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Topic:Gonadotropins
Gonadotropins are hormones that play a significant role in the reproductive physiology of horses. They are primarily produced by the pituitary gland and include luteinizing hormone (LH) and follicle-stimulating hormone (FSH). These hormones regulate various aspects of equine reproduction, such as the development and function of the ovaries in mares and the testes in stallions. Gonadotropins influence processes like follicular growth, ovulation, and spermatogenesis. Their levels and activity are subject to regulation by factors such as seasonality and age, affecting reproductive efficiency in horses. This page compiles peer-reviewed research studies and scholarly articles that explore the function, regulation, and implications of gonadotropins in equine reproductive health.
[Endometrial cups in horses]. Endometrial cups in horses are outgrowths appearing in the uterine wall of the pregnant horn between approximately 38 days and 150 of gestation. The cups are structures which vary in shape from oval to irregular and have distinct raised edges, showing an ulcer-like form. The maximum measurements are approximately 5 X 2.5 X 2.5 cm. Microscopic examination shows that they consist of large epithelioid decidual-like cells having large nucleoli. Pregnant Mare Endometrium Gonadotrophin (PMEG) is produced in the endometrial cups. PMEG may be regarded as a precursor of Pregnant Mare Serum Gonadotrophi...
Passive immunization of cyclic mares against androgen: gonadotropin and progesterone concentrations and estrous characteristics. Antiserum generated in a horse against testosterone conjugated to bovine serum albumin (BSA) was administered to six lighthorse mares (androgen-immunized mares) 1 to 3 d before a prostaglandin-induced estrus and twice again at 2-d intervals. Six control mares were administered antiserum generated against BSA on the same schedule. Relative to testosterone, cross-reactivities of other steroids with the testosterone antiserum were (%): dihydrotestosterone, 52; 5 alpha-androstane-3 alpha,17 beta-diol, 8.6; androst-4-ene-3,17-dione, 1.2; and all others tested less than .1. Tritiated testosterone bi...
Circadian, circhoral and seasonal variation in patterns of gonadotrophin secretion in geldings. Blood samples were obtained from 5 mixed-breed, long-term castrated geldings during five 24-h periods between May 1984 and April 1985. Blood samples were collected, beginning at 09:00 h, at 15-min intervals for 8 h and hourly for the remaining 16 h. Plasma concentrations of LH and FSH were determined by RIA. Seasonal changes in hormone concentrations and frequency and amplitude of secretory pulses were evaluated. No diurnal variation in either LH or FSH secretion was observed: however, marked circhoral fluctuations in LH and FSH secretion were noted. Mean LH and FSH concentrations in these lon...
Alternative solutions to hCG induction of ovulation in the mare. Injection of hCG (2000-2500 i.u., i.v.) to mares when a follicle reaches 35 mm induces ovulation between 24 and 48 h. However, repeated injections induce antibodies against hCG. We report attempts to induce ovulation without this inconvenience. We called 'response' an ovulation between 24 and 48 h after treatment. The typical response to hCG was obtained in 73% (N = 145) of treated mares. After immunization against hCG, the response (0%, N = 10) was less than in nonimmunized controls (100%, N = 9). Simultaneous injection of dexamethasone and hCG resulted in induction of ovulation (71%, N = 14)...
Application of recombinant DNA techniques to structure-function studies of equine protein hormones. Complementary (c)DNA libraries have been made from horse pituitary gland and endometrial cup tissues with the aim of isolating the genes for the horse gonadotrophins (FSH, LH and CG) and growth hormone (GH). Southern (DNA) and Northern (RNA) blotting techniques were used to demonstrate that several heterologous (human and ovine) cDNA probes would be adequate for isolating the horse genes. A human cDNA probe was then used to isolate the horse gonadotrophin alpha-subunit cDNA from the pituitary and endometrial cup libraries. The nucleotide sequences from both tissue sources were identical, there...
