Analyze Diet

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.
In vivo effect of epidermal growth factor, interleukin-1beta, and interleukin-1RA on equine preovulatory follicles.
Biology of reproduction    December 11, 2002   Volume 68, Issue 5 1748-1754 doi: 10.1095/biolreprod.102.012138
Martoriati A, Duchamp G, Gérard N.Paracrine factors have significant effects during folliculogenesis. Because of various morphological features, the mare is a convenient model to study in vivo the effects of factors involved in periovulatory events. In the present work, epidermal growth factor (EGF; experiment 1, n = 49 mares) and interleukin-1beta and interleukin-1RA (IL-1beta and IL-1RA, respectively; experiment 2, n = 80 mares) were injected intrafollicularly to evaluate the influence of these factors on in vivo maturation of equine preovulatory follicles. A transvaginal ultrasound-guided injection was performed when the di...
The relationship between body condition, leptin, and reproductive and hormonal characteristics of mares during the seasonal anovulatory period.
Journal of animal science    November 5, 2002   Volume 80, Issue 10 2695-2703 doi: 10.2527/2002.80102695x
Gentry LR, Thompson DL, Gentry GT, Davis KA, Godke RA, Cartmill JA.An experiment was conducted to determine the effects of high vs low body condition scores (BCS) produced by restricted feeding on reproductive characteristics, hormonal secretion, and leptin concentrations in mares during the autumnal transition and winter anovulatory period. Mares with BCS of 6.5 to 8.0 were maintained on pasture and/or grass hay, and starting in September, were full fed or restricted to produce BCS of 7.5 to 8.5 (high) or 3.0 to 3.5 (low) by December. All but one mare with high BCS continued to ovulate or have follicular activity during the winter, whereas mares with low BCS...
Pituitary responsiveness to GnRH in mares following deslorelin acetate implantation to hasten ovulation.
Journal of animal science    November 5, 2002   Volume 80, Issue 10 2681-2687 doi: 10.2527/2002.80102681x
Johnson CA, Thompson DL, Cartmill JA.The present experiment characterized the pituitary responsiveness to exogenous GnRH in the first 10 d after ovulation following commercially available deslorelin acetate implantation at the normal dosage for hastening ovulation in mares. Twelve mature, cyclic mares were assessed daily for estrus and three times weekly for ovarian activity starting May 1. Mares achieving a follicle at least 25 mm in diameter or showing signs of estrus were checked daily thereafter for ovarian characteristics. When a follicle >30 mm was detected, mares were administered either a single deslorelin acetate impl...
Comparison of the effects of two GnRH antagonists on LH and FSH secretion, follicular growth and ovulation in the mare.
Reproduction, nutrition, development    October 31, 2002   Volume 42, Issue 3 251-264 doi: 10.1051/rnd:2002023
Guillaume D, Bruneau B, Briant C.The effects of two GnRH antagonists were tested in order to delay and/or synchronise ovulation in mares. Five mares received Antarelix (0.01 mg.kg(-1)), 5 mares received Cetrorelix (the same dose), 5 mares (control mares) received the vehicle intravenously, twice daily, for 8 days from the day the largest follicle reached 22 mm following prostaglandin administration. Ovulation was postponed in all mares injected with Antarelix (19.4 +/- 1.2 days after the beginning of the treatment) and in 2/5 mares injected with Cetrorelix (20 +/- 1 days) vs. 6.2 +/- 0.4 days in control mares. During the trea...
Induction of hyaluronan synthase 2 by human chorionic gonadotropin in mural granulosa cells of equine preovulatory follicles.
Endocrinology    October 26, 2002   Volume 143, Issue 11 4375-4384 doi: 10.1210/en.2002-220563
Stock AE, Bouchard N, Brown K, Spicer AP, Underhill CB, Doré M, Sirois J.In contrast to other species, the preovulatory rise in gonadotropins in mares causes a remarkable expansion of the entire granulosa cell layer in vivo, suggesting that hyaluronan (HA) synthesis may be regulated in mural granulosa cells in this species. The objectives of this study were to clone and characterize equine hyaluronan synthase 2 (HAS2) and investigate the regulation of its transcript and of HA synthesis in equine follicles during human chorionic gonadotropin (hCG)- induced ovulation. Results showed that the equine HAS2 cDNA contains a 5'-untranslated region of 436 bp, an open readin...
