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Topic:Embryo Transfer

Embryo transfer in horses is a reproductive technology that involves collecting a fertilized embryo from a donor mare and implanting it into a recipient mare, which then carries the pregnancy to term. This technique allows for the production of multiple offspring from a single mare within a breeding season. The procedure includes several stages: synchronization of the donor and recipient mares' estrous cycles, collection of the embryo, and its subsequent transfer to the recipient mare. Embryo transfer is utilized to enhance genetic dissemination, preserve valuable genetics, and manage breeding schedules. This page aggregates peer-reviewed research studies and scholarly articles that explore the methods, efficiency, and applications of embryo transfer in equine reproduction.
Equine blastocyst development after intracytoplasmic injection of sperm subjected to two freeze-thaw cycles.
Theriogenology    August 10, 2005   Volume 65, Issue 4 808-819 doi: 10.1016/j.theriogenology.2005.04.035
Choi YH, Love CC, Varner DD, Hinrichs K.This study was conducted to evaluate the effects of thawing, division into aliquots and refreezing on fertilizing capacity (ability to support embryo development after intracytoplasmic sperm injection; ICSI) of frozen stallion semen. Frozen semen from a fertile stallion was thawed, diluted 1:100 with freezing extender, and refrozen (2F treatment). Control semen was frozen only once. In vitro matured equine oocytes were injected with: (1) motile control spermatozoa; (2) motile 2F spermatozoa; (3) non-motile 2F spermatozoa; or (4) non-motile 2F spermatozoa, followed by injection of sperm extract...
The development and application of the modern reproductive technologies to horse breeding.
Reproduction in domestic animals = Zuchthygiene    July 13, 2005   Volume 40, Issue 4 310-329 doi: 10.1111/j.1439-0531.2005.00602.x
Allen WR.Although the horse was probably the first animal to experience and benefit from artificial insemination, it trailed the field somewhat with regard to the application of embryo transfer and other oocyte and embryo-related modern breeding technologies. But with a late run it is now back in mid-field and gaining fast on the other large domestic species in the application of the many technological advances of the past 20 years to sound breeding practice. Improvements in extenders and cryoprotectants have resulted in a veritable upsurge in the transport and insemination of cooled and frozen stallio...
Factors affecting the success of oocyte transfer in a clinical program for subfertile mares.
Theriogenology    June 14, 2005   Volume 64, Issue 3 519-527 doi: 10.1016/j.theriogenology.2005.05.008
Carnevale EM, Coutinho da Silva MA, Panzani D, Stokes JE, Squires EL.Oocyte transfer is a potential method to produce offspring from valuable mares that cannot carry a pregnancy or produce embryos. From 2000 through 2004, 86 mares, 19.2 +/- 0.4 yr of age (mean +/- S.E.M.), were used as oocyte donors in a clinical program at Colorado State University. Oocytes were collected from 77% (548/710) of preovulatory follicles and during 96% (548/570) of cycles. Oocytes were collected 21.0+/-0.1h after administration of hCG to estrous donors and cultured 16.4 +/- 0.2 h prior to transfer into recipients' oviducts. At 16 and 50 d after transfer, pregnancies were detected i...
In vitro comparisons of two cryopreservation techniques for equine embryos: slow-cooling and open pulled straw (OPS) vitrification.
Theriogenology    May 24, 2005   Volume 64, Issue 7 1619-1632 doi: 10.1016/j.theriogenology.2005.04.001
Moussa M, Bersinger I, Doligez P, Guignot F, Duchamp G, Vidament M, Mermillod P, Bruyas JF.Vitrification using open pulled straw (OPS) has provided encouraging results with embryos from other species. The aim of this study was to compare the survival of 6.5- and 6.75-day-old equine embryos after OPS vitrification and slow-cooling. Eighteen embryos were frozen using a slow-cooling method. Embryos were placed in modified PBS with increasing glycerol concentration (2.5%, 5%, 7.5% and 10% (v/v) 5 min each). Embryos were loaded into 0.25 ml straws then placed in a programmable freezer and subsequently plunged into liquid nitrogen. After thawing, cryoprotectant was removed by five steps w...
Cloned horse pregnancies produced using adult cumulus cells.
