Reproductive Parameters of Mangalarga Marchador Mares in a Commercial Embryo Transfer Programme (original) (raw)
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Animal Reproduction Science, 2015
Advanced maternal age is an important predisposing factor on the reduction of reproductive efficiency. The aim of this study was to evaluate the effect of donor's age on several reproductive parameters in a commercial equine embryo transfer program. Donors were classified into 3 age groups: Group 1 = fillies (3 and 4 years old), Group 2 = middle age mares (aged 5-10) and Group 3 = old mares (aged 13-25). Embryo recovery, multiple ovulation and pregnancy rates and interovulatory intervals were compared amongst age groups. Group 1 (171/244, 70.1%) and Group 2 (774/1081, 71.6%) had a higher (P < 0.005) embryo recovery rate than Group 3 (385/701, 54.9%). Groups 2 and 3 were 2.5 and 3.4 times more likely to have multiple ovulations than Group 1 (P < 0.05), respectively. The effect of age group on pregnancy rate was not significant (P > 0.05). The interovulatory intervals length was influenced by individual mare (P < 0.001), age (P < 0.04), Day of flushing (P = 0.009) and by month (P < 0.012). The overall mean interovulatory interval of Group 1 (16.4 ± 0.17 days) and Group 2 (16.6 ± 0.12 days) was not different (P > 0.05), but was shorter than the one of Group 3 (17.4 ± 0.15 days; P < 0.04). The embryo recovery rate of flushings from Groups 1 and 2 was influenced by the length of the previous interovulatory interval (P = 0.03).
Factors affecting the success of oocyte transfer in a clinical program for subfertile mares
Theriogenology, 2005
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 AE 0.4 yr of age (mean AE 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 AE 0.1 h after administration of hCG to estrous donors and cultured 16.4 AE 0.2 h prior to transfer into recipients' oviducts. At 16 and 50 d after transfer, pregnancies were detected in 201 of 504 (40%) and 159 of 504 (32%) of recipients, respectively, with an embryo-loss rate of 21% (42/201). Pregnancy rates were similar (P > 0.05) for cyclic and noncyclic recipients and for recipients inseminated with cooled, fresh or frozen semen. One or more recipients were detected pregnant at 16 and 50 d, respectively, for 80% (69/86) and 71% (61/86) of donors. More donors <20 than !20 yr (mean ages AE S.E.M. of 15.5 AE 0.4 and 23.0 AE 0.3 yr, respectively) tended (P = 0.1) to have one or more pregnant recipients at 50 d (36/45, 80%; 28/45, 62%, respectively). Results of the program confirm that pregnancies can consistently be obtained from older, subfertile mares using oocyte transfer. #
Reproduction, 2004
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 inseminated with semen from two different stallions at 15 h before and 2.5 h after oocyte transfer. Sixteen days after transfer, embryos were recovered from uteri and submitted for parentage testing. The percentage of oocytes resulting in embryonic vesicles was nearly identical (P > 0.05) for transferred oocytes (32/44, 73%) versus ovulated oocytes of recipients (9/13, 69%). More (P < 0.01) oocytes were fertilized by sperm inseminated before (35/38, 92%) versus after (3/38, 8%) oocyte transfer. Tissue culture medium (TCM)-199 was superior to equine maturation medium I (EMMI; a SOF-based medium) for culturing oocytes (P < 0.05), although addition of hormones and growth factors during culture did not improve (P > 0.05) development of embryos.
Equine Veterinary Journal, 2017
Background: Previous surveys reported a positive association between the length of the follicular phase and subsequent fertility in embryo transfer donor and Thoroughbred mares. However, it is unclear whether a longer oestrus positively influences fertilisation and oviductal development (oocyte quality, oviductal environment), or uterine receptivity and survival of the embryo in the uterus.
Animal reproduction science, 2018
The objective of this study was to evaluate the environmental effects on embryo recovery rate and pregnancy rate of Mangalarga Marchador mares. The reproductive characteristics of donor and recipient mares were evaluated during five years in Brazilian tropical environment. The mares were used throughout the year and seasons were classified as: October to April (breeding season - BS); May (autumn transition out of the breeding season - ATBS); June to August (non-breeding season - nBS); and September (vernal transition into the breeding season - VTBS). Daily temperature rainfall and hours of daylight (photoperiod) were measured during all months and years of evaluation. The embryo recovery rate (ERR) and the pregnancy rate (PR) were observed and frequencies were calculated. The effect of environmental variables, day of flushing, and hormonal treatments (estradiol benzoate and progesterone) were determined for the reproductive measures using the Chi-square and Kruskal-Wallis tests. Sig...
Recovery rate and quality of embryos from mares inseminated after ovulation
Theriogenology, 1996
The aim of this study was to evaluate the quality of embryos and their recovery rate from mares inseminated at different intervals after ovulation. Finnhorse and warmblood mares were inseminated with fresh semen 8 to 16 h, 16 to 24 h, or 24 to 32 h after ovulation. Control mares were inseminated before ovulation. Sixty-seven embryo flushings were performed between Days 7 and 9 after ovulation/insemination. Thirteen mares were not flushed, but their uteri were scanned for pregnancy on Days 14 to 16. Embryo recovery rates decreased as time from ovulation to insemination increased, although embryo quality remained normal as evaluated by morphological criteria and mitotic index. However, postovulatory insemination in this trial appeared to delay embryo development, since the embryos recovered from mares inseminated after ovulation were appreciably smaller and at an earlier stage of development than control embryos recovered from mares inseminated prior to ovulation. Part of this delay in embryo development in the postovulation group could be due to the time needed for sperm capacitation. In addition, as the time from ovulation to insemination increased, embryo development might have been further delayed by defects in the aging oocyte.