Concentrations of inhibin, progesterone and oestradiol in fluid from dominant and subordinate follicles from mares during spring transition and the breeding season.
Animal reproduction science    October 16, 2002   Volume 74, Issue 1-2 55-67 doi: 10.1016/s0378-4320(02)00170-7
Watson ED, Thomassen R, Steele M, Heald M, Leask R, Groome NP, Riley SC.Dominant and subordinate follicles were collected from mares on the day after the dominant follicle reached 30 mm in diameter, to investigate regulation of folliculogenesis during spring transition and the breeding season. Concentrations of oestradiol-17beta, progesterone and inhibin A, but not inhibin isoforms with pro- and alpha C-immunoreactivity, were significantly higher in preovulatory follicles than in dominant anovulatory transitional follicles. Steroidogenic activity was regained gradually in the dominant follicles of successive anovulatory waves through spring transition. The dominan...
Proteins and enzymes in uterine lavage fluid of postpartum and nonparturient mares.
Reproduction in domestic animals = Zuchthygiene    October 2, 2002   Volume 37, Issue 5 261-268 doi: 10.1046/j.1439-0531.2002.00315.x
Reilas T, Katila T.Uterine lavage fluids from postpartum and nonparturient mares were compared to determine when the normal secretory capacity of the postpartum uterus is restored. Lavage fluids were obtained from cyclic nonparturient mares on the second, fourth or fifth day of oestrus, and 3, 8, or 14 days after ovulation (seven mares/sampling day). Twelve intact postpartum mares were sampled 1 to 28 days postpartum (group A: 1, 6, 12 and 20; group B: 2, 8, 14 and 24; group C: 4, 10, 16 and 28 days postpartum; four mares/group). Three ovariectomized (OVX) postpartum mares were sampled as mares in group C. Sampl...
Removal of deslorelin (Ovuplant) implant 48 h after administration results in normal interovulatory intervals in mares.
Theriogenology    September 6, 2002   Volume 58, Issue 5 865-870 doi: 10.1016/s0093-691x(02)00923-8
McCue PM, Farquhar VJ, Carnevale EM, Squires EL.Deslorelin implants, approved for use in inducing ovulation in mares, have been associated with prolonged interovulatory intervals in some mares. Administration of prostaglandins in the diestrous period, following a deslorelin-induced ovulation, has been reported to increase the incidence of delayed ovulations. The goals of the present study were: (1) to determine the percentage of mares given deslorelin that experience delayed ovulations with or without subsequent prostaglandin treatment, and (2) to determine if removal of the implant 48 h after administration would effect the interval to sub...
Effect of nitric oxide synthase inhabitors on ovulation in hCG-stimulated mares.
Theriogenology    September 6, 2002   Volume 58, Issue 5 1017-1026 doi: 10.1016/s0093-691x(02)00932-9
Pinto CR, Paccamonti DL, Eilts BE, Short CR, Godke RA.Recent studies suggest that nitric oxide (NO) may have a role in regulating ovarian physiology. To investigate the role of NO during ovulation in mares, inhibitors of the nitric oxide synthase (NOS) were administered to estrous mares. Forty cycling mares (20 horses and 20 pony mares) were allotted to one of the three treatment groups. Once a follicle was at least 27 mm in diameter, but smaller than 35 mm, mares were given one of the following treatments: saline solution 0.9% (n = 20, w/v, i.v., every 12 h), Nomega-nitro-L-arginine methyl ester hydrochloride (L-NAME; n = 10, 148 micromol/kg, i....
Effects of deslorelin or hCG administration on reproductive performance in first postpartum estrus mares.
Theriogenology    August 17, 2002   Volume 58, Issue 1 165-169 doi: 10.1016/s0093-691x(02)00912-3
Blanchar TL, Brinsko SP, Rigby SL.A tendency for deslorelin implants to suppress subsequent follicular growth and delay return to estrus following induced ovulation has been documented in nonlactating mares. To investigate this phenomenon in lactating mares, 22 broodmares in southeast Texas were administered either deslorelin or hCG to induce ovulation in the first postpartum estrus during February and March 2001. Mares were teased daily and examined twice weekly (Tuesdays and Thursdays) by transrectal ultrasonography. When a follicle >35 mm diameter was detected on Tuesday, mares were treated with either 2,500 U hCG admini...
