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Biology of Reproduction, Vol 25, 568-572, Copyright © 1981 by Society for the Study of Reproduction
1 Department of Physiology,
University of Arizona, Health Sciences Center,
Tucson, Arizona 85724. Primate gonadotropins [human luteinizing hormone (hLH) and chorionic gonadotropin (hCG)]
were 500-1000 times more effective than nonprimate gonadotropins (ovine, bovine, and porcine
LH) in inhibiting 125 I-hLH binding to particulate preparations of the corpus luteum from the
rhesus monkey. In contrast, all gonadotropins were equipotent in inhibiting 125 I-hLH binding to
luteinized ovarian tissue from pregnant rats. Moreover, primate gonadotropins were only 10 times
more effective than nonprimate gonadotropins in competing for LH binding sites in porcine
corpora lutea. This comparative study indicates that the apparent species specificity of gonadotropin receptors in the monkey is not due to differences in purity or biological activity (as measured in the rat OAAD bioassay) between hormone preparations. Rather, primate gonadotropin
receptors have an increased affinity for primate gonadotropins and a decreased affinity for nonprimate hormones. This study emphasizes that the investigation of gonadotropin action in primate
reproduction requires the use of primate gonadotropins.
Note:
ACKNOWLEDGMENTS
The authors would like to thank Dr. David E. Blask
for his assistance with the rat studies, Barbara Torres
for her excellent technical assistance, and Gayle
Caulton for her preparation of the manuscript. This
work was supported by NIH Grants HD-12333, BRSG
(RO-5675), and HL-O7249 and an Upjohn Graduate
Fellowship in Physiology.
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