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Biology of Reproduction, Vol 15, 141-146, Copyright © 1976 by Society for the Study of Reproduction
1 Medical Research Center, Prince Henry’s Hospital,
Melbourne, 3004,
Reproduction Research Section, University of Melbourne,
and Department of Agriculture,
S. S. Cameron Laboratory, Werribee, 3030,
and Howard Florey Institute of Experimental Physiology and Medicine,
University of Melbourne, 3052 Luteinizing hormone releasing hormone (LHRH) was administered to adult rams as constant
intravenous infusions lasting 4 to 6 h. Dosages of 0.05, 0.1, 0.5 and 1.0 ug/min were used. All
studies were undertaken during the period of decreasing day length (January to June). Plasma
luteinizing hormone (LH) values during administration of the two highest dosages revealed a
biphasic pattern of increase during the first 2 h of the infusion, as has been found in similar studies
in humans. LH values were maximal at approximately 2 Plasma testosterone (T) levels increased sharply 15-30 min after the initial rise in LH values.
Maximal levels of T obtained were 3- to 5-fold greater than basal values and were considerably
higher than those found during similar studies in men. These results suggest that T production from
the ram testis is more sensitive to gonadotrophin stimulation than is that from the human testis. In
spite of the prolonged elevations in gonadotrophins and the marked increases in plasma T levels,
plasma estradiol levels were consistently close to or below assay sensitivity (15 pg/ml).
h of the infusions, then decreased in
spite of continued LHRH administration, thereby demonstrating the development of pituitary
refractoriness during prolonged LHRH administration. A similar refractory period has not been
noted during analogous studies in men. Plasma follicle stimulating hormone (FSH) values generally
increased gradually during LHRH infusions, with no evidence of a biphasic pattern. No FSH
increase was noted in some studies, even at the highest LHRH dosage used.
Note:
ACKNOWLEDGMENTS
We appreciate the technical assistance of Mrs. Anne
Davies, Ms. Ausma Dulmanis, Mr. Peter Langdon and
Mr. R. W. Baxter, the typing of Mrs. Jill Volfsbergs
and the illustrations of Ms. Anne Hayres. We are
grateful to Dr. H. Papkoff for his gift of highly
purified ovine FSH (49 x NIH-FSH-S1) and ovine LH
(2 x NIH-LH-S1), to Hoechst Pharmaceuticals for
their gift of synthetic LHRH, and to the National
Institutes of Health for their gift of the gonadotrophin
standards. This work was supported by grants from
the National Health and Medical Research Council of
Australia and the Australian Wool Research Trust
Fund.
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