Reproduction, fertility, and development    March 3, 2005   Volume 16, Issue 7 675-679 doi: 10.1071/rd04025
Vanderwall DK, Woods GL, Aston KI, Bunch TD, Li G, Meerdo LN, White KL.The objectives of the present study were to: (1) clone horses using adult cumulus cells; and (2) determine whether the cumulus cell donor affected the outcome. In vivo-matured cumulus-oocyte complexes were obtained using transvaginal ultrasound-guided follicle aspiration; oocytes were used as cytoplasts, whereas cumulus cells (from one of three different mares) were used as donor cells. Immediately following nuclear transfer and activation procedures, cloned embryos were transferred surgically to the oviduct of recipient mares (n = 2-5 embryos per recipient) that had ovulated within 24 h prior...
Establishment of pregnancies after serial dilution or direct transfer by vitrified equine embryos.
Theriogenology    February 24, 2005   Volume 63, Issue 5 1308-1319 doi: 10.1016/j.theriogenology.2004.06.015
Eldridge-Panuska WD, di Brienza VC, Seidel GE, Squires EL, Carnevale EM.Experiments were conducted to determine viability of equine embryos in vivo after vitrification. In a preliminary study (Experiment 1), embryos were exposed in three steps to vitrification solutions containing increasing concentrations of ethylene glycol and glycerol (EG/G); the final vitrification solution was 3.4 M glycerol + 4.6 M ethylene glycol in a base medium of phosphate-buffered saline. Embryos were warmed in a two-step dilution and transferred into uteri of recipients. No pregnancies were observed after transfer of blastocysts >300 microm (n = 3). Transfer of morulae or blastocyst...
Stage-specific formation of the equine blastocyst capsule is instrumental to hatching and to embryonic survival in vivo.
Animal reproduction science    December 28, 2004   Volume 87, Issue 3-4 269-281 doi: 10.1016/j.anireprosci.2004.11.009
Stout TA, Meadows S, Allen WR.Early embryonic development in the horse is characterized by the formation of an unusual acellular glycoprotein "capsule" between the trophectoderm and the overlying zona pellucida. This structure is first detected between days 6 and 7 after ovulation and completely envelops the spherical conceptus until as late as day 23 of gestation. In the present study, a micromanipulator was used to remove the capsule from 15 embryos on day 6-7 after ovulation. None of these denuded embryos developed into ultrasonographically detectable pregnancies after surgical transfer into recipient mares whereas four...
Differences in the incidence of apoptosis between in vivo and in vitro produced blastocysts of farm animal species: a comparative study.
Theriogenology    November 28, 2004   Volume 63, Issue 8 2254-2268 doi: 10.1016/j.theriogenology.2004.10.015
Pomar FJ, Teerds KJ, Kidson A, Colenbrander B, Tharasanit T, Aguilar B, Roelen BA.The occurrence of pregnancies and births after embryo transfer (ET) of in vivo produced embryos is generally more successful compared to that of embryos produced in vitro. This difference in ET success has been observed when embryos of morphological equal (high) quality were used. The incidence of apoptosis has been suggested as an additional criterion to morphological embryo evaluation in order to assess embryo quality and effectively predict embryo viability. In this study, equine, porcine, ovine, caprine and bovine in vivo and in vitro produced morphologically selected high quality (grade-I...
Use of parentage testing to determine optimum insemination time and culture media for oocyte transfer in mares.
Reproduction (Cambridge, England)    October 29, 2004   Volume 128, Issue 5 623-628 doi: 10.1530/rep.1.00207
Carnevale EM, Coutinho da Silva MA, Maclellan LJ, Seidel GE, Squires EL.Parentage identification was used to test the developmental competence of oocytes cultured under different conditions and fertilized in vivo after oocyte transfer. Oocytes were collected transvaginally from follicles of estrous mares approximately 22 h after administration of human chorionic gonadotropin. Oocytes were cultured for approximately 16 h in one of three media, with or without addition of hormones and growth factors. Groups of three or four oocytes, cultured in different media, were transferred into the oviduct contralateral to a recipient's own ovulation. Recipients were inseminate...
Integration of sperm sexing technology into the ART toolbox.