Secretion of luteinizing hormone and follicle stimulating hormone in intact and ovariectomized mares in summer and winter. Sequential samples of blood were drawn via jugular catheters every 15 min for 24 h from four mares in each of five reproductive states: intact anestrous mares in winter, intact diestrous mares in summer, intact estrous mares in summer, ovariectomized mares in winter and ovariectomized mares in summer. Estrous mares were sampled on d 4 or 5 of estrus and diestrous mares on d 10 or 11 of diestrus. Each sample of plasma was assessed for concentrations of luteinizing hormone (LH) and follicle stimulating hormone (FSH) in two independent radioimmunoassays. A computer program was developed that dete...
Changes in thecal and granulosa cell LH and FSH receptor content associated with follicular fluid and peripheral plasma gonadotrophin and steroid hormone concentrations in preovulatory follicles of mares. Individual antral follicles from 11 horse mares were studied at three stages of the oestrous cycle to determine the characteristics of the presumptive ovulatory follicle. Mares were ovariectomized (ovex) during the late luteal phase on Day 14 after ovulation (Group 1) and on the 1st (Group 2) or 4th (Group 3) day of oestrus. Every follicle greater than 5 mm in diameter was dissected from each ovary; follicles greater than or equal to 15 mm in diameter were analysed separately while others were pooled by size for subsequent analyses. The presumptive ovulatory follicle possessed the following ch...
Effect of pulsatile gonadotrophin release on mean serum LH and FSH in peri-parturient mares. Changes in the pattern of LH and FSH in serum were studied in 6 mares foaling during the summer. Samples were collected frequently (every 15 min) for 24 h twice before foaling, -33 +/- 2 and -12 +/- 2 days, and for 12 h after foaling, on Day 0 and Day 4. Simultaneous pulses of FSH and LH were observed before foaling (r2 = 0.99). Before foaling, gonadotrophin pulses were infrequent (6 in 264 h of observation). On the day of foaling, LH and FSH pulse frequency increased (P less than 0.005) with 2-4 pulses per mare. The amplitudes of pulses of LH and FSH were higher before parturition than for th...
Comparison of two reference preparations for horse chorionic gonadotrophin in four in-vivo and in-vitro assays. A number of horse chorionic gonadotrophin (CG) preparations of different purities and from diverse sources have been compared in radioimmuno-, radioreceptor, in-vitro cell culture, and in-vivo assays. The relative activities of the great majority of the preparations tested were consistent in the 4 assay systems. Moreover, their relative activities in the 4 assays were consistent with those found for unfractionated plasmas. These preparations were therefore considered to represent the native form of hormone. The second International Reference Preparation (IRP2) was among the few preparations ex...
Comparison of equine pituitary extract and follicle stimulating hormone for superovulating mares. Sixty light-horse, nonlactating mares were used to compare the efficacy of equine pituitary extract versus follicle stimulating hormone (FSH-P) for inducing multiple ovulations. On Day 12 of diestrus, mares were assigned to receive 1) no treatment, controls; 2) subcutaneous injections of 750 Fevold rat units of equine pituitary extract once daily; or 3) intramuscular injection of 150 mg of FSH-P twice daily. Ultrasound was used twice daily to visualize follicular changes and ovulation. For mares in Groups 2 and 3, treatment was initiated when two or more follicles > 20 mm were detected, and...
Androgen and estradiol effects on gonadotropin secretion and response to GnRH in ovariectomized pony mares. In Exp. 1, 16 long-term ovariectomized pony mares were used to determine the effects of treatment with estradiol benzoate (EB) and dihydrotestosterone (DHT) benzoate alone, and in combination, on secretion of follicle stimulating hormone (FSH) and luteinizing hormone (LH) in daily blood samples and after three consecutive injections of gonadotropin releasing hormone (GnRH). Administration of EB alone, or in combination with DHT, every other day for 11 d reduced (P less than .05) concentrations of FSH and increased (P less than .05) concentrations of LH in daily blood samples, and increased (P ...
