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Theriogenology.

Periodical
Reproductive Medicine
Veterinary Medicine
Animal Population Groups
Animals
Pregnancy Complications
Reproduction
Publisher:
Geron-X.. [New York, N.Y.?] : Elsevier
Frequency: Sixteen no. a year
Country: United States
Language: English
Start Year:1974 -
ISSN:
0093-691X (Print)
1879-3231 (Electronic)
0093-691X (Linking)
Impact Factor
2.8
2022
NLM ID:0421510
(OCoLC):02504829
(DNLM):T08780000(s)
Coden:THGNBO
Classification:W1 TH677K
Regulation of ovarian follicular dynamics in farm animals. Implications for manipulation of reproduction.
Theriogenology    May 1, 2001   Volume 55, Issue 6 1211-1239 doi: 10.1016/s0093-691x(01)00479-4
Driancourt MA.In this review, the main features of folliculogenesis are summarized and compared among species. In the past few years, ultrasonography has clarified follicle growth patterns, and our understanding of follicle maturation has improved considerably. As the follicles develop towards the ovulatory stage, three features appear to be highly conserved across all species: 1) the sequence of events (recruitment, selection and dominance); 2) the sequential need for gonadotropins (FSH for recruitment, LH for dominance) and 3) the large variability of numerical parameters (number of waves per cycle, numbe...
SRY-negative XX sex reversal in a pony: a case report.
Theriogenology    April 27, 2001   Volume 55, Issue 5 1051-1057 doi: 10.1016/s0093-691x(01)00465-4
Vaughan L, Schofield W, Ennis S.A three year old pony with sexually ambiguous external genitalia was found to have a normal female karyotype (64, XX) and bilateral inguinal testes. The PCR analysis of blood samples revealed the absence of the Y chromosome sequences SRY, eTSPY and ZFY. No Y chromosome sequences were identified in DNA extracted from the gonads. The mechanism whereby XX sex reversal occurs in the absence of SRY is unknown.
Effects of estradiol-17beta administration on steady-state messenger ribonucleic acid (MRNA) encoding equine alpha and LH/CGbeta subunits in pituitaries of ovariectomized pony mares.
Theriogenology    April 27, 2001   Volume 55, Issue 5 1083-1093 doi: 10.1016/s0093-691x(01)00468-x
Sharp DC, Wolfe MW, Cleaver BD, Nilson J.The process of sexual recrudescence in the springtime in mares is characterized by renewal of follicular growth and acquisition of steroidogenic competence. Concomitant with renewal of follicular steroidogenesis is re-establishment of LH biosynthesis and secretion. Research results from our laboratory indicate that increased estradiol and LH secretion occur in close temporal association before the first ovulation of the year. Therefore, the hypothesis tested in this experiment was that estrogen administration to ovariectomized pony mares during the equivalent time of early vernal transition wo...
Changes in plasma gonadotrophin and prolactin concentrations following castration of the pony stallion.
Theriogenology    April 27, 2001   Volume 55, Issue 5 1171-1180 doi: 10.1016/s0093-691x(01)00475-7
Collingsworth MG, Fuller Z, Cox JE, Argo CM.Concentrations of gonadotrophins and prolactin were recorded in pony stallions castrated during the early breeding season, to examine the regulatory role of the gonad at a time when testosterone has been postulated to exert positive feedback on LH secretion. Further, gonadotrophin concentrations in geldings are reported to return to values within the normal range of the entire stallion. In an attempt to characterize this species-specific reversal, the gonadotrophin concentrations of 6 male ponies castrated on 25 March were monitored for 4 months, and 4 stallions were used to generate control d...
Effects of ovarian input on GnRH and LH secretion immediately postovulation in pony mares.
Theriogenology    April 27, 2001   Volume 55, Issue 5 1095-1106 doi: 10.1016/s0093-691x(01)00469-1
Greaves HE, Kalariotes V, Cleaver BD, Porter MB, Sharp DC.The potential involvement of ovarian factors in regulating GnRH and LH postovulation was studied in ovarian intact (Group 1; n=3) and ovariectomized (OVX; Group 2; n=3) mares (OVX within 12 hr of ovulation). Blood samples were collected every 10 min for 6 hr from jugular vein (JV) and intercavernous sinus (ICS) during estrus and on Day 8 postovulation for LH and GnRH analysis. Additionally, JV samples were collected twice daily (12-hr intervals) for 30 days for LH and progesterone (P4) analysis. A significant treatment x day effect (P<0.0001) describes declining plasma LH concentrations in ...