Animal reproduction science    July 24, 2004   Volume 82-83 79-95 doi: 10.1016/j.anireprosci.2004.04.013
Maxwell WM, Evans G, Hollinshead FK, Bathgate R, De Graaf SP, Eriksson BM, Gillan L, Morton KM, O'Brien JK.Sex-sorting of mammalian spermatozoa has applications for genetic improvement of farm animals, in humans for the control of sex-linked disease, and in wildlife as a captive management strategy and for the re-population of endangered species. Considerable research has been undertaken worldwide on the Beltsville sperm sexing technology, the only effective method for pre-selection of sex of offspring. The combination of this method with assisted reproductive technologies has resulted in the birth of offspring in a wide range of animals, including cattle, the only livestock species in which sperm ...
Postnatal insulin secretion and sensitivity after manipulation of fetal growth by embryo transfer in the horse.
The Journal of endocrinology    June 3, 2004   Volume 181, Issue 3 459-467 doi: 10.1677/joe.0.1810459
Forhead AJ, Ousey JC, Allen WR, Fowden AL.This study examined the effects of intrauterine growth on insulin secretion and resistance in newborn foals. Embryo transfer between small pony and large Thoroughbred mares was used to produce four groups of foals with different birth weights (pony in pony n=7; pony in Thoroughbred n=7; Thoroughbred in Thoroughbred n=8; Thoroughbred in pony n=8). On day 2 after birth, glucose (0.5 g/kg) was administered intravenously to the foal and blood samples were taken for 2 h to determine plasma glucose and insulin concentrations. On day 3, insulin sensitivity was assessed by giving insulin (0.75 U/kg i....
The influence of maternal size on pre- and postnatal growth in the horse: III Postnatal growth.
Reproduction (Cambridge, England)    April 2, 2004   Volume 127, Issue 1 67-77 doi: 10.1530/rep.1.00024
Allen WR, Wilsher S, Tiplady C, Butterfield RM.The growth parameters exhibited by seven Thoroughbred (Tb) foals that had experienced a 'restricted' in utero existence following transfer as embryos to the uteri of smaller Pony (P) mares (Tb-in-P) and, conversely, six P foals that experienced a 'luxurious' in utero existence after transfer to larger Tb mares (P-in-Tb), were compared from birth to 3 years of age with those exhibited by six normal Tb-in-Tb and six P-in-P foals conceived by within-breed artificial insemination. Bodyweight, height at the withers, girth, poll-to-nose length, crown-rump length and three foreleg longbone measuremen...
In vitro maturation and transfer of equine oocytes after transport of ovaries at 12 or 22 degrees C.
Theriogenology    March 24, 2004   Volume 61, Issue 7-8 1215-1223 doi: 10.1016/j.theriogenology.2003.06.008
Preis KA, Carnevale EM, Coutinho da Silva MA, Caracciolo di Brienza V, Gomes GM, Maclellan LJ, Squires EL.Transportation of equine ovaries would allow shipment of oocytes for research purposes or transfer after the death of a valuable mare. The objective of this study was to compare two temperatures for maintaining ovaries during a transport interval of 18-24 h. The goal was to obtain pregnancies after transport of ovaries, maturation of oocytes in vitro, and transfer of oocytes. Each shipment was composed of ovaries four to seven mares collected from an abattoir. From each mare, one ovary was packaged at approximately 12 degrees C, and the other was packaged at approximately 22 degrees C. Upon ar...
Standing female equine urogenital endoscopic surgery.
The Veterinary clinics of North America. Equine practice    February 27, 2004   Volume 16, Issue 2 301-vi doi: 10.1016/s0749-0739(17)30106-2
Dechant JE, Hendrickson DA.Standing female urogenital endoscopic surgery is facilitated by the more dorsal location of the organs of the female reproduction tract. The most common reason for laparoscopic surgery on the female urogenital system is ovariectomy; however, the technique has been used to diagnose periparturient or reproductive diseases and to perform surgical embryo transfer. Standing surgical approaches avoid the risk and expense of general anesthesia, but these techniques are limited by the temperament and size of the patient and the availability of facilities for restraint. Owner acceptance of laparoscopic...
Japanese Society for Animal Reproduction: award for outstanding research 2002. Cryopreservation of follicular oocytes and preimplantation embryos in cattle and horses.