Direct demonstration of intrinsic follicle-stimulating hormone receptor-binding activity in acid-treated equine luteinizing hormone. After dissociating equine gonadotropins as a function of time at pH 3, we examined them by radioligand assay and sodium dodecyl sulfate polyacrylamide gel electrophoresis under nondissociating conditions (low, 0.1% SDS). Equine follicle-stimulating hormone (FSH) rapidly lost its receptor-binding activity, and low SDS-polyacrylamide gels demonstrated dissociation into subunits. Maximum dissociation occurred after 20-30 min of pH 3 incubation. Equine luteinizing hormone (LH), however, retained most biologic activity and was largely intact after 72 h of pH 3 incubation. Dose-response curves of ac...
Demonstration of a COOH-terminal extension on equine lutropin by means of a common acid-labile bond in equine lutropin and equine chorionic gonadotropin. The beta subunits of equine lutropin and equine chorionic gonadotropin were incubated in 0.013 N HCl for 30 min at 110 degrees C and separated into two fragments by reverse-phase high performance liquid chromatography. The amino acid and carbohydrate compositions of both fragments from each subunit were analyzed. The results demonstrated that equine lutropin-beta has a glycosylated COOH-terminal extension that differs only in carbohydrate composition from the COOH-terminal portion of equine chorionic gonadotropin-beta. This is the first demonstration of a glycosylated COOH-terminal extension i...
Effects of dihydrotestosterone benzoate administration on gonadotropin secretion in ovariectomized pony mares. Eight long-term ovariectomized pony mares were treated with either dihydrotestosterone (DHT) benzoate (400 micrograms/kg body weight) in safflower oil or an equivalent amount of oil every other day for 21 d to determine the effects of DHT on follicle stimulating hormone (FSH) and luteinizing hormone (LH) concentrations in blood samples drawn once daily and after administration of three successive injections of gonadotropin releasing hormone (GnRH). The GnRH injections were given at 4-h intervals on the day following the last DHT or oil injection. Treatment with DHT benzoate did not alter (P gr...
Delayed follicular development and ovulation following inhibition of FSH with equine follicular fluid in the mare. In two experiments, PGF(2alpha) was given to all mares on Day 10 (ovulation = Day 0). In experiment 1, mares received either whole follicular fluid or saline i.v. every 12 hours on Days 10 to 14. Experiment 2 was similar to experiment 1, except the follicular fluid was extracted with charcoal to remove steroids. Analysis of the FSH data for Days 10 to 21 indicated an effect of treatment (P<0.08) with whole follicular fluid, but not with charcoal-extracted follicular fluid. However, there was an effect of day (P<0.05) and an interaction (P<0.01) of treatment with day for both experimen...
Patterns of secretion of luteinizing hormone, follicle stimulating hormone and testosterone in stallions during the summer and winter. Samples of jugular blood were drawn from each of five stallions every 15 min for 12 h during the summer and winter to determine the short-term fluctuations in plasma concentrations of luteinizing hormone (LH), follicle stimulating hormone (FSH) and testosterone. Concentrations of LH and FSH were generally not pulsatile, although one stallion exhibited three distinct pulses in these hormones during the winter. In general, patterns of secretion of all three hormones were similar in both seasons and the number of significant rises in hormonal concentrations did not differ between seasons. Concent...
Physiological peripubertal activation of the ovary is not reproduced by pregnant mare serum gonadotropin (PMSG) administration. During the days preceding the first ovulation the ovary of the rat exhibits a remarkable increase in estradiol (E2) and progesterone (P) release in response to gonadotropins. No such increase is observed in the case of androgens (A, testosterone + dihydrotestosterone). The present experiments were undertaken to examine the possibility of reproducing these developmental events by stimulating the ovary with a gonadotropin that has substantial FSH-like activity. In vivo administration of pregnant mare serum gonadotropin (PMSG) to juvenile 29-day-old rats greatly increased the in vitro E2 and A re...