Testicular concentration of meiosis-activating sterol is associated with normal testicular descent.
Theriogenology    April 9, 2001   Volume 55, Issue 4 983-992 doi: 10.1016/s0093-691x(01)00459-9
Bøgh IB, Baltsen M, Byskov AG, Greve T.In the cryptorchid stallion, spermatogenesis is arrested at various levels before the completion of meiosis. In men, infantile cryptorchidism is also often associated with oligo- and azoospermia during adulthood. An impairment of spermatogenesis might be reflected in the level of locally produced factors. Formerly, a meiosis-activating sterol (T-MAS) has been isolated in murine and bovine testes. This sterol possesses the potential to trigger resumption of meiosis in cultured mouse oocytes, indicating that it might play an important role in the regulation of the meiotic process in the female g...
Adaptation of the hypoosmotic swelling test to assess functional integrity of stallion spermatozoal plasma membranes.
Theriogenology    April 9, 2001   Volume 55, Issue 4 1005-1018 doi: 10.1016/s0093-691x(01)00461-7
Nie GJ, Wenzel JG.Hypoosmotic swelling (HOS) is used for assessing plasma membrane function and fertilizing capacity of human spermatozoa. However, HOS solutions and methodologies have not been evaluated specifically for assessing stallion spermatozoa. The objective of this study was to identify a HOS solution and assay conditions specifically for stallions that would maximize spermatozoal plasma membrane swelling. The HOS solutions and assay conditions, including incubation time (15 to 180 min), temperature (25 degrees vs 37 degrees C), and total number of cells examined (100, 200 or 500) were evaluated. Assay...
Embryo development rates after transfer of oocytes matured in vivo, in vitro, or within oviducts of mares.
Theriogenology    March 14, 2001   Volume 55, Issue 3 705-715 doi: 10.1016/s0093-691x(01)00438-1
Scott TJ, Carnevale EM, Maclellan LJ, Scoggin CF, Squires EL.Objectives of the present study were to use oocyte transfer: 1) to compare the developmental ability of oocytes collected from ovaries of live mares with those collected from slaughterhouse ovaries; and 2) to compare the viability of oocytes matured in vivo, in vitro, or within the oviduct. Oocytes were collected by transvaginal, ultrasound-guided follicular aspiration (TVA) from live mares or from slicing slaughterhouse ovaries. Four groups of oocytes were transferred into the oviducts of recipients that were inseminated: 1) oocytes matured in vivo and collected by TVA from preovulatory folli...
Influence of Eqvalan (ivermectin) on quality and freezability of stallion semen.
Theriogenology    March 14, 2001   Volume 55, Issue 3 785-792 doi: 10.1016/s0093-691x(01)00443-5
Janett F, Thun R, Ryhiner A, Burger D, Hassig M, Hertzberg H.The objective of this study was to evaluate the effect of Eqvalan (ivermectin) on stallion semen quality and freezability. Experiments were performed using 22 Freiberger stallions, randomly divided into a control and test group. Semen was collected once a week for 17 weeks from October 1997 to February 1998. Eqvalan was given orally to all stallions of the test group at a therapeutic dose of 0.2 mg ivermectin/kg. Besides measuring the scrotal width, ejaculates were collected to determine the volume, concentration, and the motility and morphology (normal sperm, major defects, vacuoles and acros...
Effect of cooling of equine spermatozoa before freezing on post-thaw motility: preliminary results.
Theriogenology    March 14, 2001   Volume 55, Issue 3 793-803 doi: 10.1016/s0093-691x(01)00444-7
Crockett EC, Graham JK, Bruemmer JE, Squires EL.The ability to ship cooled stallion semen to a facility that specializes in cryopreservation of spermatozoa would permit stallions to remain at home while their semen is cryopreserved at facilities having the equipment and expertise to freeze the semen properly. To accomplish this goal, methods must be developed to freeze cooled shipped semen. Three experiments were conducted to determine the most appropriate spermatozoal extender, package, time of centrifugation, spermatozoal concentration and length of time after collection that spermatozoa can be cooled before cryopreservation. In the first...
Cryopreservation of equine embryos by open pulled straw, cryoloop, or conventional slow cooling methods.