The Journal of reproduction and development    February 18, 2004   Volume 49, Issue 1 13-21 doi: 10.1262/jrd.49.13
Hochi S.Factors affecting sensitivity of preimplantation embryos and follicular oocytes to cryopreservation were analyzed in the equine and bovine species. (1) Survival of equine blastocysts after two-step freezing in the presence of glycerol as the cryoprotective agent (CPA) was influenced by development of the embryonic capsule. The use of ethylene glycol (EG) with sucrose as CPAs improved the post-thaw survival of blastocysts and made it possible to transfer the embryos into recipient mares without removing the CPAs. In addition, early blastocysts cryopreserved by vitrification could develop both i...
Ultrasonographic monitoring of 103 recipient mares of different reproductive status during the first 30 days after embryo transfers.
The Veterinary record    November 25, 2003   Volume 153, Issue 18 558-560 doi: 10.1136/vr.153.18.558
Taveiros AW, Oliveira MA, Lima PF, Tenório Filho F, Bartolomeu CC, Santos MH, Oliveira LR, Iunes-Souza TC, Freitas JC.Ten pluriparous mares were used as donors to supply embryos which were transferred into 103 recipients, 31 of which were nulliparous, 34 were pluriparous and lactating, and 38 were pluriparous and non-lactating. The embryos were recovered eight days after ovulation and pregnancy was confirmed by ultrasound six days after the transfer; the length of the embryos was measured ultrasonographically on days 12, 14, 16, 18, 20, 25 and 30 after the embryo transfer. One hundred and fifteen of 200 flushes provided embryos, 12 being degenerate and 103 being viable embryos. From the 103 embryo transfers c...
Embryo recovery rate in a mare affected by Cushing’s syndrome.
Veterinary research communications    October 11, 2003   Volume 27 Suppl 1 619-621 doi: 10.1023/b:verc.0000014231.45688.ac
Panzani D, Vannozzi I, Sgorbini M, Corazza M, Rota A, Pacini M.No abstract available
Successful non-surgical transfer of horse embryos to mule recipients.
Reproduction in domestic animals = Zuchthygiene    September 3, 2003   Volume 38, Issue 5 380-385 doi: 10.1046/j.1439-0531.2003.00444.x
Camillo F, Vannozzi I, Rota A, Di Luzio B, Romagnoli S, Aria G, Allen WR.Mules, hybrids resulting from the mating of a horse mare (Equus caballus, 2n = 64) to a Jack donkey (E. asinus, 2n = 62), are generally infertile. Five horse embryos were transferred non-surgically to two cyclic and one acyclic recipient mules. In the mares and cycling mules, oestrus and ovulation were induced with, respectively, d-cloprostenol and human chorionic gonadotrophin (hCG). The acyclic mule, on the other hand, received oestradiol benzoate when the embryo donor was showing oestrus and progesterone after the donor had ovulated and until pregnancy diagnosis. Non-surgical embryo collect...
Activation of equine nuclear transfer oocytes: methods and timing of treatment in relation to nuclear remodeling.
Biology of reproduction    September 3, 2003   Volume 70, Issue 1 46-53 doi: 10.1095/biolreprod.103.018200
Choi YH, Love LB, Westhusin ME, Hinrichs K.Early development of embryos produced by transfer of equine nuclei to bovine cytoplasts is superior to that of intraspecies equine nuclear transfer embryos. This may be related to differences in chromatin remodeling or efficiency of activation between the two oocyte types. The pattern of donor nucleus remodeling was examined in equine-equine and equine-bovine reconstructed oocytes. Chromosome condensation occurred in equine cytoplasts by 2 h but was not seen in bovine cytoplasts until 4 h. We investigated the effect of activation of equine-equine reconstructed oocytes at <30 min or at 2 h a...
Cytoskeleton and chromatin reorganization in horse oocytes following intracytoplasmic sperm injection: patterns associated with normal and defective fertilization.