Chemical, biological and immunological properties of pituitary gonadotropins from the donkey (Equus asinus): comparison with the horse (Equus caballus). Donkey gonadotropins (donkey luteinizing hormone, dLH; donkey follicle-stimulating hormone, dFSH) have been isolated in purified form from 191 donkey pituitaries using essentially the same procedures previously employed for the purification of equine gonadotropins. Chemically, dLH and dFSH were observed to be similar to equine LH (eLH) and FSH (eFSH) in fractionation behavior and glycoprotein nature. Two forms of the dFSH molecule were observed, as is the case for eFSH. Donkey LH had significantly less total carbohydrate (13.5%) and sialic acid (1.9%) than eLH (26.7% and 5.8%, respectively). C...
Testosterone effects on gonadotropin response to GNRH: cows and pony mares. Effects of testosterone propionate (TP) treatment on plasma concentrations of luteinizing hormone (LH) and follicle-stimulating hormone (FSH) before and after an injection of gonadotropin releasing hormone (GnRH) were studied using ovariectomized cows and pony mares. An initial injection of GnRH (1 microgram/kg of body weight) was followed by either TP treatment or control injections for 10 (cows) or 11 (ponies) d. A second GnRH injection was administered 1 d after the last TP or oil injection. Concentrations of LH and FSH were determined in samples of plasma taken before and after each GnRH i...
Effects of placement of intravaginal sponges on LH, FSH, estrus and ovarian activity in mares during the nonbreeding season. Eight seasonally anestrous mares were administered intravaginal polyurethane sponges on December 15 and then weekly thereafter until February 1. Control mares received no sponges or genital contact. Sponge insertion caused an immediate surge in follicle-stimulating hormone (FSH) concentrations in jugular plasma in 50% of treated mares whereas no control mares had surges in FSH (P less than .05). The effect of treatment on luteinizing hormone (LH) concentrations was much less dramatic and only three treated mares appeared to have positive responses. Sponge-treated mares exhibited positive respo...
[Origin of the FSH + LH double activity of equine chorionic gonadotropin (eCG/PMSG)]. The LH and FSH activities of equine choriogonadotropin (eCG) have been compared in several species with those of the highly purified homologous pituitary gonadotropins. The molar FSH/LH activity ratio of eCG determined by RRA is 0.20 in the pig, 0.25 in the rat and 0 in the horse. These data demonstrate the LH monospecificity of eCG in its own species as it is the case for hCG. We have also shown that equine LH exhibited a FSH-activity similar to that of eCG in the pig and in the rat but not in the horse. In the female rat, the binding activity to FSH receptors and the in vitro FSH activity of...
The use of heterologous radioimmunoassays for the measurement of follicle-stimulating hormone and luteinizing hormone concentrations in horse and donkey serum. Heterologous double-antibody radioimmunoassay were developed for the measurement of FSH and LH concentrations in the serum of both horses and donkeys. The FSH assay employed a rabbit anti-ovine FSH serum which showed a complete lack of cross-reaction with equine chorionic gonadotrophin (eCG) and negligible cross-reaction with equine LH. The LH assay utilized an antiserum raised against highly purified eCG. This similarly showed negligible cross-reaction with equine FSH but its high cross-reactivity with eCG prevented the measurement of equine LH concentrations in serum when eCG was also presen...
Follicle stimulating hormone, luteinising hormone and progesterone concentrations in the blood of thoroughbred mares exhibiting single and twin ovulations. The concentrations of follicle stimulating hormone, luteinising hormone and progesterone were measured in serial blood samples taken throughout one or more oestrous cycles from 12 Thoroughbred mares, some of which exhibited single and others twin ovulations. The resulting profiles clearly demonstrated that no simple relationship exists between circulating gonadotrophin levels and subsequent ovulation rate in the mare. However, plasma progesterone concentrations during dioestrus are, as expected, higher following twin than single ovulations. The findings suggest that the underlying cause of twi...
