Analyze Diet

Topic:Embryo

Equine embryo research focuses on the early developmental stages of horses, encompassing the formation, growth, and differentiation of the embryo. This area of study is significant for understanding reproductive biology, improving breeding programs, and advancing assisted reproductive technologies in equines. Key aspects include the processes of fertilization, embryonic development, and implantation. Researchers investigate factors influencing embryonic viability, such as genetic and environmental influences, to enhance reproductive success rates. This page aggregates peer-reviewed research studies and scholarly articles that explore the biological mechanisms, technological advancements, and applied methodologies related to equine embryos.
Large equine blastocysts are damaged by vitrification procedures.
Reproduction, fertility, and development    January 1, 1995   Volume 7, Issue 1 113-117 doi: 10.1071/rd9950113
Hochi S, Fujimoto T, Oguri N.Viability following vitrification of equine blastocysts with different sizes was investigated in vitro. Twenty-four blastocysts were classified into three groups according to their diameters ( 300 microns; n = 8 each). The solution used for vitrification was defined as EFS and contained 40% ethylene glycol, 18% Ficoll and 0.3 M sucrose in modified-phosphate-buffered saline (m-PBS). During pretreatment with 20% ethylene glycol in m-PBS for 20 min, the larger blastocysts responded to the osmotic pressure caused by 20% ethylene glycol more slowly than the smaller blastocysts. Single blastocysts w...
Effect of glucose in the culture medium on development of horse oocytes matured and microfertilized in vitro.
Reproduction, fertility, and development    January 1, 1995   Volume 7, Issue 5 1067-1071 doi: 10.1071/rd9951067
Azuma T, Choi YH, Hochi S, Oguri N.The development of in-vitro matured and microfertilized horse oocytes was examined in vitro. Fertilized oocytes were produced by 20-h insemination of in-vitro matured and partially zona-removed oocytes with frozen spermatozoa that had been treated with caffeine/calcium ionophore A23187 (fertilization rate 34.2%, monospermy rate 76.9%). Embryonic development was assessed by the number of nuclei stained with Giemsa solution. In Experiment 1, a continuous 8-day culture of the microfertilized oocytes in TCM199 or modified synthetic oviduct fluid (m-SOF) supplemented with 10% fetal bovine serum or ...
[Embryo transfer in horses–current status and future perspectives].
Tierarztliche Praxis    December 1, 1994   Volume 22, Issue 6 558-566 
Braun J.Although foals born after embryo transfer are eligible for registration in the majority of horse breeds, application of embryo transfer is still rare. This is mainly due to the lack of a possibility for superovulation. Uterine stage embryos can be recovered by a non-surgical flushing technique. Transfer can be accomplished by non-surgical as well as surgical methods. In contrast to the situation in cattle, most related technologies are scarcely available. Methods of cryopreservation as well as bisection of embryos are hampered by the fact that suitable embryos (morula) can be collected from th...
In vitro development of day 2 embryos obtained from young, fertile mares and aged, subfertile mares.
Journal of reproduction and fertility    November 1, 1994   Volume 102, Issue 2 371-378 doi: 10.1530/jrf.0.1020371
Brinsko SP, Ball BA, Miller PG, Thomas PG, Ellington JE.This study was designed to investigate the development of day 2 embryos obtained from young and aged mares, co-cultured with oviductal epithelial cells obtained from mares in each age group in a 2 x 2 crossover design. Young, fertile mares (n = 19; 2-7 years of age) and aged, subfertile, mares (n = 16; 17-24 years of age) were used as embryo and oviductal epithelial cell donors. Embryos (n = 37) were collected from the oviducts 2 days after ovulation and were paired (embryos obtained from young mares with embryos obtained from aged mares) so that eight pairs were co-cultured with young mare ov...
Induction of superovulation in DD mice at different stages of the oestrous cycle.