Strategies to improve the ovarian response to equine pituitary extract in cyclic mares.
Theriogenology    August 17, 2002   Volume 58, Issue 1 151-164 doi: 10.1016/s0093-691x(02)00902-0
Scoggin CF, Meira C, McCue PM, Carnevale EM, Nett TM, Squires EL.Equine pituitary extract (EPE) has been reported to induce heightened follicular development in mares, but the response is inconsistent and lower than results obtained in ruminants undergoing standard superovulatory protocols. Three separate experiments were conducted to improve the ovarian response to EPE by evaluating: (1) effect of increasing the frequency or dose of EPE treatment; (2) use of a potent gonadotropin-releasing hormone agonist (GnRH-a) prior to EPE stimulation; (3) administration of EPE twice daily in successively decreasing doses. In the first experiment, 50 mares were randoml...
Analysis of the variations of follicular fluid composition during follicular growth and maturation in the mare using proton nuclear magnetic resonance (1H NMR).
Reproduction (Cambridge, England)    July 27, 2002   Volume 124, Issue 2 241-248 doi: 10.1530/rep.0.1240241
Gérard N, Loiseau S, Duchamp G, Seguin F.Follicular development and ovulatory processes in mammals involve local biochemical changes as a result of substantial modifications in cellular metabolism, the most well known of which is steroid variation. In the present study, the intrafollicular variation of several other components was studied using proton nuclear magnetic resonance ((1)H NMR). This approach made it possible to demonstrate that the intrafollicular biochemical content changes during follicular growth and maturation. Follicular fluid was aspirated by ovarian puncture of the dominant follicle at various physiological stages ...
Deslorelin acetate (Ovuplant) therapy in cycling mares: effect of implant removal on FSH secretion and ovarian function.
Equine veterinary journal    July 16, 2002   Volume 34, Issue 4 417-420 doi: 10.2746/042516402776249227
Farquhar VJ, McCue PM, Carnevale EM, Nett TM, Squires EL.Following induction of ovulation with deslorelin acetate (Ovuplant), gonadotrophin concentrations are reduced in the subsequent cycle, leading to increased interovulatory intervals in some mares. This study determined whether implant removal after 2 days prevented the decrease in gonadotrophin concentrations and follicular growth during the ensuing cycle. Twenty-four mares were randomised equally into 3 groups. Group 1 ovulated spontaneously, Groups 2 and 3 received the deslorelin implant to induce ovulation. Two days after treatment, the implant was removed from Group 3. On Day 10 postovulati...
Uterine and ovarian blood flow during the estrous cycle in mares.
Theriogenology    June 18, 2002   Volume 57, Issue 8 2129-2138 doi: 10.1016/s0093-691x(02)00703-3
Bollwei H, Weber F, Kolberg B, Stolla R.Uterine and ovarian blood flow was investigated in four mares during two consecutive estrous cycles using transrectal color Doppler sonography. The uterine and ovarian arteries of both sides were scanned to obtain waves of blood flow velocity. The pulsatility index (PI) reflected blood flow. There were significant time trends in PI values of all uterine and ovarian blood vessels during the estrous cycle (P < 0.05). PI values did not differ between the uterine arteries ipsi- and contralateral to the corpus luteum or the ovulatory follicle. PI values of the uterine arteries showed a wave shap...
Mechanisms responsible for increase in circulating inhibin levels at the time of ovulation in mares.
Theriogenology    May 31, 2002   Volume 57, Issue 6 1707-1717 doi: 10.1016/s0093-691x(02)00683-0
Nambo Y, Nagaoka K, Tanaka Y, Nagamine N, Shinbo H, Nagata S, Yoshihara T, Watanabe G, Groome NP, Taya K.In female mammals, inhibin is secreted by the granulosa cells and selectively inhibits secretion of FSH. Although circulating immunoreactive (ir)-inhibin levels decrease after ovulation as a result of the disappearance of its main source, they abruptly increase at the time of ovulation in mares. To investigate the mechanisms responsible for this increase, 50 ml of equine follicular fluid (eFF) was administered into the abdominal cavity of mares during the luteal phase (eFF, n = 4). One hour after treatment, plasma levels of ir-inhibin and inhibin pro-alphaC (but not estradiol-17beta) were sign...
