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Biology of Reproduction, Vol 4, 145-153, Copyright © 1971 by Society for the Study of Reproduction
1 Reproductive Endocrinology Program, Department of Pathology, The University of Michigan,
Ann Arbor, Michigan
and
Department of Biochemistry, Division of Basic Health Sciences,
Emory University, Atlanta, Georgia A specific and sensitive double-antibody radioimmunoassay for ovine prolactin has been
developed utilizing rabbit antisera to ovine prolactin (NIH-P-S8) and purified ovine prolactin for radioiodination. The assay will quantitate prolactin in pituitary extracts or serum
and will detect as little as 100 pg of prolactin. The activity in serum and pituitary extracts
which inhibited the radioimmunoassay was demonstrated to behave in a similar manner to
purified prolactin-131I by both Sephadex gel filtration and polyacrylamide gel electrophoresis.
Ovine LH, TSH, FSH, and GH do not influence the estimation of prolactin in the radioimmunoassay. Prolactin activity disappeared from the serum after hypophysectomy of ewes.
Exogenous prolactin could be completely recovered when varying amounts were added to a
constant volume of serum. Serum levels of prolactin appear to increase every 3-4 days in
the cycle, and during the first 19 days of pregnancy. There were no differences in circulating
levels of prolactin noted between cyclic and pregnant ewes except for the increased levels
in cyclic ewes at the subsequent estrus. A peak prolactin level was noted on the day of estrus
very near the time of the ovulatory release of luteinizing hormone. In pregnant ewes prolactin levels in serum decreased during the first 2 months, remained very low during the
third and fourth month of gestation (2.0-6.0 ng NIH-P-S8/ml) then began to increase
gradually 3-5 weeks prior to parturition. A dramatic rise in prolactin was noted 3 days
before parturition.
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