and 40 days after the first injection. Control mares exhibited very little male sex behavior. Both testosterone propionatetreated mares, however, exhibited mounting, sniffing, flehmen, biting and vocalization behavior in the presence of an estrou...
Britton BA.Cervical and endometrial swabs were taken from 7 mares at various stages of the oestrous cycle. There was no consistent pattern of cell change throughout the cycle. The dominant cell in smears from normal mares was the columnar epithelial cell, especially in smears obtained during oestrus. A ciliated columnar epithelial cell was found much less frequently but appeared more often in smears before oestrus. Endometrial biopsies were also collected from 7 mares at intervals 2-3 weeks over an 8-month period from the beginning of spring to the end of autumn. There was no obvious change in the endome...
McCue PM, Troedsson MH, Liu IK, Stabenfeldt GH, Hughes JP, Lasley BL.Thirty-seven seasonally anoestrous mares were divided into treatment and control groups and given 10 micrograms of native GnRH (GnRH) per hour using a peristaltic pump, or 10 micrograms GnRH agonist (GnRHa) twice daily, beginning on either 13 January, 13 February or 14 March. Treatment with GnRH was equally effective in inducing ovulation in January (4/5), February (4/5) and March (3/4). GnRHa treatment was more effective in inducing ovulation in February (4/5) and March (4/4) than in January (2/8). Peak luteinizing hormone (LH) concentrations in mares induced to ovulate with GnRH (7.4 +/- 1.5...
Bhavnani BR, Woolever CA.A mixture of [4,8,12-14C]farnesyl pyrophosphate and [3H]dehydroepiandrosterone was injected into a horse fetus im during laparotomy, after which maternal urine was collected for 6 days. Steroid conjugates in the urine were extracted with Amberlite XAD-2 resin, hydrolyzed, and separated into phenolic and neutral fractions. Estrone, 17 alpha-estradiol, equilin [3-hydroxy-1,3,5(10),7-estratetraen-17-one], and 17 alpha-dihydroequilin [1,3,4(10),7-estratetraene-3,17 alpha-diol] were isolated from the phenolic fraction and their radiochemical purities were established. Only estrone and 17 alpha-estr...
Webel SK, Squires EL.The clinical effectiveness of the synthetic progestagen, altrenogest, was evaluated in field trials with 449 mares during the 1980 breeding season. An oral dose of 27 mg altrenogest was administered daily for 15 days. In the first trial treated mares were compared with controls, and in the second trial the effectiveness of treatment for prolonged or erratic spring oestrus was evaluated. Oestrus was suppressed in 94% of the treated mares in the first trial. The post-treatment response was related to the stage during the transition from winter anoestrus to the spring breeding season and degree o...
Fitzgerald BP.The purpose of this experiment was to investigate whether N-methyl-D,L-aspartate stimulated gonadotropin secretion in mares and to determine the response in two experimental paradigms where gonadotropin secretion is low or elevated. In Experiment 1, conducted during the breeding season (summer), eight long-term ovariectomized mares were treated daily for 21 d with progesterone plus estradiol (n = 4) or oil vehicle. Beginning on Day 14, each mare received, in a randomized design on alternate days, an intravenous injection of either 0, 0.5, 1.0, or 5.0 mg/kg NMA. Treatment with NMA was not accom...
Brand A, de Bois CH, Vandenhende R.Parenteral administration of 2.5-5 mg. of prostaglandin F2alpha to horses, 15 mg. to heifers or 25-30 mg to lactating cows and 15 mg. to sheep will induce regression of the corpus luteum (luteolysis) and a fertile oestrus within 48-72 hours. Because of their luteolytic effect prostaglandins may be used in various indications in the field of reproduction. An exception is the pig in which administration of prostaglandins does not induce luteolysis before D12 and therefore fails to induce oestrus. In horses, cattle and sheep, administration of prostaglandins during the first four days of the cycl...
Dehennin L, Petit E, Bonnaire Y, Bruyas JF, Le Bizec B, Plou P.Rules of horse racing stipulate that pregnant mares may compete under definite conditions of date, because early pregnant status may be misused for the sake of enhancing physical performance by putative anabolic steroid action. Screening for pregnancy is generally performed by plasma equine gonadotrophin (eCG) immunoassay, which covers the period between Days 40 and 120. In common screening for urinary anabolic steroids performed by gas chromatography-mass spectrometry, inclusion of two complementary criteria, i.e. the evaluation of total conjugates of 5(10)-estrene-3beta,17alpha-diol (EED) an...