Journal of reproduction and fertility    November 1, 1994   Volume 102, Issue 2 263-267 doi: 10.1530/jrf.0.1020263
Redina OE, Amstislavsky SYa , Maksimovsky LF.This study examined the developmental capacity of oocytes in DD mice after they had been injected with pregnant mares' serum gonadotrophin at different stages of the oestrous cycle. The superovulation of mature DD mice at pro-oestrus, oestrus and metoestrus resulted in a large yield of viable embryos. The proportion of abnormal embryos was highest after injection of pregnant mares' serum gonadotrophin at dioestrus. The pool of viable oocytes was most synchronized with normal development after the hormone was injected at oestrus. The results demonstrate that oocytes of different morphology coul...
In vitro fertilization rate of horse oocytes with partially removed zonae.
Theriogenology    October 1, 1994   Volume 42, Issue 5 795-802 doi: 10.1016/0093-691x(94)90448-r
Choi YH, Okada Y, Hochi S, Braun J, Sato K, Oguri N.Frozen-thawed ejaculated stallion spermatozoa were preincubated for 3 h in BO medium containing 5 mM caffeine and then treated with 0.1 micro M calcium ionophore A23187 for 60 sec. Aliquots of the sperm suspension (final concentration 1-2 x 10(7)/ml) were added to the oocytes which had been matured in vitro for 32 h. In Experiment 1, there were 3 groups of oocytes; cumulus intact, denuded zona-intact, and zona-free. Cumulus cells were removed with 0.5% hyaluronidase and the zona pellucida with 0.1% protease. The oocytes were fixed 20 h after insemination with acetic acid:ethanol (1:3) and stai...
In vitro viability of cryopreserved equine embryos following different freezing protocols.
Canadian journal of veterinary research = Revue canadienne de recherche veterinaire    October 1, 1994   Volume 58, Issue 4 235-241 
Poitras P, Guay P, Vaillancourt D, Zidane N, Bigras-Poulin M.The main objective of this study was to evaluate two freezing protocols and the effect of agar embedding on survival of day 6.5 equine embryos. A total of 133 embryos were used, in one group (n = 51), embryos were first embedded in agar before the freezing protocol was started. A freezing protocol to -30 degrees C or -33 degrees C was used before plunging embryos into liquid nitrogen (LN2). The embryos were thawed in water at 37 degrees C, evaluated and placed in culture. After 24 h culture, the embryos were evaluated for their morphology and development. No differences were observed between e...
The equine embryonic capsule practical implications of recent research.
Equine veterinary journal    May 1, 1994   Volume 26, Issue 3 184-186 doi: 10.1111/j.2042-3306.1994.tb04366.x
Oriol JG.In most domestic animals, the zona pellucida is the outermost extracellular layer that covers the blastocyst before implantation. However, in the horse, an acellular membrane, the capsule, replaces the zona pellucida and envelops the developing conceptus during the 2nd and 3rd weeks of gestation. Although this structure was first described by Bonnet in 1889, it received little attention until the 1970s when its rediscovery by Marrable and Flood (1975) led to a series of reports (see review by Betteridge 1989). Nevertheless, until recently the structure, origin, and function of the capsule have...
Binding of epidermal growth factor and transforming growth factor-alpha in mammalian preimplantation embryos.
Theriogenology    January 1, 1994   Volume 41, Issue 4 879-887 doi: 10.1016/0093-691x(94)90503-b
Fischer B, Rose-Hellekant TA, Sheffield LG, Bertics PJ, Bavister BD.Preimplantation embryos of the pig (Days 11 to 15), cow (Days 14 to 16), sheep (Day 14) and pony (Day 16) bind epidermal growth factor (EGF) specifically. Binding was not detected in embryos of the rabbit at Day 5 or 6 or the hamster at Day 3. Transforming growth factor-alpha displaced [(125)I] EGF in pig, cow and pony embryos almost as much as unlabeled EGF. The binding affinities of EGF ranged from 12 to 233 pM in pig and cow embryos. The range of species and binding features indicate that the EGF family may play a significant role in mammalian preimplantation development.
Culture of equine embryos in media containing egg yolk, mare’s milk and saline: Preliminary results.
