The corpus luteum is a temporary endocrine structure in the ovaries of horses that forms after ovulation. It develops from the remnants of the ovarian follicle and is responsible for producing the hormone progesterone, which is essential for maintaining pregnancy. The formation, function, and regression of the corpus luteum are regulated by complex hormonal interactions, primarily involving luteinizing hormone (LH). Changes in the corpus luteum can influence reproductive cycles and fertility in mares. This page compiles peer-reviewed research studies and scholarly articles that explore the formation, function, and physiological significance of the corpus luteum in equine reproductive health.
Kelly CM, Hoyer PB, Wise ME.Dispersed horse luteal cells were used to evaluate the ability of horse LH, hCG and PMSG to stimulate progesterone secretion in vitro. Morphological characterization of these cells before gonadotrophin stimulation indicated the presence of two populations of cells based on cell diameters. In luteal cells incubated as suspended cells, horse LH and hCG stimulated (P less than or equal to 0.05) progesterone production at all levels of treatment. Stimulation of progesterone secretion by hCG was greater (P less than or equal to 0.05) than by horse LH over the range of concentrations utilized. When ...
Ginther OJ.One of the most profound theriogenology applications of transrectal diagnostic ultrasonography in mares involves the imaging of ovarian follicles and corpora lutea. The resolving capabilities (frequency) and quality of the scanner directly affect the minimal size of a structure that can be imaged and the quality of the image. High-frequency scanners (5 or 7.5 MHz) of good quality can image a 2-mm follicle and the corpus luteum throughout its functional life. A low-frequency scanner (3 or 3.5 MHz) can image a 6-mm follicle and the corpus luteum for several days after ovulation. Equine follicles...
Johnson AL, Becker SE, Roma ML.Standard bred mares that were cycling normally were treated beginning on Days 9 or 10 of the oestrous cycle with repeated pulses of GnRH (20 micrograms/h) and/or a single injection of prostaglandin (PG)F-2 alpha (alfaprostol, 3 mg), and were subsequently bled and palpated daily until the next ovulation. GnRH treatment increased serum concentrations of LH and progesterone at 4 days after the start of treatment compared to controls. The combination of PGF-2 alpha + GnRH treatment resulted in an immediate decline in serum progesterone values, and subsequently decreased the interval to next ovulat...
King SS, Evans JW.Follicular growth, circulating estradiol concentrations and endometrial prostaglandin F2 alpha (PGF2 alpha) production were measured to determine whether there is an interrelationship among these factors associated with luteolysis. Follicular growth was monitored by rectal palpation every other day during diestrus in 16 mares. Plasma estradiol was determined for daily samples during all estrous cycles. Endometrial tissue was removed for PGF2 alpha analysis by radioimmunoassay on d 10, 12, 14 or 16 during several normal cycles and after d 30 during spontaneously prolonged cycles. Circulating es...
Peyrot LM, Little TV, Lowe JE, Weber JA, Woods GL.Embryo autotransfer is defined as the collection of an embryo from and the transfer of this embryo into the same animal. The objectives of this study were to: 1) test the hypothesis that oviduct transport of the equine embryo from the oviduct into the uterus is not dependent on a unilateral embryo-corpus luteum interaction, 2) develop an embryo autotransfer technique for the mare and 3) compare the success rates of Day 4 embryos surgically autotransferred from the oviduct ipsilateral to ovulation to either the oviduct (n=10 mares) or the uterine horn (n=10 mares) contralateral to ovulation. Se...
Kastelic JP, Adams GP, Ginther OJ.Luteal progesterone was removed by an injection of prostaglandin F2alpha or bilateral ovariectomy on Day 12 of pregnancy in pony mares. The embryonic vesicle remained mobile in the uterus until loss occurred on Days 13, 13, 15, or 19 in four prostaglandin-treated mares and Days 15, 17, 19, or 26 in four ovariectomized mares. Exogenous progesterone given daily, starting on Day 12, maintained pregnancy until Day 40 in five of five prostaglandin-treated and three of four ovariectomized mares. During two-hour mobility trials on Day 14, embryonic vesicles in mares without luteal or exogenous proges...