Lowe JE, Foote RH, Baldwin BH, Hillman RB, Kallfelz FA.Three Quarter-horse mares were thyroidectomized at about 1.5 years of age. Three similar intact mares served as controls. The study continued through two breeding seasons. The thyroidectomized mares were lethargic, rear limbs were oedematous and hair coats were coarse. They displayed a tranquil oestrous behaviour when exposed to a stallion and were only mildly antagonistic when not in oestrus. Length of oestrous cycles varied but most often they were 19-24 days long. Duration of oestrus (mean +/- s.e.m.) for the control and thyroidectomized mares was 12.9 +/- 2.9 and 11.7 +/- 2.2 days respecti...
Briant C, Ottogalli M, Guillaume D.With the objective of controlling the day of ovulation, 40 mares were assigned to a control or three treated groups: A3d, A4d, and A5d. The treated groups received antarelix (Teverelix 0.01 mg/kg, i.v., twice a day) for 3, 4, or 5 days from the day the dominant follicle (F1) reached 28 mm (=D0), and one injection of hCG (1600 IU, i.v.) on D1, D2, or D3, respectively. Control mares received one injection of hCG when F1 reached 35 mm. Plasma LH, FSH, progesterone, and total estrogens were assayed. In the A3d, A4d, and A5d groups, 9 (90%), 6 (60%), and 5 (50%) out of 10 mares, respectively, ovula...
Magee C, Bruemmer JE, Nett TM, Squires EL, Clay CM.Kisspeptides (KiSS) are a recently discovered family of neuropeptides with a central role in regulating the onset of reproductive function in all animals studied to date. We have established biological and physiological evidence for KiSS signaling in the mare. The objective of the current study was to evaluate the physiological and behavioral responses of mares repeatedly given the equine-specific kisspeptpin decapeptide (eKp-10, YRWNSFGLRY-NH(2)) in an effort to shorten the interovulatory period. Administration of eKp-10 (0.5 mg iv every 4 h) to mares beginning on Day 16 postovulation (Group ...
Allen WE.The situations and conditions that can disrupt the mares normal oestrous cycle are described. Season of the year is a major influence; maximum reproductive efficiency does not totally coincide with the artificially defined "breeding season". Other abnormalities are associated with spontaneously persistent luteal function, psychological influences over behavioural activity, the presence of endometritis, multiple ovulation, reproductive behavior after pregnancy failure and granulosa cell tumours.
Mumford EL, Squires EL, Jasko DJ, Nett TM.A lack of pituitary LH stores has been implicated as the cause of seasonal anestrus and failure to ovulate during the spring transition period in mares. In this experiment, 40 mares were used to study the effects of GnRH, estrogen, and an estrogen-GnRH combination on increasing releasable pituitary LH. Mares were stratified based on their ability to secrete LH in response to a 950-micrograms challenge of GnRH (n = 10 per group) and then assigned to one of four treatment groups: 1) controls, given no treatment; 2) 1 mg of estradiol-17 beta in oil i.m. daily for 8 d; 3) 200 micrograms of GnRH an...
Martínez-Boví R, Cuervo-Arango J.The objectives were to determine: (i) whether intrafollicular administration of PGE2 and PGF2α to mares would hasten follicle collapse and (ii) the differences in reproductive hormone characteristics in mares with spontaneous and prostaglandin-induced follicle collapses. Six mares were followed for two oestrous cycles each: when the mares reached a follicle diameter of 30-35 mm and showed mild-to-moderate endometrial oedema, mares were administered a single 0.5 ml dose containing 500 μg PGE2 and 125 μg PGF2α (treatment cycle) or a placebo (0.5 ml of water for injection; control cycle) into...
Dippert KD, Hofferer S, Palmer E, Jasko DJ, Squires EL.Cyclic mares were assigned to 1 of 3 treatments (n=15 per group): Group 1 received equine pituitary extract (EPE; 25 mg, i.m.) on Day 5 after ovulation; Group 2 received EPE on Day 12 after ovulation; while Group 3 received 3.3 mg of GnRH analogue (buserelin implant) on the day of ovulation and 25 mg, i.m. EPE on Day 12. Mares in each group were given 10 mg PGF2alpha on the first and second day of EPE treatment. The EPE treatment was continued daily until the first spontaneous ovulation, at which time 3,300 IU of human chorionic gonadotropin (hCG) were given to induce further ovulations. Mares...