Theriogenology    March 10, 2001   Volume 55, Issue 2 607-613 doi: 10.1016/s0093-691x(01)00429-0
Oberstein N, O'Donovan MK, Bruemmer JE, Seidel GE, Carnevale EM, Squires EL.Cryopreservation of equine embryos with conventional slow-cooling procedures has proven challenging. An alternative approach is vitrification, which can minimize chilling injuries by increasing the rates of cooling and warming. The open pulled straw (OPS) and cryoloop have been used for very rapid cooling and warming rates. The objective of this experiment was to compare efficacy of vitrification of embryos in OPS and the cryoloop to conventional slow cool procedures using 0.25 mL straws. Grade 1 or 2 morulae and early blastocysts ( 0.1) in morphological grade or percent live cells among metho...
Expression of 3beta-hydroxysteroid dehydrogenase, cytochrome p450 17alpha-hydroxylase/17,20-lyase and cytochrome p450 aromatase enzymes in corpora lutea of diestrous and early pregnant mares.
Theriogenology    March 10, 2001   Volume 55, Issue 2 551-561 doi: 10.1016/s0093-691x(01)00425-3
Albrecht BA, MacLeod JN, Daels PF.In the pregnant mare, luteal estrogen production increases at the onset of equine chorionic gonadotropin (eCG) secretion by endometrial cups. In previous studies, we have demonstrated that eCG stimulates luteal androgen and estrogen production in pregnant mares. To further elucidate the regulation of steroidogenesis within the equine corpus luteum (CL) of pregnancy, we examined the expression of 3beta-hydroxysteroid dehydrogenase (3beta-HSD), cytochrome P450 17alpha-hydroxylase/17,20 lyase (P450(17alpha)) and cytochrome P450 aromatase (P450(arom)) in luteal tissue samples collected during dies...
Treatments resulting in pregnancy in nonovulating, hormone-treated oocyte recipient mares.
Theriogenology    February 24, 2001   Volume 54, Issue 8 1285-1293 doi: 10.1016/s0093-691x(00)00435-0
Hinrichs K, Provost PJ, Torello EM.Synchronization of follicle growth between oocyte donor and recipient mares is difficult. To avoid this, recipient mares in a clinical program were used during a period of low follicular activity, and were treated with estrogen before transfer and progesterone after transfer. Five pregnancies were established after oocyte transfer to nonovulating, hormone-treated recipient mares. One pregnancy was lost before 30 d gestation, and the other 4 foals were carried to term. One foal died at birth. Establishment and maintenance of pregnancy in these mares indicates that nonovulating, hormone-treated ...
Assessment of stallion spermatozoa viability by flow cytometry and light microscope analysis.
Theriogenology    February 24, 2001   Volume 54, Issue 8 1215-1224 doi: 10.1016/s0093-691x(00)00428-3
Merkies K, Chenier T, Plante C, Buhr MM.Viability of spermatozoa can be assessed by numerous methods, but many are slow and poorly repeatable, and subjectively assess only 100 to 200 spermatozoa per ejaculate. We collected two ejaculates from each of 4 stallions, and extended them to 50x10(6) sperm/mL in a nonfat dried milk solids glucose extender (EZ Mixin). Half the ejaculate was freeze-killed by immersing in liquid nitrogen for 10 min. Aliquots using appropriate volumes of live and freeze-killed spermatozoa provided the following ratios of live:dead spermatozoa: 100:0, 75:25, 50:50, 25:75, 0:100. We determined the viability of ea...
Significance of plasmalemma disruption in bovine and equine spermatozoa.
Theriogenology    December 29, 2000   Volume 54, Issue 7 1075-1086 doi: 10.1016/s0093-691x(00)00416-7
Abraham-Peskir JV, Chantler E, Uggerhøj E.We have investigated fresh and cryopreserved bovine and equine spermatozoa using light and transmission soft X-ray microscopy. Spermatozoa were examined, in the presence or absence of semen, after using Percoll gradient centrifugation and re-suspending in medium. X-ray microscopy provided high resolution (30 nm) transmission images of whole cells in solution with high contrast, while retaining the simple preparation techniques used in light microscopy. We demonstrated translucent, membrane-bound vesicles in the acrosomal and midpiece regions that were similar in size and we noted their inciden...
The use of pentoxifylline to improve motility of cryopreserved equine spermatozoa.
