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The potent and long-acting LRH agonist D-Ser(TBU)6-EA10-LRH was administered in a daily subcutaneous dose of 5 microgram to 5 postmenopausal women for a period of 10 days. The LRH analogue produced a significant decrease in both the basal FSH and LH levels and the gonadotropin responses to the agonist. The estrogen levels in serum remained unchanged during the study period. The results suggest that D-Ser(TBU)6-EA10-LRH has a direct inhibitory effect at the pituitary level.
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Christer Bergquist
Uppsala University Hospital
Sven Johan Nillius
Uppsala University Hospital
Leif Wide
Uppsala University Hospital
The Journal of Clinical Endocrinology & Metabolism
Uppsala University Hospital
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Bergquist et al. (Sat,) studied this question.
synapsesocial.com/papers/6a1eb8385dae381e029a816e — DOI: https://doi.org/10.1210/jcem-49-3-472