Daels PF, Starr M, Kindahl H, Fredriksson G, Hughes JP, Stabenfeldt GH.The infusion of Salmonella typhimurium endotoxin into pregnant mares resulted in a biphasic release pattern of PGF-2 alpha as determined by 15-keto-13,14-dihydro-PGF-2 alpha concentrations. The initial phase of 1 h duration was followed by accentuated release by 2 h after infusion; concentrations reached basal levels by 6 h. In 7 mares at 23, 26, 29, 33, 36, 53 and 55 days of gestation, fetal death occurred between 36 and 120 h after infusion; 12 mares at 46, 51, 56, 59, 65, 71, 73, 85, 103, 138, 283 and 318 days of gestation did not abort after endotoxin infusion. Luteal activity was compromi...
Jeffcott LB, Hyland JH, MacLean AA, Dyke T, Robertson-Smith G.Pregnant Standardbred mares were allocated to 2 groups. On Day 45 of gestation, 20-45 ml saline (240 g NaCl/l) were injected into the fetal sacs of 10 mares, and the other 10 mares were given sham treatment. Post-operative plasma oestrone sulphate concentrations were lower (P less than 0.01) on Days 48-55 in saline-treated mares than in sham-treated mares. Mean plasma progesterone profiles were similar in the two groups of mares, although post-operative luteolysis occurred in 4 saline-treated mares. There was no difference in plasma CG profiles between the 2 groups, except that CG concentratio...
Johnson AL.Four seasonally anestrous mares (Standardbred), housed under a nonstimulatory photoperiod of 8 hours light:16 hours dark, were administered gonadotropin-releasing hormone (GnRH) in a pulsatile pattern (50 or 250 micrograms of GnRH/hour) for 8 to 18 days during February and March 1985. Treatment with GnRH, irrespective of dose or month, induced an increase in serum luteinizing hormone from a mean pretreatment value typical of anestrus (0.58 +/- 0.02 ng/ml +/- SE) to 10.84 +/- 1.27 ng/ml on day 8 of GnRH treatment. Ovulation in the 4 mares occurred 8.8 +/- 0.7 days after the initiation of pulsat...
Bazer FW, Vallet JL, Roberts RM, Sharp DC, Thatcher WW.Conceptuses produce steroids, prostaglandins, proteins and possibly other unidentified agents which may play a role in the establishment and maintenance of pregnancy. A key event in this process is protection of the corpus luteum (CL) from the luteolytic activity of prostaglandin (PG) F-2 alpha of uterine origin. Oestrogens produced by the pig conceptuses between Days 11 and 16 appear to exert an antiluteolytic effect resulting in the sequestering of PGF-2 alpha within the uterine lumen. Failure of the pregnant uterus to release PGF-2 alpha in an endocrine fashion, therefore, allows for mainte...
Lauderdale JW.Puberty: For the gilt and filly, the first corpus luteum (CL) appears to have a normal lifespan. For both species, first CL usually is associated with estrus but can form in the absence of estrus. For the ewe and cow, a transient (1 to 4 d, ewe; 3 to 10 d, cow) rise and fall of ovarian derived progesterone (P4) is detected in peripheral blood (80% of ewes; 50% of heifers) prior to first "normal" CL. The first CL of apparent normal lifespan is not accompanied by estrus in the ewe. The first CL in the cow may or may not be accompanied by estrus; first estrus in the cow can be anovulatory. Data a...
Thatcher WW, Bazer FW, Sharp DC, Roberts RM.Processes associated with "Maternal Recognition of Pregnancy" are reviewed extensively from the ovine, bovine, porcine and equine species. Comparisons among these species indicate that CL maintenance is achieved primarily by a predominant antiluteolytic-anti PGF effect, and there is strong evidence for antiluteolytic-luteoprotective and luteotropic controls that complement this basic system. The nature of the chemical signals (steroids, prostaglandins and proteins) to regulate these processes among the species are described. Common to all of the species reviewed is a change in vascular dynamic...