Theriogenology    December 29, 2000   Volume 54, Issue 7 1041-1047 doi: 10.1016/s0093-691x(00)00412-x
Gradil CM, Ball BA.Pentoxifylline was evaluated as a method to increase motility of cryopreserved equine spermatozoa. In a preliminary experiment, pentoxifylline (3.5 mM or 7.0 mM) was added to extended semen that was chilled to 4 degrees C. Motility was evaluated at 8-h intervals for 48 h. The addition of 3.5 or 7.0 mM pentoxifylline appeared to increase the motility of chilled spermatozoa compared to controls. Based on these results, similar concentrations of pentoxifylline were added to semen either before or after cryopreservation. The addition of pentoxifylline (3.5 or 7.0 mM) to semen before cryopreservati...
Comparison of culture and insemination techniques for equine oocyte transfer.
Theriogenology    November 30, 2000   Volume 54, Issue 6 981-987 doi: 10.1016/S0093-691X(00)00406-4
Carnevale EM, Maclellan LJ, Coutinho da Silva MA, Scott TJ, Squires EL.This study was designed to test 3 approaches for insemination and transfer of oocytes to recipient mares. Oocytes were recovered transvaginally from naturally cycling donor mares 24 to 26 h after an intravenous injection of 2500 IU of hCG when follicles reached 35 mm in diameter. Multiple oocytes (1 to 4) were transferred surgically into the oviducts of 4 or 5 recipient mares per group. Three groups of transfers were compared: 1) transfer of oocytes cultured in vitro for 12 to 14 h postcollection with insemination of the recipient 2 h postsurgery; 2) transfer of oocytes into the oviduct within...
Centrifugation and addition of glycerol at 22 degres C instead of 4 degrees C improve post-thaw motility and fertility of stallion spermatozoa.
Theriogenology    November 30, 2000   Volume 54, Issue 6 907-919 doi: 10.1016/s0093-691x(00)00401-5
Vidament M, Ecot P, Noue P, Bourgeois C, Magistrini M, Palmer E.The aims of this study were to evaluate the effects of cooling rate to 4 degrees C and temperature at the time of centrifugation/glycerol-addition (freezing extender: INRA82 + 2% egg yolk + 2.5% glycerol) on postcentrifugation recovery rate, post-thaw motility and per-cycle fertility. When centrifugation/glycerol-addition was performed at 4 degrees C (14 ejaculates), a moderate cooling rate (37 degrees C to 4 degrees C in I h) resulted in higher post-thaw motility (45%) than when using a slow cooling rate (37 degrees C to 4 degrees C in 4 h) (39%; P<0.05). When centrifugation/glycerol-addit...
Factors affecting pregnancy rates and early embryonic death after equine embryo transfer.
Theriogenology    November 30, 2000   Volume 54, Issue 6 965-979 doi: 10.1016/S0093-691X(00)00405-2
Carnevale EM, Ramirez RJ, Squires EL, Alvarenga MA, Vanderwall DK, McCue PM.In the present study, 638 embryo transfers conducted over 3 yr were retrospectively examined to determine which factors (recipient, embryo and transfer) significantly influenced pregnancy and embryo loss rates and to determine how rates could be improved. On Day 7 or 8 after ovulation, embryos (fresh or cooled/transported) were transferred by surgical or nonsurgical techniques into recipients ovulating from 5 to 9 d before transfer. At 12 and 50 d of gestation (Day 0 = day of ovulation), pregnancy rates were 65.7% (419 of 638) and 55.5% (354 of 638). Pregnancy rates on Day 50 were significantl...
T-cell distribution in two different segments of the equine endometrium 6 and 48 hours after insemination.
Theriogenology    November 30, 2000   Volume 54, Issue 6 835-841 doi: 10.1016/s0093-691x(00)00395-2
Tunón A-M , Katila T, Magnusson U, Nummijärvi A, Rodriguez-Martinez H.The T-cell response after the introduction of semen into the uterine cavity in the mare was studied by examining, immunohistochemically, the distribution of helper T-cells (CD4+) and cytotoxic T-cells (CD8+) in endometrial biopsy specimens. Endometrial tissue samples were obtained from twenty-five gynecologically healthy mares during estrus before and 6 or 48 h after deposition of a single dose of stallion semen. An increase (P=0.04) in the number of helper T-cells (CD4+) compared to pre-insemination values was observed in the uterine body in both groups, 6 and 48 h, after insemination. No sig...