Biology of reproduction    March 19, 2003   Volume 69, Issue 1 186-194 doi: 10.1095/biolreprod.102.012823
Tremoleda JL, Van Haeften T, Stout TA, Colenbrander B, Bevers MM.Intracytoplasmic sperm injection (ICSI) is the method of choice for fertilizing horse oocytes in vitro. Nevertheless, for reasons that are not yet clear, embryo development rates are low. The aims of this study were to examine cytoskeletal and chromatin reorganization in horse oocytes fertilized by ICSI or activated parthenogenetically. Additional oocytes were injected with a sperm labeled with a mitochondrion-specific vital dye to help identify the contribution of the sperm to zygotic structures, in particular the centrosome. Oocytes were fixed at set intervals after sperm injection and exami...
In vitro and in vivo comparison of Ham’s F-10, Emcare holding solution and ViGro holding plus for the cooled storage of equine embryos.
Theriogenology    February 1, 2003   Volume 59, Issue 7 1615-1625 doi: 10.1016/s0093-691x(02)01210-4
Moussa M, Duchamp G, Mahla R, Bruyas JF, Daels PF.Equine embryos have been successfully transferred after 24h cooled storage in Ham's F-10. The aim of this study was to compare the viability of equine embryos in vitro and in vivo after 6 and 24h cooled storage using three media and to examine the relationship between embryo size and viability after 24h cooled storage. In Experiment 1, the viability of embryos was evaluated using DAPI-staining after 0, 6 or 24h in Ham's F-10, 24h in Emcare embryo holding solution (EHS) or 24h in ViGro holding plus (VHP) (n=10/group). The mean number of dead cells was similar for embryos stored in Ham's F-10, E...
Pregnancies attained after collection and transfer of oocytes from ovaries of five euthanatized mares.
Journal of the American Veterinary Medical Association    January 14, 2003   Volume 222, Issue 1 60-36 doi: 10.2460/javma.2003.222.60
Carnevale EM, Maclellan LJ, Coutinho da Silva MA, Squires EL.After euthanasia, ovaries were removed from 5 horses and shipped to a laboratory where 46 oocytes were collected. The oocytes were cultured for 24 to 30 hours, and 36 oocytes were transferred to 10 recipient mares via flank laparotomies. Recipient mares were inseminated with semen from various stallions. Sixteen days after transfer, 4 of the recipients were pregnant with at least 1 embryonic vesicle. Embryonic death occurred in 3 recipients, whereas a healthy live foal was born from 1 recipient. Ovaries from valuable mares can be a source of viable oocytes after death of the mare. For shipping...
The effect of co-culture on the development of in vitro matured equine oocytes after intracytoplastic sperm injection.
Equine veterinary journal    November 29, 2002   Volume 34, Issue 7 673-678 doi: 10.2746/042516402776250315
Rosati I, Berlinguer F, Bogliolo L, Leoni G, Ledda S, Naitana S.It is clear that, in the horse, there are many weak links in the process of in vitro embryo production; an optimal culture system for equine oocytes does not exist, and related data are conflicting. Therefore, the ability of 3 different culture systems to support embryonic development of ICSI horse oocytes was examined. Oocytes (n = 261) suitable for culture were collected from 55 ovaries and divided, according to cumulus morphology, into 2 categories: expanded cumulus and compacted cumulus. Oocytes with expanded and compacted cumulus were cultured for in vitro maturation in TCM 199 + 10% FCS ...
Postnatal cardiovascular function after manipulation of fetal growth by embryo transfer in the horse.
The Journal of physiology    November 15, 2002   Volume 547, Issue Pt 1 67-76 doi: 10.1113/jphysiol.2002.027409
Giussani DA, Forhead AJ, Gardner DS, Fletcher AJ, Allen WR, Fowden AL.This study used between-breed embryo transfer in the horse to investigate the effects of maternal size and uterine capacity on fetal growth and postnatal cardiovascular and neuroendocrine functions. Equine embryos were transferred to establish eight Thoroughbred-in-Thoroughbred (TinT), seven Pony-in-Pony (PinP), five Thoroughbred-in-Pony (TinP) and eight Pony-in-Thoroughbred (PinT), pregnancies. Maternal and foal weights and placental microscopic area were measured at birth. At 6 days of postnatal life, arterial blood pressure and heart rate were monitored and blood samples were taken for horm...
Pregnancies from vitrified equine oocytes collected from super-stimulated and non-stimulated mares.