Immunization against gnRH in mature mares: antibody titres, ovarian function, hormonal levels and oestrous behaviour.
Journal of veterinary medicine. A, Physiology, pathology, clinical medicine    May 22, 2002   Volume 49, Issue 3 125-131 doi: 10.1046/j.1439-0442.2002.00427.x
Dalin AM, Andresen O, Malmgren L.The aim of the present study was to investigate the effect of active immunization against GnRH in mature Standardbred mares (three experimental and one control mare) on antibody titres, ovarian function, hormonal levels and oestrous behaviour. The mares were individually teased with a stallion once each day. During the first part of the experiment (period I: late April until November), blood was sampled every third day during the first 3 months, thereafter once per week. In the second part of the experiment (period II: December until August), sampling was carried out every second week. Progest...
Administration of sulpiride to anovulatory mares in winter: effects on prolactin and gonadotropin concentrations, ovarian activity, ovulation and hair shedding.
Theriogenology    May 10, 2002   Volume 57, Issue 2 963-976 doi: 10.1016/s0093-691x(01)00696-3
Donadeu FX, Thompson DL.Sixteen seasonally anovulatory mares were randomly allotted to two groups and injected daily with either sulpiride (1 mg/kg body weight) or vehicle from 14 January to 14 February. Sulpiride administration increased daily plasma prolactin concentrations (P < 0.05), although the prolactin response during the 6 h following sulpiride injections decreased markedly from the 1st to the 6th day of treatment (treatment by day, P 0.1). Injection of GnRH and TRH on 15 February showed that the response of plasma prolactin to secretagogue was increased in sulpiride-treated mares (P 0.1) of sulpiride t...
Uterine involution, day and variance of first postpartum ovulation in mares treated with progesterone and estradiol-17beta for 1 or 2 days postpartum.
Theriogenology    May 7, 2002   Volume 57, Issue 2 989-995 doi: 10.1016/s0093-691x(01)00703-8
Bruemmer JE, Brady HA, Blanchard TL.The effects of a single or double regimen of exogenous progesterone and estradiol-17beta (P/E, total dose 300 mg P/20 mg E) were investigated in 50 postparturient Quarter Horse mares. In Trial 1, at 1 and 24 h after foaling, mares were injected with progesterone (150 mg) and estradiol-17beta (10 mg) (n = 7) or 0.9% NaCl (control, n = 13). In Trial 2, within 12 h after foaling, mares were injected with progesterone (300 mg) and estradiol-17beta (20 mg) (n = 13) or 0.9% NaCl (control, n = 17). Mares were examined daily by palpation per rectum and transrectal ultrasonography to determine the day ...
Plasma FSH, inhibin A and inhibin isoforms containing pro- and -alphaC during winter anoestrus, spring transition and the breeding season in mares.
Reproduction (Cambridge, England)    March 27, 2002   Volume 123, Issue 4 535-542 
Watson ED, Heald M, Tsigos A, Leask R, Steele M, Groome NP, Riley SC.Ten mares were studied from February (winter anoestrus) to their second ovulation in the breeding season to investigate the relationship between resumption of ovarian cyclicity in the spring and circulating concentrations of FSH, inhibin A and inhibin isoforms containing pro- and -alphaC immunoreactivity. An additional four mares were studied during one oestrous cycle. Growth and regression of ovarian follicles were monitored by transrectal ultrasonography. The frequency of blood sampling varied from three times a week to once a day, depending on the follicular activity present. Concentrations...
Successful production of offspring after superovulation and in vitro culture of embryos from domestic ferrets (Mustela putorius furos).
Reproduction (Cambridge, England)    January 31, 2002   Volume 122, Issue 4 611-618 
Li ZY, Jiang QS, Zhang YL, Liu XM, Engelhardt JF.In an effort to expand the use of ferrets as models for genetic disease, several experimental parameters that are required for successful genetic manipulation in this species were investigated. Optimum superovulation (19.3 +/- 0.6 oocytes and embryos per female) was achieved after injections of 100 iu equine chorionic gonadotrophin (eCG) and 150 iu human chorionic gonadotrophin (hCG). The ovulation rate achieved by the treatment was more than double that induced by mating. Mating with a male immediately after hCG treatment did not significantly alter the number of oocytes ovulated or the numbe...