Control of follicular development and luteal function in the mare: effects of a GnRH antagonist.
Theriogenology    November 9, 2000   Volume 54, Issue 4 599-609 doi: 10.1016/S0093-691X(00)00375-7
Watson ED, Pedersen HG, Thomson SR, Fraser HM.Control of the equine estrous cycle was studied by suppressing gonadotropin secretion by administration of a GnRH antagonist to cyclic pony mares. Four mares received vehicle (control cycle) or a GnRH antagonist, Antarelix (100 microg/kg) on Day 8 of diestrus, and blood samples were collected at 15-min intervals from 0 to 16 h, 24 to 36 h, and daily until the next ovulation. Ovarian activity was monitored by transrectal ultrasonography, and measurement of plasma concentrations of progesterone and estradiol. Antagonist treatment eliminated large diestrous pulses of LH. Progesterone concentratio...
Effect of dose and day of treatment on uterine response to oxytocin in mares.
Theriogenology    October 29, 2000   Volume 54, Issue 3 447-456 doi: 10.1016/S0093-691X(00)00361-7
Gutjahr S, Paccamonti DL, Pycock JF, Taverne MA, Dieleman SJ, van der Weijden GC.To determine the effect of dose and day of oxytocin treatment on intrauterine pressure, 6 normal mares were treated with 10 or 25 IU oxytocin 2 days before ovulation, on the day of ovulation and 2 days after ovulation. Intrauterine pressure (IUP) was measured using micro-tip-catheters (one placed intrauterine, a second and third serving as reference sensors in the vagina and external to the mare) and transmitted by telemetry for 30 min to establish a baseline before saline was administered, iv, and for an additional 30 min after saline administration. Oxytocin was then given, iv, and IUP was r...
Effect of centrifugation and partial removal of seminal plasma on equine spermatozoal motility after cooling and storage.
Theriogenology    September 16, 2000   Volume 54, Issue 1 129-136 doi: 10.1016/S0093-691X(00)00331-9
Brinsko SP, Crockett EC, Squires EL.The objective of this study was to determine if centrifugation and partial removal of seminal plasma would improve spermatozoal motility in semen from stallions whose whole ejaculates have poor tolerance to cooling and storage. Stallions were divided into two groups (n = 5/group) based on the ability of their extended semen to maintain spermatozoal motility after cooling and storage. Group 1 stallions ("good coolers") produced semen in which progressive spermatozoal motility after 24 h of cooling and storage was reduced by or = 40% of progressive motility prior to storage. The sperm-rich port...
Vitrification of immature and mature equine and bovine oocytes in an ethylene glycol, ficoll and sucrose solution using open-pulled straws.
Theriogenology    September 16, 2000   Volume 54, Issue 1 119-128 doi: 10.1016/s0093-691x(00)00330-7
Hurtt AE, Landim-Alvarenga F, Seidel GE, Squires EL.Studies were conducted to compare viability of immature and mature equine and bovine oocytes vitrified in ethylene glycol. Ficoll using open-pulled straws. Oocytes from slaughterhouse ovaries (N=50/group) with >2 layers of compact cumulus cells were vitrified immediately after collection (immature groups) or vitrified after 36 to 40 (equine) or 22 to 24 (bovine) h of maturation (mature groups). Immature oocytes were matured after thawing. Before vitrification, oocytes were exposed to TCM-199 + 10 FCS + 2.5 M ethylene glycol + 18% Ficoll + 0.5 M sucrose (EFS) for 30 sec and then to 5 M ethyl...
Effect of intrauterine treatment with prostaglandin E2 prior to insemination of mares in the uterine horn or body.
Theriogenology    September 1, 2000   Volume 53, Issue 9 1827-1836 doi: 10.1016/s0093-691x(00)00318-6
Woods J, Rigby S, Brinsko S, Stephens R, Varner D, Blanchard T.Two trials were conducted to investigate the effects of intrauterine infusion of PGE2 and uterine horn insemination on pregnancy rates in mares achieved by breeding with a suboptimal number of normal spermatozoa. Estrus was synchronized and mares were teased daily with a stallion to detect estrus. Mares in estrus were examined by transrectal palpation and ultrasonography to monitor follicular status. On the first day a 35-mm diameter follicle was present, hCG (1500 IU, iv) was administered and the mares were bred the next day. Mares (Trial 1, n = 34; Trial 2, n = 28) were inseminated with 25 m...
