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1 Roman L. Hruska U.S. Meat Animal
Research Center, Science and Education
Administration-Agricultural Research,
U.S. Department of Agriculture,
Clay Center, Nebraska
A method for the radioimmunoassay of
serum testosterone that does not require extraction or chromatography is described. Utilization of a highly specific antiserum, tritiumlabeled ligand, and double antibody precipitation makes the direct radioimmunoassay
feasible. The direct radioimmunoassay is valid
based on the criteria of sensitivity, specificity,
accuracy, and precision. Because extraction,
chromatography, and transfer are eliminated in
this procedure, recovery of serum testosterone
is always 100%. Interference by serum binding
components is lacking, and values obtained for
ram, bull, dog, rat, and man by direct radioimmunoassay are in agreement with those obtained by a conventional extraction assay.
Direct testosterone radioimmunoassay has
been applied to the study of hypothalamic control of testosterone secretion in bull, ram, and
rat. The intravenous injection of synthetic
luteinizing hormone releasing hormone (LHRH)
increases blood testosterone and can be administered to mimic the pulsatile nature of testosterone secretion characteristic of intact
males. On the other hand, immunoneutralization of LHRH by active or passive immunization
results in substantially reduced serum testosterone and failure of testosterone secretion in
response to exogenous LHRH. These investigations lead us to conclude that testosterone
secretion by the mammalian testis is regulated
largely by inputs from the hypothalamus and
that synthetic LHRH and LHRH antisera provide
useful tools for studying the hypothalamopituitary-gonadal axis. The direct radioimmunoassay provides a convenient and inexpensive method to study testosterone secretion by the testis.
Key words: direct radioimmunoassay, serum testosterone, luteinizing hormone releasing hormone, immunoneutralization
Submitted on May 15, 1981
Revised on June 17, 1981
Accepted on June 23, 1981
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