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Evaluation of Pregnancy Rates of Dairy Heifers Receiving IVP Embryos with or without Supplemental Progesterone
Evaluation of Pregnancy Rates of Dairy Heifers Receiving IVP Embryos with or without Supplemental Progesterone
Wednesday, March 14, 2018
Grand Ballroom Foyer (CenturyLink Convention Center)
Pregnancy rates after the transfer of frozen-thawed, in vitro produced (IVP) embryos are less than ideal. The objective of this study was to determine whether the addition a controlled internal drug release (CIDR) device at the time of transfer of IVP embryos influenced pregnancy rates of dairy heifers. A total of 439 Holstein heifers (479 ± 33 d of age) were included in this study. Estrous cycles of heifers were synchronized and those detected in estrus with a viable corpus luteum each received a frozen-thawed IVP embryo 7.1 ± 0.47 d after detected estrus (d 0). At the time of transfer, heifers were stratified by the donor flush group of the embryo they received, and then randomly assigned to 1 of 2 treatment groups: 1) received no supplementation (control; n = 211), or 2) received supplemental progesterone via a CIDR device from d 7 (immediately after transfer) until d 19 post-estrus (CIDR; n = 228). Transrectal ultrasonography and rectal palpation were performed at approximately d 30 and d 60 post-estrus, respectively, to determine pregnancy status. Developmental stage, grade, and parentage of all embryos were recorded. Data were analyzed using the GLIMMIX procedure of SAS; means are presented. Overall pregnancy rates were 27.5% on d 30 but were reduced by d 60 to 23.3%. Supplementation of progesterone did not affect pregnancy rates on either d 30 (P = 0.467; 26.5 vs 28.1%, for control and CIDR, respectively), or d 60 (P = 0.417; 24.9 vs 21.5%, for control and CIDR, respectively). Embryo parentage, grade or developmental stage or BCS of recipient heifers did not influence (P ≥ 0.105) pregnancy rates. In conclusion, supplemental progesterone via a CIDR device did not alter pregnancy rates after the transfer of IVP embryos. Further research is necessary to elucidate mechanisms to increase the viability of IVP embryos.