Multiple ovulation and embryo transfer is one of the reproductivetechnologies which is important to increase animal production. In this case report, four cows were selected as donors while elevencows were selected as recipients. Both donors and recipients had undergone the same procedures and steps for multiple ovulation and embryo transfer (MOET), such as cow preparation, synchronisation and where only donor cows follow the superovulation protocol. Cows were artificially inseminated and the embryos were flushed and graded. Out of four selected cows for donor, one of them was pregnant and only two cows actuallyproduced the embryos. The recovery rate for the embryo collection was 70.1%, and from 13 embryos (including unfertilised ova), 84.6% of the embryos was classified as good quality and suitable for embryo transfer. The overall results showed that out of eight recipients, five cows were detected pregnant, a 62.5% pregnancy rate. The aim of this report is to describe the procedures aswell as the factors that affect the successful of the MOET programme.

A superovulatory and surgical protocol was developed for recovery of bovine zygotes. Holstein cows and heifers were given follicle-stimulating hormone and cloprostenol to induce superovulation. Surgical cannulation and lavage of the uterine tube was performed 40 to 48 hours after the start of standing estrus. In general, cows had more corpora hemorrhagica than did heifers, but a higher percentage (P < 0.05) of ova recovered from cows were infertile. Several heifers were subjected to the procedure twice, and embryo recovery rates were equivalent both times.

An experiment was conducted to determine whether balancing dietary crude protein for optimal rumen degradability would improve fertilization rate and quality of ova in lactating dairy cows. Thirty-eight Holstein cows in early lactation were fed 1 of 2 diets formulated to be isocaloric and isonitrogenous, containing 16% crude protein. Diet 1 contained 73% rumen degradable intake protein, whereas diet 2 contained 64% rumen degradable intake protein. The cows were induced to superovulate and were inseminated, and ova were recovered nonsurgically on postbreeding day 7. Ova were counted and classified as fertilized or unfertilized. Fertilized ova were scored as excellent, good, fair, poor, or degenerate. Unfertilized ova and poor and degenerate embryos were considered to be nontransferable ova and excellent, good, and fair embryos were considered to be transferable ova. There were no differences for mean number of fertilized, unfertilized, transferable, or nontransferable ova recovered from cows fed the 2 diets (P > 0.10). Mean percentage of fertilized ova recovered from cows was greater (P < 0.05) in those fed diet 2, compared with diet 1. Mean percentage of transferable ova recovered from cows tended to be greater (P = 0.06) in those fed diet 2, compared with diet 1. More cows failed to yield transferable ova (P < 0.05) when fed diet 1, compared with diet 2. Fertilization failure or early degeneration of embryos may occur in cows fed excess rumen degradable protein.

The aim of this study was to evaluate two different superovulation protocols for quality embryo production. Donor animals were selected (Day 0) and a progesterone device was inserted. The superstimulatory treatment was initiated in day 7 (D7) with follicle stimulating hormone from porcine (FSHp) in eight decreasing doses each at 12 hours interval. Along with the fifth dose of FSHp, 500μg cloprostenol was administered. The progesterone device was removed 12h (Treatments P12) and 24 h after the first application of cloprostenol (Treatments P24). Twelve hours after the eighth dose of FSHp (D11) 25µg of Buserelin was administered and the inseminations were done after 12 and 24 hours. Embryos were collected in the forenoon of D18. P24 presented better results than the P12 treatment.

The development and availability of follicles is an indicator to predict which of the follicle sizes are suitable to recover the oocytes assisted by means of ultrasonography of transvaginal oocyte retrieval (OPU). Thus, the study was done in order to characterize the follicular recruitment and distribution in response to the repeated removal of follicles, and thus to determine the availability of follicles and immature oocytes harvested repeatedlyfor two consecutive days of OPU in beef cows. Results indicated that 24-h OPU showed significantly greater numbers of medium and large follicles than small categories (P<0.05). However the 48-hr of OPU does not showed any differences of follicles categories (P>0.05). The mean total number of follicles and immature oocytes recovered were higher (P<0.05) in 24-hr OPU (13.76±1.2 and 7.38 ± 1.7) compared to 48-hr OPU (9.08 ± 1.5 and 3.54 ± 1.00) with the oocyte retrieval rate of 51.22% and 38.17%, respectively. The morphological classification indicated the 24-hr oocyte retrieval produced 62% of suitable immature oocytes that can be used for in vitro embryo production. In conclusion, the repeated removal of two consecutive days of OPU has averted the development of dominant follicle, and thus, gave an atmosphere to the subordinate follicles to continue growth relatively to an equal proportion of small, medium and large categories of follicles. Due to the reduction of follicle and recovery rate at 48-hr it is suggested that OPU be carried out later than 48 hour so that the follicle has more time to increase the diameter size.