Larentis GR, Bastos HBA, Centeno LAM, Bueno VC, Bringel BA, Mattos RC.The present case report aimed to determine the responsiveness of the endometrium and the ovaries of an X0 mare after hormonal treatment. On transrectal palpation, the uterus was flaccid and smaller than normal, and the ovaries were small and smooth. The endometrium had normal histological architecture, with an atrophic glandular epithelium. A karyotype evaluation was performed, and 70 cells presented 63 chromosomes, lacking one sex chromosome. Circulating hormonal levels of total estrogens were 43.93 pg/mL; progesterone 0.01 ng/mL; testosterone 48 pg/mL; FSH 30.3 ng/mL; and LH 1.71 ng/mL. ...
Garcia MC, Ginther OJ.Six pony mares were ovariectomized (OVX) on day 16 of diestrus during June and July, 1972, to study short term changes in plasma luteinizing hormone (LH) concentrations. Plasma LH was higher (P less than .05) 3 days after OVX (1.76 ng/ml) than the day after OVX (1.01 ng/ml), and a gradual increase occurred over the first 2 weeks. Elevated plasma LH concentrations similar to mid-estrus levels were present from the 2nd to 11th week post-OVX. In another experiment, the same 6 OVX mares were bled once a month from February, 1973, to January, 1974, to study long-term changes in plasma LH in relatio...
Harrison LA, Squires EL, Nett TM, McKinnon AO.We hypothesized that the LH response to GnRH would be greater as the interval from foaling increases, whereas the FSH response would decrease, and that corpus luteum function after the first ovulation would be similar to that after the second ovulation. At parturition, mares were assigned to receive GnRH (2 micrograms/kg) intravenously on 1) d 3 postpartum (n = 6); 2) d 6 postpartum (n = 6); 3) d 1 of first postpartum estrus (foal estrus) and again on d 1 of second postpartum estrus (n = 8). Blood was collected through an indwelling cannula at -2, -1 and 0 h relative to GnRH stimulation (basal...
Bollwein H, Braun J.In this study the use of hCG for induction of ovulation is described. Factors such as follicle diameter at the time of administration of hCG (3000 IE hCG i.v.), follicular growth after hCG and the rate of double ovulations were evaluated. A total of 168 mares presented for artificial insemination were used. In 249 estrous periods hCG was given to mares exhibiting standing estrous when a minimum follicle diameter of 30 mm and a well developed edema of the endometrium could be detected by ultrasonography. In nine estrous periods ovulation occurred within 24 hours after hCG. The majority of mares...
Neely DP, Stabenfeldt GH, Kindahl H, Hughes JP, Kendrick JW.The intrauterine infusion of 500 ml of warm sterile saline solution into mares on days 12, 13, or 14 after ovulation failed to alter the ovulatory interval, although intervals were shorter for days 12 and 13 (20.6 days) when compared with those in control mares (21.6 days). The IU fusion shortened luteal-life-span on days 12 (12.0 vs 13.8 days) and 13 (13.0 vs 14.4 days) (P is less than 0.05), but not day 14 (14.0 vs 13.5 days), when comparing the effects of IU infusion with an average of before and after base-line data. There was no effect on the interval from corpus luteum regression to ovul...
Driancourt MA, Mariana JC, Palmer E.In the middle of the breeding season, 16 pony mares (n = 4 per day) were slaughtered on four different days (days 6, 14, 17 and the preovulatory day) of the oestrous cycle, day 0 being the day of the last ovulation. All the ovaries were examined histologically; the number, size and atresia (defined by granulosa cell pyknosis) of all follicles larger than 1 mm in diameter were studied, using a Kryotome-video recorder-TV system. Follicular distribution of all the sizes studied (1-5 mm, 5-10 mm, greater than 10 mm in diameter) was very similar in the right and left ovaries. However, compared to t...
