The Journal of Clinical Endocrinology & Metabolism · 1974 · 30 citations · 0 references
MedicineEndocrinologyHormone BiochemistryNeuroendocrinologyReproductive EndocrinologyEndocrine DisordersHormone SecretionPituitary DisordersPituitary Gland FunctionPituitary HormonesPituitary TumorsIdiopathic Hypogonadotropic HypogonadismLuteinizing Hormone SecretionPituitary DysfunctionPituitary Endocrine DisordersPituitary Gonadotropin FunctionPituitary Gonadotropin SecretionPituitary Tumor Hormone SecretionSubjects
Synthetic luteinizing hormone-releasing factor was administered intravenously in a dose of 150 μg to 15 normal subjects, 24 subjects with pituitary tumors, 5 subjects with Sheehan's syndrome and 4 subjects with idiopathic hypogonadotropic hypogonadism to evaluate pituitary secretory reserve for LH. In normals plasma LH rose in all individuals from a mean level of 6.4 mIU/ml (range 3.7–10) to a mean level of 55 mIU/ml (range 16–230). In 5 subjects with pituitary tumors who maintained normal gonadotropin secretion, plasma LH levels following LRF rose normally in 4 indicating normal secretory reserve in most subjects. In all subjects with Sheehan's syndrome and idiopathic hypogonadotropic hypogonadism and in 17 of 19 subjects with a pituitary tumor who had reduced gonadotropin secretion plasma LH levels following LRF did not rise or rose subnormally. These data suggest that decreased responsiveness to LRF was the cause of hypogonadotropism in these subjects. In 2 subjects with hypogonadotropism secondary to a pituitary tumor, plasma LH rose normally following LRF. The explanation of decreased gonadotropin secretion in these subjects is not clear but could be the result of defective endogenous LRF production.