Malinowski K, Johnson AL, Scanes CG.The ability of interrupted photoperiods to induce early estrus and ovulation was examined. Horse mares were exposed to long (16 h light) or short (10 h light), noninterrupted photoperiods, ambient light, or various interrupted photoperiod treatments from December 1 to April 15 (135 d). Follicular development was assessed by rectal palpation and estrous behavior was determined by teasing with a stallion. Serum concentrations of progesterone were used as an indicator of corpus luteum function. Differences among the light treatment groups were compared for the following behavioral and ovarian cha...
Driancourt MA, Palmer E.An experiment was carried out on pony mares to establish the time of the oestrous cycle at which ovarian follicles are recruited for ovulation. In one group (n=7), the cycle was interrupted at the preovulatory stage by removing the preovulatory follicle; in another group (n=13) the cycle was interrupted at day 6 of the luteal phase by inducing luteolysis with a prostaglandin injection (PG). In a subgroup (n=7) of those given PG, the ovary not bearing the corpus luteum was removed at the time of injection. A further group (n=6) served as surgical controls. The interval to the next ovulation and...
Ginther OJ, Pierson RA.A linear-array ultrasound scanner with a 5-MHz transducer was evaluated for studying follicular and luteal status in mares, and the ultrasonic properties of equine ovaries were characterized. Follicular diameters were estimated in vivo and after removing and slicing six ovaries. Correlation coefficients between the two kinds of determinations were 0.91 for number of follicles >/=2 mm in diameter and 0.95 for diameter of largest follicle. The ovaries of five mares were examined daily until all mares had been examined from three days before an ovulation to three days after the next ovulation....
Zarrilli A, Lacalandra GM, Minoia P.In mare, sheep and bitch the action of PGF2 alpha have been studied in the early pregnancy. Prostin F2 alpha (Upjohn) and Gabbrostim (Vetem ) are commercial names of PGF2 alpha used at doses which are luteolytic in the non pregnant female. Seric progesterone showed a temporaneous decrease but after four or five days the initial values were restored and none of the experimental females aborted. In the opinion of authors, embryo per se and/or with its adnexa might have interacted blocking the mechanism of luteolysis induced by the administration of PGF2 alpha.
Roser JF, Evans JW.Changes in serum luteinizing hormone (LH) and progesterone concentrations, number of luteal unoccupied LH receptors, receptor affinity constants, luteal weights and luteal progesterone concentrations were determined during the postovulatory period in the mare. The number of unoccupied LH receptors and receptor affinity was less during the early (Days 1-4) and late [Day 15 through 3rd day after start of corpus luteum (CL) regression] luteal phases than during the mid-luteal (Days 9-14) phase of the postovulatory period (P less than 0.01). The number of LH receptors per CL increased 21-fold (P l...
Mattioli M, Galeati G, Seren E.Prostaglandin F-2 alpha (PGF-2 alpha) receptors of bovine and equine corpora lutea (C.L.) were studied. From both the equilibrium binding data and the dissociation kinetics behaviour, two affinity classes of receptors are evident in the mare, with apparent dissociation constants (Kd) of 1,5 x 10(-9) M and 3.5 x 10(-8) M. Bovine PGF-2 alpha receptors present a homogeneous population of binding sites with Kd = 1 x 10(-8) M. Both bovine and equine C.L. receptors bind PGF-2 alpha in a specific manner; only 13, 14-dihydro-PGF-2 alpha considerably cross-reacts with these receptors. Since in the mare...
Howey WP, Jochle W, Barnes WJ.Alfaprostal (K 11941), a novel prostaglandin F2 alpha analogue was clinically tested in 24 dioestrous mares, 40 anoestrous mares and 31 postpartum mares, all being given 2 or 3 mg intramuscularly. Blood samples were taken for the determination of plasma progesterone levels and the objective confirmation of luteolytic drug effects. Two hundred and thirty-six mares at the same location were used for comparisons of the rates of pregnancy, early embryonic loss and foaling. Alfaprostol was found to act as a potent luteolytic agent with good oestrus induction, follicular development and normal conce...