Witt MC, Bollwein H, Probst J, Baackmann C, Squires EL, Sieme H.The aim of the present study was to investigate the effects of a gonadotropin treatment to induce superovulation on ovarian and uterine blood flow and its relationship with steroid hormone levels and ovarian response in mares, using color Doppler sonography. Each of six mares were examined sonographically in five cycles for 3 d (t1 to t3) during the follicular development phase (FDP) beginning at a follicle size of ≥ 22 mm, and for 4 d (D-4 to D-1; D0 = Ovulation) in the preovulatory phase (POP). After each examination, total estrogens (E(tot)) and progesterone (P(4)) levels were determined ...
Pantke P, Hyland J, Galloway DB, MacLean AA, Hoppen HO.Equine plasma luteinizing hormone (LH) possesses both biological (in vitro bioassay, B) and immunological (radioimmunoassay, I) activities and the ratio of B:I varies with stage of the oestrous cycle. To estimate the contribution made by pituitary secretion and peripheral metabolism to changes in the B:I ratio, pituitary venous effluent and circulating plasma from 5 dioestrous and 2 oestrous mares were analyzed using both an in vitro bioassay and a radioimmunoassay. During dioestrus, LH was released in a pulsatile fashion with a frequency of 1.4 pulses/24 h and a pulse duration of 20-40 min (c...
Tekin N, Yurdaydin N, Klug E, Yavas Y, Aksu A, Gülyüz F.Within a German-Turkish university partnership documentation of reproductive data of brood-mares was performed as a part project of the cooperation contract. In the study Arab, Haflinger and cross-breed mares were included. The mares mainly were housed in big studfarms and a smaller part was kept under small private farms. Almost three quarters of both the Arab and Haflinger mares exhibited an estrous length of 1-4 days, whereas the others showed a heat duration of a period of 5-10 days. In the same group of probands a mean length of sexual cycle of 18-24 days could be observed in 38.2% of the...
Ferreira-Dias G, Botelho M, Zagrajczuk A, Rebordão MR, Galvão AM, Bravo PP, Piotrowska-Tomala K, Szóstek AZ, Wiczkowski W, Piskula M, Fradinho MJ....Phytoestrogens exist in plants that are present in forages fed to horses. They may compete with 17-β estradiol and influence the estrous cycle. Therefore, the objective was to determine whether coumestrol from clover-mixed pastures is present in mare's plasma after their ingestion (experiment I), and when this phytoestrogen was present in mare's plasma after ingestion (experiment II). The effect of a long-term ingestion of phytoestrogens on estrous cycle disruption was assessed (experiment III; clinical case). Experiment I was carried out in nonpregnant anestrous and cyclic Lusitano mares (n ...
Solti L, Eulenberger K, Kurth D, Schöne L.Anoestrous mares were treated with prostaglandin (n = 43) and those that did not respond to prostaglandin (n = 29) with a synthetic progestagen, allyloestrenol, at a dose of 0.05 mg/kg body mass for 12 days. After the cessation of the long-term per os gestagen blockade the animals were checked for heat and, if a preovulatory follicle could be palpated, 2000 IU hCG was administered to induce ovulation. In some animals the plasma 17 beta-oestradiol (E2) and progesterone (P4) levels were also followed up throughout the gestagen treatment and for 10-14 days thereafter. As the favourable oestrus ra...
Bergfelt DR, Meira C, Fleury JJ, Fleury PD, Dell'Aqua JA, Adams GP.A regimen of progesterone plus estradiol (P&E) was used as a standard for ovarian synchronization to test the efficacy and evaluate the commercial application of ultrasound-guided follicle ablation as a non-steroidal alternative for ovulation synchronization in mares. Recipient mares at a private embryo transfer facility were at unknown stages of the estrous cycle at the start of the experiment on Day 1 when they were randomly assigned to an ablation group (n=18-21 mares) or to a P&E group (n=20-21 mares). In the ablation group, mares were lightly sedated and all follicles > or = 10...
Blue HB, Blue MG, Kenney RM, Merritt TL.Forty uterine fluid samples were obtained from 4 mares classified as resistant to uterine bacterial infection. The uterus of each mare was flushed with 50 ml of saline solution during estrus and diestrus of successive estrous cycles. Bacteria or fungi were isolated from 4 samples, and 7 additional samples were obtained from a mare with active intrauterine infection. Fluid volumes obtained during estrus (means = 40.3 +/- 11 ml) tended to be greater than those recovered during diestrus (means = 36.8 +/- 7.9 ml), but the difference was not significant. Concentrations and yields of protein in reco...
