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1 Department of Dairy Science, University of Wisconsin, 1675 Observatory Drive, Madison 53706
It was hypothesized that a high dose of estrogen in conjunction with a long-acting PGF2
analog would synchronize parturition within a narrow time frame and reduce the incidence of retained placenta. On d 276 of gestation, 14 animals (9 cows and 5 heifers) per group received a placebo (group A), 1 mg of fenprostalene (group B), 50 mg of estradiol-17ß benzoate (group C), or both (group D). Treatment with estradiol-17ß benzoate increased serum concentrations of estradiol-17ß from 228 pg/ml at treatment to 642 and 683 pg/ml at 24 h posttreatment for groups C and D, respectively. Concentration of estradiol-17ß in group A increased gradually to 526 pg/ml at 24 h prepartum. Progesterone concentrations were reduced by fenprostalene but not by estradiol-17ß benzoate. Estradiol-17ß benzoate did not reduce incidence of retained placenta in animals treated with fenprostalene (group B vs. group D) but tended to reduce incidence in uninduced animals (group A vs. group C). Thus, short-term elevation of estradiol-17ß to normal prepartum concentrations did not regress the corpus luteum, induce parturition, or reduce incidence of retained placenta. However, elevation of estradiol-17ß for longer periods might enhance placental separation. Conversely, fenprostalene induced calving approximately 2 d after treatment. In this study, 90% of animals treated with fenprostalene calved within a 20-h period, but with a high incidence of retained placenta.
Key Words: parturition prostaglandin F2
estradiol retained placenta
Submitted on February 23, 1995
Accepted on August 25, 1995
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