Release of 3H2O from 1 beta,2 beta[3H]androstenedione by equine granulosa cells. Granulosa cells were harvested from mares at various stages of the oestrous cycle and incubated in Krebs-Ringer bicarbonate buffer with 1 beta,2 beta[3H]androstenedione as substrate. The release of 3H2O expressed as CPM/h/mg protein varied from 44000 to 768000 in follicles from 7 mares. The release of 3H2O was not significantly altered by luteinizing hormone, follicle stimulating hormone or pregnant mare's serum gonadotrophin. There was a significant negative correlation between the release of 3H2O and the concentration of progesterone in the follicular fluid. Based on the assumption that the ...
Induction of multiple ovulations during the ovulatory season in mares. The efficacy of an equine pituitary extract for induction of multiple ovulations during the ovulatory season was studied in 112 horse mares in four experiments. Combined for all experiments, 70% of the mares (78/112) had multiple ovulations for an average of 3.0 ovulations per mare. The interval between first and last ovulation was decreased (P<0.01) when human chorionic gonadotropin (hCG) was included in the treatment regimen (0.0+/-0.0 versus 1.6+/-0.4 days). Ovulation rate was lower (P<0.01) when extract treatment was initiated at day 19 (1.3+/-0.2) than when initiated at day 15 post-...
Testosterone administration to mares during estrus: duration of estrus and diestrus and concentrations of LH and FSH in plasma. To study the possible role of ovarian androgens in regulation of follicle stimulating hormone (FSH) secretion in the cycling mare, five mature, intact mares were treated with testosterone (20 micrograms/kg of body weight) daily during estrus; five control mares received safflower oil on the same schedule. Mares were teased for estrus and samples of jugular blood were drawn daily through one full estrous cycle. Concentrations of FSH in plasma were measured by a newly developed radioimmunoassay based on anti-ovine FSH serum and radioiodinated equine FSH. Testosterone treatment during estrus had ...
Effects of melatonin and thyrotropin releasing hormone on mares during the nonbreeding season. Two hormonal treatments, chosen for their effectiveness in other seasonally breeding species, were tested in mares during the nonbreeding season to determine if they could induce ovarian activity and estrus during the winter. Of 15 functionally anestrous (anovulatory) mares, five received intravaginal, polyurethane sponges containing .75 g of melatonin on December 16; fresh sponges containing melatonin were inserted weekly until February 3. These mares also received daily injections of saline. Five other mares received daily im injections of 100 micrograms of thyrotropin-releasing hormone (TRH...
Effects of injected ovarian steroids on reproductive patterns and performance in post-partum mares. Treatment of foaling mares with 150 mg progesterone and 10 mg oestradiol daily beginning within 12 h of parturition resulted in a delay of ovulation (15.6 +/- 2.6 days compared with 10.3 +/- 2.4 days in untreated mares). When mares were mated after this 5.3-day delay there was no advantage in reproductive performance over that of mares mated according to a conventional management system. Gonadotrophin secretion was inhibited during treatment but the following secretory patterns were similar to those of normal oestrous periods.
Equine follicle-stimulating hormone. Purification, acid dissociation, and binding to equine testicular tissue. A simple method of purification of equine follicle-stimulating hormone is described by which two forms of the hormone are obtained. The acid dissociation of the most active preparation was studied and a pKa of 5.8 was determined at 37 degrees C. This value is 2 pH units higher than that observed for pregnant mare serum gonadotropin suggesting that the binding areas between subunits are not identical in the two hormones. We also describe an homologous radioreceptor assay of equine follicle-stimulating hormone which is highly specific for this hormone in contrast to the heterologous systems desc...
Behavioral, follicular and gonadotropin changes during the estrous cycle in donkeys. Sexual behavior, follicular development and ovulation, and concentrations of circulating gonadotropins during the estrous cycle were studied during the summer in 7 jennies. Mean behavioral estrous length was 6.4 +/- 0.6 days (mean +/- SEM, n=19; 5.6 +/- 0.5 days preovulatory and 0.8 +/- 0.2 days post-ovulatory). Mean diestrous length was 19.3 +/- 0.6 days (n=14). Females in estrus typically showed posturing, mouth clapping, clitoral winking, urinating and tail raising. Mouth clapping began approximately one day sooner and lasted approximately one day longer than winking and tail raising, so th...