Management and fertility of mares bred with frozen semen.
Animal reproduction science    December 18, 2001   Volume 68, Issue 3-4 219-228 doi: 10.1016/s0378-4320(01)00158-0
Samper JC.Semen quality, mare status and mare management during estrus will have the greatest impact on pregnancy rates when breeding mares with frozen semen. If semen quality is not optimal, mare selection and reproductive management are crucial in determining the outcome. In addition to mare selection, client communication is a key factor in a frozen semen program. Old maiden mares and problem mares should be monitored for normal cyclicity and all, except young maidens, should have at least a uterine culture and cytology performed. Mares with positive bacterial cultures and cytologies should be treate...
The application of three-dimensional internal structure microscopy in the observation of mare ovary.
Anatomia, histologia, embryologia    November 2, 2001   Volume 30, Issue 5 309-312 doi: 10.1046/j.1439-0264.2001.00335.x
Kimur J, Tsukise A, Yokota H, Nambo Y, Higuchi T.The ovary of the mare has a unique structure which differs totally from that of other mammals. However, because of its relatively large size, conventional histological techniques were unsuitable for the observation of the internal structure of the whole ovary. Three-dimensional internal structure microscopy (3D-ISM) consists of a cryotome-CCD camera-laser disc recorder-PC-based control system coupled with a graphic workstation. The internal structure of the ovary is observed by processing over more than 1,000 stored images of serially sliced surfaces of each frozen equine ovary. The 3D reconst...
Ovarian superstimulatory response and embryo production in mares treated with equine pituitary extract twice daily.
Theriogenology    October 23, 2001   Volume 56, Issue 5 879-887 doi: 10.1016/s0093-691x(01)00615-x
Alvarenga MA, McCue PM, Bruemmer J, Neves Neto JR, Squire EL.Equine pituitary extract (EPE), has been reported to induce multiple ovulation in mares, however ovulation rates are poor in comparison to those obtained in other species. Attempts to improve the effectiveness of EPE for induction of superovulation in cyclic mares has focused on daily frequency of EPE treatment. Two experiments were performed to compare the ovarian response of cyclic mares given EPE once or twice-daily. Mares were assigned to one of two treatment groups 6 to 8 days after ovulation: prostaglandin was given once and EPE (25 mg) was given once daily (Group 1) or twice daily (Grou...
Luteal and clinical response following administration of dinoprost tromethamine or cloprostenol at standard intramuscular sites or at the lumbosacral acupuncture point in mares.
American journal of veterinary research    August 11, 2001   Volume 62, Issue 8 1285-1289 doi: 10.2460/ajvr.2001.62.1285
Nie GJ, Goodin AN, Braden TD, Wenzel JG.To determine whether administration of a microdose of prostaglandin at the BAI HUI acupuncture point offers any advantage over IM injections for luteolysis, ovulatory interval, or systemic response in mares. Methods: 17 mature cycling mares, 3 to 20 years of age and weighing 400 to 500 kg. Methods: Conventional and microdoses of the prostaglandin dinoprost tromethamine (PGF2alpha), the analogue cloprostenol, or sterile water (control) were administered to mares in 7 treatment groups. Treatments were assigned by dose, administration site (semimembranosus, semitendinosus, or lumbosacral region),...
Effect of periovulatory prostaglandin F2alpha on pregnancy rates and luteal function in the mare.
Theriogenology    June 21, 2001   Volume 55, Issue 9 1891-1899 doi: 10.1016/s0093-691x(01)00530-1
Troedsson MH, Ababneh MM, Ohlgren AF, Madill S, Vetscher N, Gregas M.The objective of this study was to determine whether periovulatory treatments with PGF2alpha affects the development of the CL, and whether the treatment was detrimental to the establishment of pregnancy. Reproductively sound mares were assigned randomly to one of the following treatment groups during consecutive estrus cycles: 1. 3,000 IU hCG within 24 hours before artificial insemination and 500 microg cloprostenol (PGF2alpha analogue) on Days 0, 1, and 2 after ovulation (n=8), 2. 2 mL sterile water injection within 24 hours before artificial insemination and 500 microg cloprostenol on Days ...
Induction of luteolysis in mares by ultrasound-guided intraluteal treatment with PGF2alpha.