PloS one, 2024
Equine embryo transfer (EET) is a prominent technology in the equine breeding industry, and its efficacy is affected by a number of factors. The current study aimed to determine the effects of the breed of donor/recipient mares, estrus/ovulation induction treatment, cooled transportation of embryos, and synchrony between donor and recipient mares on the efficiency of the EET under subtropical conditions of Pakistan. A total of eighty-four (n = 84) Polo-playing donor mares (Argentino-polo = 41 and Anglo-Arab = 43) and seventy (n = 70) recipient mares (light breed = 26 and heavy breed = 44) were used for EET. The donor mares exhibiting natural estrus (n = 28) were detected by teaser a stallion, and corpus luteum (CL) having mares (n = 56) were treated with prostaglandin (150 μg of Cloprostenol) for estrus induction. The mares' follicular growth was monitored through ultrasonography until the dominant follicle's size reached 35 mm or more with a moderate to obvious uterine edema score. Afterward, the mares were treated either with GnRH, i.e., 50 μg of Lecirelin acetate (n = 41) or Ovusyn, i.e., 1500 IU hCG (n = 43). Insemination with chilled semen was performed 24 hours later. The embryos were collected non-surgically, 7 or 8 days after ovulation, from the donor mares. The collected embryos were transferred into the well-synchronized recipient mares as fresh (n = 44) or chilled (n = 26) embryos. The pregnancy after ET was checked through ultrasonography. Statistical analysis revealed that the embryo recovery rate (ERR) remained significantly higher (P<0.05) for the Prostaglandin (PG) treated group of donors as compared to the natural heat group of donors. The breed of donor mares, type of ovulatory treatment given, and day of embryo collection did not significantly (P>0.05) affect the ERR. There was no significant effect of the type (fresh vs chilled), classification, and stage of development of embryo on pregnancy outcomes (P>0.05). ET pregnancy rate was significantly affected by the breed of recipient mares and ovulation synchrony between donor and recipient mares (P<0.05). In conclusion, under the subtropical conditions of Pakistan, PG-based estrus induction of donor mares, breed of recipient mares, and ovulation synchrony between the donor and recipient mares had a substantial effect on the efficiency of EET.
Journal of Equine Veterinary Science, 2016
The present study aimed to evaluate pregnancy and pregnancy loss rates of recipients treated with alternative long-acting progesterone protocols, designed to synchronize acyclic and cyclic mares, regardless of their cycle phase. A total of 150 Campolina breed mares were used as recipients. Recipient mares were assigned to six different groups with 25 animals each. Groups 1 to 5 were treated with progesterone at some point. Group 1 (acyclic recipients); group 2 (cyclic estrous recipients with one !35 mm follicle); group 3 (cyclic estrous recipients with an anovulatory follicle); group 4 (early estrous cyclic recipients); group 5 (diestrous cyclic recipients), and group 6 (cyclic recipientsdcontrol). Embryos (day 8) were transferred 4 days after ovulation or 4 days after progesterone injection. Pregnant diagnosis was performed by transrectal ultrasonography 1 week after embryo transfer. Pregnant recipients were evaluated for possible losses and mares treated every 14 days with 3 g (intramuscular) of long-acting progesterone, until 120 days of pregnancy. Pregnancy at 15 days and pregnancy loss rates were recorded and statistically evaluated through multivariate regression (P < .05). Pregnancy and pregnancy loss rates were similar within groups (G1: 76%-10.5%; G2: 76%-5.9%; G3: 56%-0%; G4: 80%-10%; G5: 60.9%-0%; and G6: 60%-13.3%). In conclusion, the novel long-acting progesterone protocols proposed in this study allowed successfully the utilization of mares with asynchronous cyclic as embryo recipients, serving as an alternative specially when few recipients are available and usual synchronization is not possible.
Theriogenology, 2014
In this study, 198 donor mares of different breeds, ages and reproductive category were inseminated with fresh, cooled, frozen or frozen and cooled semen at the embryo transfer station or in private AI centers during 10 breeding seasons. The results of this activity were retrospectively analyzed by Pearson Chi-Square test and logistic regression to evaluate factors affecting multiple ovulations, embryo recovery, embryo quality and embryo diameter. Out of the 661 cycles, 937 ovulations were recorded (mean ovulations/cycle: 1.42 ± 0.58). Ovulation rate and incidence of multiple ovulations were significantly affected by age, breed and reproductive category. Uterine flushings for embryo recovery were performed between 7 and 10 days after ovulation and resulted in the recovery of 338 embryos (51.1% embryos/cycle and 36.1% embryos/ovulation, respectively). At least one embryo was recovered in 298 flushings (45.1%). The factors affecting embryo recovery were age, breed, reproductive category, type of semen, number of ovulations and location of AI. Flushing protocol and day of flushing had no effect on embryo recovery. Age, type of semen, number of ovulations and day of flushing had a significant influence on embryo diameter (N= 215). None of the factors included in the model had an effect on embryo quality distribution.