Theriogenology    September 6, 2002   Volume 58, Issue 5 911-919 doi: 10.1016/s0093-691x(02)00920-2
Maclellan LJ, Carnevale EM, Coutinho da Silva MA, Scoggin CF, Bruemmer JE, Squires EL.The objectives were to compare embryo development rates after transfer into inseminated recipients, vitrified thawed oocytes collected from super-stimulated versus non-stimulated mares. In vivo matured oocytes were collected by transvaginal, ultrasound guided follicular aspiration from super-stimulated and non-stimulated mares 24-26 h after administration of hCG. Oocytes were cultured for 2-4 h prior to vitrification. Cryoprotectants were loaded in three steps before oocytes were placed onto a 0.5-0.7 mm diameter nylon cryoloop and plunged directly into liquid nitrogen. Oocytes were thawed and...
Production of nuclear transfer horse embryos by Piezo-driven injection of somatic cell nuclei and activation with stallion sperm cytosolic extract.
Biology of reproduction    July 24, 2002   Volume 67, Issue 2 561-567 doi: 10.1095/biolreprod67.2.561
Choi YH, Love CC, Chung YG, Varner DD, Westhusin ME, Burghardt RC, Hinrichs K.We investigated the use of direct nuclear injection using the Piezo drill and activation by injection of stallion sperm cytosolic extract for production of cloned equine embryos. When metaphase II horse oocytes were injected with either of two dosages of sperm extract and cultured 20 h, similar activation rates (88% vs. 90%) and cleavage rates (49% vs. 46%) were obtained. The successful reconstruction rate of horse oocytes with horse somatic cell donor nuclei after direct injection using the Piezo drill was 82%. Four dosages of sperm extract (containing 59, 176, 293, or 1375 microg/ml protein)...
Effect of time of oocyte collection and site of insemination on oocyte transfer in mares.
Journal of animal science    May 22, 2002   Volume 80, Issue 5 1275-1279 doi: 10.2527/2002.8051275x
Coutinho da Silva MA, Carnevale EM, Maclellan LJ, Seidel GE, Squires EL.The objective of the study was to compare embryo development rates after transfer of oocytes collected 22 or 33 h after hCG injection into recipients inseminated within the uterus or the oviduct. Oocytes were collected at approximately 22 or 33 h after hCG injections and incubated for approximately 16 or 1.5 h, respectively, before transfer. Intrauterine inseminations using 1 x 10(9) progressively motile sperm were done approximately 12 h before and 2 h after transfer. For intraoviductal inseminations (gamete intrafallopian transfer [GIFT]), semen was centrifuged through a Percoll gradient, an...
[Successful direct transfer of a deep frozen-thawed equine embryo].
DTW. Deutsche tierarztliche Wochenschrift    March 14, 2002   Volume 109, Issue 2 61-62 
Ulrich P, Nowshari MA.Embryos were flushed on day 7 after ovulation from two mares, and frozen using a conventional slow freezing procedure in phosphate buffered (PBS) saline supplemented with 10% FCS, 1.5 mol/L ethylene glycol and 0.25 mol/L sucrose. One of the two embryos was thawed after 10 months of storage in liquid nitrogen and transferred directly (without dilution of the cryoprotectant and quality examination) to a synchronized recipient. This transfer resulted in the birth of a live female foal. To our knowledge, this is the first live foal born after direct transfer of a frozen-thawed equine embryo.
Influence of maternal size on placental, fetal and postnatal growth in the horse. I. Development in utero.
Reproduction (Cambridge, England)    March 8, 2002   Volume 123, Issue 3 445-453 
Allen WR, Wilsher S, Turnbull C, Stewart F, Ousey J, Rossdale PD, Fowden AL.The interacting influences of maternal size and fetal genotype on placental and fetal development in the mare were assessed by comparing conventional within-breed Thoroughbred (Tb-in-Tb, n = 7) and Pony (P-in-P, n = 7) control pregnancies established by artificial insemination (AI) with between-breed (Tb-in-P, n = 8; deprived in utero condition and P-in-Tb, n = 7; luxurious in utero condition) experimental pregnancies established by embryo transfer. All foals were born spontaneously and the mean (+/- SEM) duration of gestation in the two groups of control mares was significantly different (P <...
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...
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