Theriogenology    June 21, 2001   Volume 55, Issue 9 1769-1776 doi: 10.1016/s0093-691x(01)00519-2
Weber JA, Causey RC, Emmans EE.To evaluate the technique of ultrasound-guided luteal injection in mares, PGF2alpha was administered under ultrasound guidance to horse mares (n = 7 to 9 per group) on Day 9 postovulation via either a systemic (i.m.; zero, 0.01, 0.1, or 5 mg/dose) route or a local intraluteal (i.l.; zero, 0.01 or 0.1 mg/dose) route. The luteolytic efficacy of each treatment was determined based on post-treatment decreases in progesterone concentration, interval to uterine edema (IE) and interovulatory interval (IOI). Local administration of PGF2alpha directly into the CL consistently induced luteolysis, at dos...
Effect of low-dose zearalenone exposure on luteal function, follicular activity and uterine oedema in cycling mares.
Acta veterinaria Hungarica    June 14, 2001   Volume 49, Issue 2 211-222 doi: 10.1556/004.49.2001.2.11
Juhász J, Nagy P, Kulcsár M, Szigeti G, Reiczigel J, Huszenicza G.The effect of 10-day zearalenone administration starting 10 days after ovulation was studied in 6 cycling trotter mares in the summer period. After an entire oestrous cycle (Cycle 1), mares were given 7 mg purified zearalenone per os daily (1 mg/ml in ethyl alcohol) beginning on Day 10 of Cycle 2. Toxin exposure was continued until the subsequent ovulation. Luteal function and follicular activity were monitored daily by rectal palpation, ultrasonography and blood sampling for progesterone. During toxin exposure, all animals were in good physical condition. The toxin had no effect on the length...
Use of buserelin to induce ovulation in the cyclic mare.
Theriogenology    June 8, 2001   Volume 55, Issue 8 1679-1695 doi: 10.1016/s0093-691x(01)00512-x
Barrier-Battut I, Le Poutre N, Trocherie E, Hecht S, Grandchamp des Raux A, Nicaise JL, Vérin X, Bertrand J, Fiéni F, Hoier R, Renault A, Egron L....Inducing ovulation in a cyclic mare is often necessary. For this purpose, hCG has been used commonly, but the response can be reduced after successive administrations. The aims of this study were to test the effectiveness of buserelin in hastening ovulation in estrus mares, and its influence on fertility; and to investigate the effect of treatment on LH secretion. Five crossover trials were designed to compare the effect of two treatments: buserelin (40 microg in 4 doses i.v. at 12 h intervals) vs placebo (Experiments 1 and 2); buserelin 40 microg (in 4 doses i.v.) vs 20 microg (Experiment 3);...
Effect of number and diameter of follicles on plasma concentrations of inhibin and FSH in mares.
Reproduction (Cambridge, England)    May 25, 2001   Volume 121, Issue 6 897-903 
Donadeu FX, Ginther OJ.The role of the number of follicles and circulating immunoreactive inhibin in the decrease in plasma FSH concentrations that occurs during development of a follicular wave was studied in mares. All follicles > or = 6 mm in diameter were ablated by ultrasound-guided transvaginal aspiration of follicular fluid on day 10 after ovulation. During the subsequent wave, all follicles, the three largest follicles (three follicle group), the largest follicle (single follicle group) or no follicles were retained and the remaining follicles were ablated before they reached > 10 mm in diameter (n = 1...
Effects of relaxin on matrix remodeling enzyme activity of cultured equine ovarian stromal cells.
Animal reproduction science    May 12, 2001   Volume 66, Issue 3-4 239-255 doi: 10.1016/s0378-4320(01)00100-2
Song L, Ryan PL, Porter DG, Coomber BL.Relaxin participates in extracellular matrix (ECM) remodeling in many reproductive organs, including the ovary, by regulating proteolytic enzyme activity. Accumulated evidence indicates this action of relaxin is involved in ovarian follicle development and ovulation. Equine follicles are embedded in cortex that is at the center of the ovary and they must expand/emigrate to the fossa, the only site in the ovary for ovulation. Due to the tremendous expansion of the follicle in this species, we hypothesized that ovarian stromal remodeling would be extensive. Therefore, cultured equine ovarian str...
1 12 13 14 15 16 28