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Biology of Reproduction, Vol 14, 495-501, Copyright © 1976 by Society for the Study of Reproduction
1 Reproductive Physiology,
Oregon Regional Primate Research Center,
Beaverton, Oregon 97005 Serum concentrations of prolactin, LH, estradiol, and progesterone were measured daily
throughout one or more menstrual cycles in 7 rhesus monkeys. Prolactin concentrations at 0800 - 0900 h during 13 menstrual cycles averaged 10.7 ± 0.2 ng/ml (± SE). During none of the cycles did
a significant rise in serum prolactin occur to coincide with preovulatory surges in estradiol (368 ±
29 pg/ml) and LH (4.2 ± 0.6 ng/ml). However the mean prolactin level during the follicular phase
of all cycles (10.1 ± 0.4 ng/ml) was slightly (P>0.05) lower than that during the luteal phase (11.2
± 0.4 ng/ml) when progesterone levels were elevated. The 24 h pattern of serum prolactin was determined in 6 female monkeys bled at 4 h intervals
during a 24 h period and then again a week later at 12 h intervals at 0800 and 2000 h on Day 1, at
1200 and 2400 h on Day 2, and at 1600 and 0400 h on Day 3. Under both bleeding frequencies
serum prolactin concentrations showed a marked nyctohemeral rhythm with high levels during the
night and low levels during the day. The overall average was 10.4 ± 0.5 ng/ml during the day and
17.3 ± 0.9 ng/ml during the night (P<0.001). Moreover, serum prolactin levels at any of the 3
times during the day (0800, 1200, 1600 h) were significantly lower (P<0.001) compared to those
at the 3 times (2000, 2400, and 0400 h) during the night. The 24 h pattern of serum prolactin concentrations was remarkably similar under both bleeding intervals except for slight depressions at
1200 and 2400 h under the shorter bleeding interval. The stage of the menstrual cycle had no effect on the nyctohemeral rhythm as judged by 24 h profiles of serum prolactin during the luteal
(Days 19-22) and follicular (Days 5-8) phases of the menstrual cycle. These results indicate the
suitability of the rhesus monkey as a model to study the neural mechanisms involved in the diurnal
changes in prolactin release in primates.
Note:
ACKNOWLEDGMENTS
We are indebted to Dr. John A. Resko for the
steroid data and are thankful to Terry T. Oyama and
Margaret K. Stobie for technical assistance.
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