Theriogenology    January 1, 1994   Volume 41, Issue 6 1201-1206 doi: 10.1016/0093-691x(94)90476-y
Lebedev SG, Lebedeva LF.A medium containing egg yolk, mare's milk and/or modified PBS was used to culture Day-8 to 8.5 equine blastocysts. Twenty-one variants of the medium containing different concentrations of the 3 components were prepared. Embryos were recovered nonsurgically and placed into the media at 37 degrees C for 24 h. A total of 45 embryos was cultured; of these 7 died in culture and 13 showed inadequate development at the onset, while 25 continued to grow in the media. It was established that embryos grew best in media containing 20 to 60% yolk, 20 to 60% mare's milk and/or 20 to 60% PBS. It was found e...
Fertilization rates in superovulated and spontaneously ovulating mares.
Theriogenology    January 1, 1994   Volume 41, Issue 7 1411-1423 doi: 10.1016/0093-691x(94)90192-l
Dippert KD, Jasko DJ, Seidel GE, Squires EL.Embryo recovery per ovulation has been shown to be lower in superovulated mares than in untreated controls. The objectives of this study were to 1) determine whether follicles stimulated with superovulatory treatment ovulate or luteinize without ovulation, 2) determine fertilization rates of oocytes in oviducts of superovulated and control mares, and 3) evaluate viability of early stage embryos from superovulated and control mares when cultured in equine oviductal cell-conditioned medium. Cyclic mares were randomly assigned to 1 of 2 groups (n=14 per group) on the day of ovulation (Day 0): Gro...
Developmentally regulated changes in the glycoproteins of the equine embryonic capsule.
Journal of reproduction and fertility    November 1, 1993   Volume 99, Issue 2 653-664 doi: 10.1530/jrf.0.0990653
Oriol JG, Sharom FJ, Betteridge KJ.The embryonic capsule, which covers the equine blastocyst after it loses its zona pellucida, is composed of mucin-like glycoproteins. In the present study, we investigated both macroscopic and molecular changes in the capsule during development. The weight of the capsule increased from day 11-12 of pregnancy and reached a maximum at about day 18, coinciding with the time during which the conceptus migrates extensively throughout the uterus. The sialic acid content of the capsule declined markedly from about day 16, the time of conceptus 'fixation' in the uterus, which suggests a unique develop...
Quantitative analysis of morphological modifications of day 6.5 horse embryos after cryopreservation: differential effects on inner cell mass and trophoblast cells.
Journal of reproduction and fertility    September 1, 1993   Volume 99, Issue 1 15-23 doi: 10.1530/jrf.0.0990015
Bruyas JF, Bézard J, Lagneaux D, Palmer E.Sixteen embryos were recovered nonsurgically at day 6.5 after induced ovulation from Welsh pony mares and were evaluated for cellular changes that occur because of exposure to the cryoprotectant with or without the freeze and thaw process. Day 6.5 horse embryos were either (i) frozen and thawed using glycerol as cryoprotectant (n = 6), (ii) given only the glycerol treatment (n = 5), or (iii) washed in phosphate-buffered saline (PBS) the same number of times as in the glycerol treatment (n = 5). After treatments, embryos were incubated in Minimum Essential Medium (MEM), supplemented with BSA, g...
Uterine transport of prostaglandin E(2)-releasing simulated embryonic vesicles in mares.
Theriogenology    July 1, 1993   Volume 40, Issue 1 13-20 doi: 10.1016/0093-691x(93)90337-5
Vanderwall DK, Woods GL, Weber JA, Lichtenwalner AB.Transrectal ultrasonography was used to test the hypothesis that prostaglandin E(2) (PGE(2)) would increase the uterine transport of simulated embryonic vesicles in mares. Uterine transport of PGE(2)-releasing (PGE) vesicles, vehicle-releasing (sham) vesicles, and equine embryos was contrasted on Day 12 or Day 13 post ovulation. In Experiment 1, there was no difference (P>0.10) in transport of PGE vesicles, sham vesicles, Day-12 embryos, and Day-12 embryos after cervical manipulation (n = 3 per group). In Experiments 2 and 3, respectively, transport of PGE and sham vesicles was contrasted with...
Development to blastocysts of one- to two-cell equine embryos after coculture with uterine tubal epithelial cells.