Saltiel A, Calderon A, Garcia N, Hurley DP.Ovarian activity, as measured by the presence of small (10-15 mm diam.), medium (15-30 mm) and large (greater than 30 mm) follicles, corpora haemorrhagica and corpora lutea (CL), was determined in a total of 3584 ovaries during 1 year using post-mortem specimens. There were significant correlations of the incidence of ovulated follicles (ovulations), large and medium follicles (P less than 0 . 001) and of the mean number of small follicles (P less than 0 . 05) per mare with respect to season. The yearly averages of ovulated, large and medium follicles were 30 . 1, 13 . 9 and 73 . 9%, respectiv...
Urwin VE, Allen WR.Concentrations of FSH, LH, chorionic gonadotrophin (CG) and progesterone were measured during early pregnancy in mares and donkeys carrying normal intraspecies and transferred extraspecies conceptuses. A secondary rise in progesterone concentrations occurred in normal intraspecies horse and donkey pregnancy soon after the appearance of CG but FSH concentrations continued to fluctuate and were not influenced by CG production. In donkeys carrying transferred horse conceptuses FSH concentrations fell sharply and progesterone concentrations rose steeply, coincidental with the appearance of abnorma...
Roser JF, Evans JW, Mikuckis GM, Adams TE, Hughes JP.As quantified by Scatchard analysis, a 27 000 g crude luteal membrane fraction contained a single population of unoccupied LH receptors characterized by high affinity, ka = 0.647 +/- 0.158 X 10(11) M-1 and low binding capacity, Rt = 4.91 +/- 0.78 X 10(-11) M/mg membrane fraction. Acceptable hormonal specificity, reversibility, saturability, high affinity and tissue specificity indicated that the binding protein was a physiological receptor. To ensure that the methods used for Scatchard analysis were valid, hCG was characterized for specific activity and maximum bindability, non-specific bindin...
Baker CB, Newton DI, Mather EC, Oxender WD.The length of diestrus was not changed in 4 mares by taking endometrial biopsy specimens during estrus. In contrast, taking endometrial biopsy specimens on postovulation day 4 induced premature luteolysis and significantly (P less than 0.05) reduced the length of diestrus. A concurrent decrease in serum progesterone occurred to verify the premature luteolysis in these mares. Bacterial cultures of endometrial swab samples from these mares were negative for growth at the first estrus before and after the last biopsy procedures, indicating that luteolysis was induced by the biopsy procedure and w...
van Niekerk CH, Morgenthal JC, Gerneke WH.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 ...
Woodley SL, Burns PJ, Douglas RH, Oxender WD.This study was designed to test if oestradiol treatment would prevent or delay luteolysis in mares. Mares (5/group) received 0, 0.1, 1.0 or 10.0 mg oestradiol-17 beta daily from the day of ovulation until the next ovulation or for a maximum of 32 days. This treatment did not prevent luteolysis which occurred 15.8, 16.8, 15.8 and 17.3 days after the previous ovulation for the mares treated with 0, 0.1, 1.0 and 10.0 mg oestradiol respectively. Although oestradiol treatment failed to alter oestrous behaviour after luteolysis, daily treatment with 10.0 mg oestradiol prevented follicular growth and...
Condon WA, Ganjam VK, Kenney RM.Corpora lutea (CL) from 7 mares were sliced and incubated for 2 h with ovine LH and various sympathomimetic agonists and blockers. None of these compounds was able to cause a significant increase in either progesterone or total progestagens by the luteal tissue. This is in contrast to earlier studies with bovine luteal tissue, and indicates that the equine CL is more refractory to exogenous stimulation than in the bovine CL.
Ginther OJ.Recent findings on the luteolytic process in mares are reviewed and differences from other farm species are noted. It is well known that the luteolysin, PGF2α (PGF), is secreted from the endometrium in the absence of pregnancy in farm animal species. But PGF is a potent chemical and safeguards have evolved so that only the corpus luteum (CL) is affected. The safeguards include a short PGF half-life and secretion in two or three pulses per day. In mares, endogenous PGF travels from the uterus to the CL through the systemic circulation, but the luteal-cell membranes are highly efficient in capt...
