REDUCED GONADOTROPIN SECRETION IN POSTMENOPAUSAL WOMEN DURING TREATMENT WITH A STIMULATORY LRH ANALOGUE
Christer Bergquist, Sven Johan Nillius, LEIF E. WIDE
Abstract
Christer Bergquist, Sven Johan Nillius, LEIF E. WIDE
Abstract
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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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.
Key concepts: Internal medicine, Endocrinology, Agonist, Gonadotropin, Basal (medicine), Estrogen, Gonadotropin-releasing hormone agonist, Gonadotropin-releasing hormone