American journal of veterinary research    July 1, 1993   Volume 54, Issue 7 1139-1144 
Ball BA, Brinsko SP, Thomas PG, Miller PG, Ellington JE.Development of 1- to 2-cell in vivo fertilized equine embryos cultured with or without uterine tubal epithelial cells (UTEC) was studied. One- to 2-cell embryos (n = 26) were collected surgically from the uterine tubes of pony mares 1 day after ovulation. Four- to 8-cell embryos (n = 9) were collected 2 days after ovulation. Presumptive zygotes and 2-cell embryos were cultured with (n = 17) or without (n = 9) UTEC, and all 4- to 8-cell embryos were cocultured with UTEC as positive controls. Uterine tubal epithelial cells were used as cell suspensions within 2 weeks after initiation of cultures...
Mucin-like glycoproteins in the equine embryonic capsule.
Molecular reproduction and development    March 1, 1993   Volume 34, Issue 3 255-265 doi: 10.1002/mrd.1080340305
Oriol JG, Betteridge KJ, Clarke AJ, Sharom FJ.The equine embryonic capsule replaces the zona pellucida and envelopes the conceptus during the second and third weeks of pregnancy. Although this capsule was described more than 100 years ago, its molecular structure has not been characterized. Here we present evidence that the glycoprotein(s) of the equine capsule resembles those of the mucin glycoprotein family. The resistance of the capsule to chemical and enzymatic solubilization was confirmed, and, as in mucins, protein constituted only 35-40% of its total dry mass. Determination of the sugar composition of the capsule using colorimetric...
[Prenatal development of the horse ovary].
Anatomia, histologia, embryologia    December 1, 1992   Volume 21, Issue 4 306-313 doi: 10.1111/j.1439-0264.1992.tb00462.x
Knospe C, Budras KD.To answer the many open questions concerning the development of the horse's ovary, first the prenatal development was investigated. It resulted that follicles derive from the germinal epithelium and its cords, whereas the Leydig cells and the rete blastema originate from the mesonephros. In the second third of pregnancy the Leydig cells undergo an enormous proliferation, in the last third they degenerate. However this degeneration is not connected with the postnatal development of the ovulation groove.
Influence of exogenous progesterone on early embryonic development in the mare.
Theriogenology    December 1, 1992   Volume 38, Issue 6 1055-1063 doi: 10.1016/0093-691x(92)90119-c
Ball BA, Miller PG, Daels PF.The influence of exogenous progesterone on the development of equine oviductal embryos was determined based upon the recovery of Day-7 uterine blastocysts from treated mares (n=13) that were given 450 mg progesterone daily between Days 0 and 6 and from untreated control mares (n=13). Daily administration of 450 mg progesterone in oil significantly (P<0.02) increased serum progesterone concentrations in the treated mares. There was no significant difference in the recovery rate of Day-7 embryos between treated and control mares (8/13 versus 6/13, respectively). Embryonic development, assesse...
Initiation of superovulation in mares 5 or 12 days after ovulation using equine pituitary extract with or without GnRH analogue.
Theriogenology    October 1, 1992   Volume 38, Issue 4 695-710 doi: 10.1016/0093-691x(92)90032-m
Dippert KD, Hofferer S, Palmer E, Jasko DJ, Squires EL.Cyclic mares were assigned to 1 of 3 treatments (n=15 per group): Group 1 received equine pituitary extract (EPE; 25 mg, i.m.) on Day 5 after ovulation; Group 2 received EPE on Day 12 after ovulation; while Group 3 received 3.3 mg of GnRH analogue (buserelin implant) on the day of ovulation and 25 mg, i.m. EPE on Day 12. Mares in each group were given 10 mg PGF2alpha on the first and second day of EPE treatment. The EPE treatment was continued daily until the first spontaneous ovulation, at which time 3,300 IU of human chorionic gonadotropin (hCG) were given to induce further ovulations. Mares...
[Early sonographic diagnosis of twin pregnancy in mares and its reduction to a single pregnancy].
Tierarztliche Praxis    August 1, 1992   Volume 20, Issue 4 399-404 
Kudlac E, Grygar J.The frequency of double ovulation and the chances of twin pregnancy in the mare are presented with reference to the relevant literature. A novel manual technique for reducing the embryo number from two to one is introduced and illustrated by ultrasonographic images.
Role of the embryonic vesicle and progesterone in embryonic loss in mares.