Vernon MW, Strauss S, Simonelli M, Zavy MT, Sharp DC.The binding of prostaglandin (PG) F-2 alpha to corpora lutea (CL) from pregnant and non-pregnant Pony mares was examined. Studies of the rates of association and dissociation indicated that [3H]PGF was bound specifically and reversibly to a luteal cell membrane preparation (MP) that was isolated by high speed (100,000 g) ultracentrifugation. Various PGs and PG metabolites displaced [3H]PGF from the receptors in the following decreasing order: PGF-2 alpha greater than 13, 14-dihydro-PGF-2 alpha = 13,14-dihydro-15-keto PGF-2 alpha greater than PGD-2 greater than PGF-1 alpha = PGE-2 greater than ...
Baker CB, Newton DI, Mather EC, Oxender WD.The length of diestrus was not changed in 4 mares by taking endometrial biopsy specimens during estrus. In contrast, taking endometrial biopsy specimens on postovulation day 4 induced premature luteolysis and significantly (P less than 0.05) reduced the length of diestrus. A concurrent decrease in serum progesterone occurred to verify the premature luteolysis in these mares. Bacterial cultures of endometrial swab samples from these mares were negative for growth at the first estrus before and after the last biopsy procedures, indicating that luteolysis was induced by the biopsy procedure and w...
Rodger FE, Illingworth PJ, Watson ED.Although the mare corpus luteum (CL) is capable of aromatization, the expression of other enzymes involved in estradiol synthesis is not yet clear. This study examined the localization of P450C17 in the mare CL at different stages of its functional development. In ovaries from follicular phase mares P450C17 was localized in the theca cells of ovarian follicles. Following ovulation, no immunostaining for P450C17 was detected in the mature CLs of nonpregnant mares. In pregnant mares, no immunostaining for P450C17 was identified in the corpus luteum prior to secretion of eCG by the feto placental...
Montavon S.Because of the anatomical position of the Corpus luteum within the ovary, rectal palpation is of little value for identification and evaluation. The aim of this review is to familiarize the practitioner with the echographic examination of the Cl. He should be able to recognize different stages of this important structure and to correlate ovulation and the existence of the Cl. Various specific criteria and details regarding equine echography are reported and illustrated, using the the most recently published scientific data.
King SS, Evans JW.Follicular growth, circulating estradiol concentrations and endometrial prostaglandin F2 alpha (PGF2 alpha) production were measured to determine whether there is an interrelationship among these factors associated with luteolysis. Follicular growth was monitored by rectal palpation every other day during diestrus in 16 mares. Plasma estradiol was determined for daily samples during all estrous cycles. Endometrial tissue was removed for PGF2 alpha analysis by radioimmunoassay on d 10, 12, 14 or 16 during several normal cycles and after d 30 during spontaneously prolonged cycles. Circulating es...
Ginther OJ, Wolf CA, Baldrighi JM, Greene JM.Hourly circulating concentrations of a PGF2α metabolite (PGFM), progesterone (P4), and LH were obtained from a reported project, and concentrations of nitric oxide (NO) metabolites (NOMs; nitrates and nitrites) were determined in eight mares. Unlike the reported project, hormone concentrations were normalized to the peak of the first PGFM pulse of luteolysis (early luteolysis), second PGFM pulse (late luteolysis), and a pulse after luteolysis. The duration of luteolysis was 23.1 ± 1.0 hours, and the peak of the first and second PGFM pulses occurred 6.5 ± 0.9 and 14.8 ± 0.8 hours after the ...
Hohenhaus MU, Lehmann B.Ultrasonography is a good means of monitoring follicular development in the mare and allows objective observation and measurement of follicular growth as well as identification of corpora lutea and hematoma in the ovary. The significance of ultrasonography in this field lies in the specific anatomical structure of the mare's ovary and the different phenomena preceding and accompanying ovulation, which are described in this paper. The last part deals with the handling and use of ultrasonography.
Zarrilli A, Lacalandra GM, Minoia P.In mare, sheep and bitch the action of PGF2 alpha have been studied in the early pregnancy. Prostin F2 alpha (Upjohn) and Gabbrostim (Vetem ) are commercial names of PGF2 alpha used at doses which are luteolytic in the non pregnant female. Seric progesterone showed a temporaneous decrease but after four or five days the initial values were restored and none of the experimental females aborted. In the opinion of authors, embryo per se and/or with its adnexa might have interacted blocking the mechanism of luteolysis induced by the administration of PGF2 alpha.