Estradiol potentiates ghrelin-stimulated pulsatile growth hormone secretion in postmenopausal women.

نویسندگان

  • Johannes D Veldhuis
  • Daniel M Keenan
  • Ali Iranmanesh
  • Kristi Mielke
  • John M Miles
  • Cyril Y Bowers
چکیده

CONTEXT Ghrelin and an estrogen-rich milieu individually amplify pulsatile GH secretion by increasing the amount of hormone released per burst. However, how these distinct agonists interact in controlling pulsatile GH output is not known. OBJECTIVE The objective of the study was to test the hypothesis that elevated estradiol (E(2)) concentrations potentiate hypothalamo-pituitary responses to a near-physiological ghrelin stimulus. DESIGN This was a double-blind, placebo-controlled, prospectively randomized, parallel-cohort study. SETTING The study was conducted at an academic medical center. SUBJECTS Twenty-one postmenopausal women participated in the study. INTERVENTIONS Eleven subjects received placebo (Pl) and 10 others E(2) transdermally in escalating doses over 3 wk to mimic late follicular-phase E(2) concentrations. Saline or a submaximally stimulatory amount of ghrelin (0.3 microg/kg) was infused iv on separate randomly ordered mornings fasting after 17-21 d of Pl or E(2) administration. OUTCOMES Outcomes included serum concentrations of E(2), ghrelin, GH, IGF-I, IGF binding protein (IGFBP)-1 and IGFBP-3, and the estimated mass and waveform of stimulated GH secretory bursts. RESULTS Administration of E(2) yielded late follicular-phase E(2) concentrations. Compared with Pl, E(2) did not alter ghrelin concentrations but reduced IGF-I and IGFBP-3 and elevated IGFBP-1 concentrations. Compared with saline, ghrelin infusion amplified pulsatile GH secretion by 7.1-fold (P < 0.01). The effect of E(2) alone was 2.0-fold placebo and that of combined ghrelin/E(2) 10.4-fold (P < 0.01). Ghrelin and E(2) accelerated initial GH release individually but nonadditively by more than 2-fold (P < 0.01). CONCLUSIONS Estrogen augments ghrelin's near-physiological stimulation of pulsatile GH secretion and mimics ghrelin's acceleration of initial GH release. Thus, we hypothesize that estrogen and a GH secretagogue act via independent as well as convergent mechanisms.

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عنوان ژورنال:
  • The Journal of clinical endocrinology and metabolism

دوره 91 9  شماره 

صفحات  -

تاریخ انتشار 2006