Journal of reproduction and fertility    July 1, 1992   Volume 95, Issue 2 339-347 doi: 10.1530/jrf.0.0950339
Bergfelt DR, Woods JA, Ginther OJ.Characteristics of spontaneous embryonic loss in 21 mares were compared with those of 52 contemporary mares that maintained pregnancy. Embryonic losses were, in retrospect, grouped according to day of loss and length of the interovulatory interval, respectively, as follows: group 1, less than or equal to day 20 and less than or equal to 30 days (n = 10); group 2, less than or equal to day 20 and greater than 30 days (n = 3); and group 3, greater than day 20 and greater than 30 days (n = 8); ovulation was day 0. Mean diameter of the embryonic vesicle in group 1 was smaller (P less than 0.05) on...
Relationships of age to uterine function and reproductive efficiency in mares.
Theriogenology    May 1, 1992   Volume 37, Issue 5 1101-1115 doi: 10.1016/0093-691x(92)90108-4
Carnevale EM, Ginther OJ.The uterine function and reproductive efficiency of 31 nonlactating pony mares were compared for two age groups: young (5 to 7 years, n=9) and old (>/=15 years, n=22). For pregnant mares, differences between age groups were not significant for the diameter of the largest follicle, cross-sectional area of the corpus luteum, growth profile of the embryonic vesicle or embryo mobility characteristics. Uterine contractility scores were lower (P<0.05), day of fixation of the embryonic vesicle was later (P<0.05), and uterine tone tended (P<0.10) to be lower in the old than the young mares...
Superovulation of cattle with equine pituitary extract and porcine ESH.
Theriogenology    May 1, 1992   Volume 37, Issue 5 1091-1099 doi: 10.1016/0093-691x(92)90107-3
Staigmiller RB, Bellows RA, Anderson GB, Seidel GE, Foote WD, Menino AR, Wright RW.Superovulation has been practiced in cattle for more than 50 years but the results have been highly variable. Scientists at six locations compared a horse pituitary extract (HAP) with a single batch of porcine FSH (pFSH) to determine the efficacy of these hormones to induce superovulation and to test for variability in the superovulatory response. Acetone-dried equine pituitaries were suspended in 40% ethanol containing 6% ammonium acetate, and the supernatant was mixed with 2.5 volumes of cold ethanol. The resulting precipitate was washed with cold ether and dried. Total doses of 18 mg of HAP...
Prostaglandin E2 secretion by day-6 to day-9 equine embryos.
Prostaglandins    January 1, 1992   Volume 43, Issue 1 55-59 doi: 10.1016/0090-6980(92)90064-z
Weber JA, Woods GL, Freeman DA, Vanderwall DK.Prostaglandin E2 (PGE2) secreted by Day-6, Day-7, Day-8 and Day-9 equine embryos (ovulation = Day 0) during in vitro incubation was measured by radioimmunoassay. Embryonic PGE2 secretion (ng/embryo/24 hr) was detectable on Day 6 (0.27 +/- 0.39), tended to increase (P less than 0.1) on Day 7 (0.57 +/- 0.88), and increased significantly (P less than 0.05) on Day 8 (2.23 +/- 0.86) and Day 9 (4.13 +/- 0.71). Embryo diameter at the start of the incubation period was linearly correlated (P less than 0.01) to embryonic PGE2 secretion.
Prostaglandin E2-specific binding to the equine oviduct.
Prostaglandins    January 1, 1992   Volume 43, Issue 1 61-65 doi: 10.1016/0090-6980(92)90065-2
Weber JA, Woods GL, Freeman DA, Vanderwall DK.Prostaglandin E2 (PGE2) bound specifically (P less than 0.001) to ampullary and isthmic tissue on Day 2 and Day 5 after ovulation. No significant differences (P greater than 0.8) were detected between Day 2 and Day 5 in the specific binding of ampullary or isthmic tissue. Significantly more (P less than 0.05) PGE2 bound specifically to ampullary versus isthmic tissue on both days. Detection of PGE2-specific binding in the oviductal isthmus on Day 2 and Day 5 indicates that the oviduct is responsive to PGE2 when it is capable of transporting equine embryos.