Assessment of equine sperm mitochondrial function using JC-1.
Theriogenology    September 1, 2000   Volume 53, Issue 9 1691-1703 doi: 10.1016/s0093-691x(00)00308-3
Gravance CG, Garner DL, Baumber J, Ball BA.The fluorescent carbocyanine dye, JC-1, labels mitochondria with high membrane potential orange and mitochondria with low membrane potential green. Evaluation of mitochondrial membrane potential with JC-1 has been used in a variety of cell types, including bull spermatozoa; however, JC-1 staining has not yet been reported for equine spermatozoa. The aim of this study was to apply JC-1 staining and assessment by flow cytometry or a fluorescence microplate reader for evaluation of mitochondrial function of equine spermatozoa. Six ejaculates from four stallions were collected and centrifuged thro...
Compartmentalization of steroidogen esis by the equine corpus luteum.
Theriogenology    July 18, 2000   Volume 53, Issue 7 1459-1466 doi: 10.1016/S0093-691X(00)00288-0
Watson ED.The presence of cytochrome P450C17 within equine follicles and corpora lutea (CL) was detected by immunostaining. Two different antibodies were used which had previously been shown by immunoblotting to cross-react with equine P450C17. Strong positive immunostaining was present in the theca-derived cells of the CL during the estrous cycle and pregnancy. In the CL from mares after Day 40 of pregnancy there were also occasional bands of positively stained cells which resembled the polyhedral-shaped theca cells seen in preovulatory follicles. The pattern of immunostaining suggested compartmentaliz...
Effects of transport container and ambient storage temperature on motion characteristics of equine spermatozoa.
Theriogenology    July 7, 2000   Volume 53, Issue 8 1641-1655 doi: 10.1016/S0093-691X(00)00304-6
Brinsko SP, Rowan KR, Varner DD, Blanchard TL.This study was conducted to compare the cooling rates and storage temperatures within equine semen transport containers exposed to different ambient temperatures, and to evaluate the ability of these containers to preserve spermatozoal motility following 24 h of storage under these conditions. In Experiment 1, nonfat dried milk solids, glucose, sucrose, equine semen extender was divided into seven 40-mL aliquots and loaded into seven different semen transport containers: Equitainer I, Equitainer II, Equitainer III, ExpectaFoal, Bio-Flite, Lane STS, and Equine Express. After containers were loa...
Insemination of mares with low numbers of either unsexed or sexed spermatozoa.
Theriogenology    June 1, 2000   Volume 53, Issue 6 1333-1344 doi: 10.1016/S0093-691X(00)00276-4
Buchanan BR, Seidel GE, McCue PM, Schenk JL, Herickhoff LA, Squires EL.Two experiments were conducted to determine pregnancy rates in mares inseminated 1) with 5, 25 and 500 x 10(6) progressively motile spermatozoa (pms), or 2) with 25 x 10(6) sex-sorted cells. In Experiment 1, mares were assigned to 1 of 3 treatments: Group 1 (n=20) was inseminated into the uterine body with 500 x 10(6) pms. Group 2 (n=21) and Group 3 (n=20) were inseminated into the tip of the uterine horn ipsilateral to the preovulatory follicle with 25 and 5 x 10(6) pms, respectively. Mares in all 3 groups were inseminated either 40 (n=32) or 34 h (n=29) after GnRH administration. More mares ...
Effect of PGF2alpha and 13,14-dihydro-15-keto-PGF2alpha (PGFM) on corpora luteal function in nonpregnant mares.
Theriogenology    June 1, 2000   Volume 53, Issue 6 1263-1271 doi: 10.1016/S0093-691X(00)00270-3
Vanderwall DK, Betschart RW, Squires EL.The objective of this study was to determine if the primary circulating metabolite of PGF2alpha, 13,14-dihydro-15-keto-PGF2alpha (PGFM), is biologically active and would induce luteolysis in nonpregnant mares. On Day 9 after ovulation, mares (n = 7/group) were randomly assigned to receive: 1) saline control, 2) 10 mg PGF2alpha or 3) 10 mg PGFM in 5 mL 0.9% sterile saline i.m. On Days 0 through 16, blood was collected for progesterone analysis. In addition, blood was collected immediately prior to treatment, hourly for 6 h, and then at 12 and 24 h after treatment for progesterone and PGFM analy...
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