Quantifying the occurrence of early embryonic mortality on three equine breeding farms.
The Canadian veterinary journal = La revue veterinaire canadienne    November 1, 1991   Volume 32, Issue 11 665-672 
Meyers PJ, Bonnett BN, McKee SL.This prospective field study was designed to describe the incidence of early embryonic mortality (EEM) and factors associated with the cause of EEM on three equine breeding farms in Ontario during the 1989 breeding season. Early embryonic mortality was defined as the loss of a single embryo during the first 40 days of pregnancy (day 0 = day of ovulation or last breeding). Pregnancy diagnoses and subsequent embryonic losses were observed by serial trans-rectal ultrasonography between days 12-20 (PD1) and 21-30 (PD2), and by trans-rectal ultrasonography or palpation per rectum between days 31-40...
Time of embryo transport through the mare oviduct.
Theriogenology    November 1, 1991   Volume 36, Issue 5 823-830 doi: 10.1016/0093-691x(91)90348-h
Freeman DA, Weber JA, Geary RT, Woods GL.The objectives of this study were 1) to determine the time of embryo transport through the mare oviduct, 2) to determine whether equine embryos increase in diameter prior to the time of oviductal transport, and 3) to assess the stage of equine embryonic development at the time of oviductal transport. The time of oviductal transport (interval from ovulation to uterine entry) was estimated by collecting embryos from the mare oviduct or uterus at 2-hour intervals from 120 to 168 h postovulation. The time of oviductal transport was 130 to 142 h, since 9 9 embryos were located in the oviduct from 1...
Co-culture of day-5 to day-7 equine embryos in medium with oviductal tissue.
Theriogenology    November 1, 1991   Volume 36, Issue 5 815-822 doi: 10.1016/0093-691x(91)90347-g
Freeman DA, Butler JE, Weber JA, Geary RT, Woods GL.Oviductal and uterine embryos were collected from mares at 5 to 7 days following ovulation 1) to evaluate the effects of oviductal tissue explants on in vitro growth and development of equine embryos and 2) to study the morphologic development of equine embryos in culture. Embryos were incubated for 5 days in a medium (control group) or in medium supplemented with oviductal tissue explants (co-culture group). Embryos were evaluated and the media changed daily. Following 5 days in culture, 10 10 (100%) control embryos and 27 29 (93%) co-cultured embryos had doubled in diameter. All embryos that...
Prostaglandin E2 secretion by oviductal transport-stage equine embryos.
Biology of reproduction    October 1, 1991   Volume 45, Issue 4 540-543 doi: 10.1095/biolreprod45.4.540
Weber JA, Freeman DA, Vanderwall DK, Woods GL.This study was conducted to identify embryonic products whose secretion was temporally associated with the oviductal transport period of the mare. Chemicals secreted by oviductal-transport-stage equine embryos were identified by incubating Day 6 or Day 7 early uterine embryos with 35S-methionine/cysteine, 3H-progesterone, or 3H-arachidonic acid for 24 h, and subsequently identifying radioactively labeled proteins (SDS-PAGE; n = 3 embryos), steroids (HPLC; n = 3 embryos), or prostaglandins (HPLC; n = 3 embryos) in the culture medium. Early uterine embryos secreted 116.1 +/- 45.5 pg of prostagla...
Prostaglandin E2 hastens oviductal transport of equine embryos.
Biology of reproduction    October 1, 1991   Volume 45, Issue 4 544-546 doi: 10.1095/biolreprod45.4.544
Weber JA, Freeman DA, Vanderwall DK, Woods GL.The hypothesis that treatment of pregnant mares with prostaglandin E2 (PGE2) hastens the oviductal transport of equine embryos was tested by treating bred mares with PGE2 on Day 3 after ovulation and subsequently measuring the rate of hastened oviductal transport (estimated by the uterine embryo recovery rate on Day 4 after ovulation). In a preliminary, noncontrolled experiment, oviductal transport was apparently not hastened after intramuscular, intrauterine, or intraperitoneal PGE2 administration to bred mares (0/6, 0/3, and 0/3 mares, respectively). Oviductal transport appeared to be hasten...
1 18 19 20 21 22 24