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Feedback on LH in Testosterone-Clamped Men Depends on the Mode of Testosterone Administration and Body Composition

CONTEXT: Quantitative studies of the short-term feedback of testosterone (T) on luteinizing hormone (LH) secretion in healthy men are relatively rare. Such studies require the shutting down of endogenous T secretion and the imposition of experimentally controlled IV T addback. OBJECTIVE: To evaluate...

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Detalles Bibliográficos
Autores principales: Roelfsema, Ferdinand, Yang, Rebecca J, Liu, Peter Y, Takahashi, Paul Y, Veldhuis, Johannes D
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Endocrine Society 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6320245/
https://www.ncbi.nlm.nih.gov/pubmed/30623162
http://dx.doi.org/10.1210/js.2018-00317
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author Roelfsema, Ferdinand
Yang, Rebecca J
Liu, Peter Y
Takahashi, Paul Y
Veldhuis, Johannes D
author_facet Roelfsema, Ferdinand
Yang, Rebecca J
Liu, Peter Y
Takahashi, Paul Y
Veldhuis, Johannes D
author_sort Roelfsema, Ferdinand
collection PubMed
description CONTEXT: Quantitative studies of the short-term feedback of testosterone (T) on luteinizing hormone (LH) secretion in healthy men are relatively rare. Such studies require the shutting down of endogenous T secretion and the imposition of experimentally controlled IV T addback. OBJECTIVE: To evaluate whether pulsatile and continuous T delivery confers equivalent negative feedback on LH secretion. DESIGN: This was a placebo-controlled, blinded, and prospectively randomized crossover study comprising 16 healthy men [age range 23 to 54 years and a body mass index (BMI) between 22.3 and 34.2 kg/m(2)]. Subjects received ketoconazole to block endogenous T secretion and received continuous or 90-minute pulses of IV T addback. SETTING: The study was performed in a Clinical Translational Research Unit. INTERVENTIONS: Subjects underwent 14 hours of blood sampling at 10-minute intervals, with a bolus IV injection of 33 ng/kg gonadotropin-releasing hormone (GnRH). MAIN OUTCOME MEASURES: Log-transformed LH and T concentration ratios before and after GnRH administration. RESULTS: Despite higher T concentrations during pulsatile T feedback, LH concentrations and secretion rates, whether driven by endogenous or exogenous GnRH, were similar to those during continuous T infusion, indicating diminished pulsatile T feedback. Feedback correlated negatively with BMI. Under controlled T feedback, basal but not pulsatile LH secretion correlated negatively with CT-estimated visceral fat mass. CONCLUSION: Feedback by pulsatile T delivery has diminished inhibitory strength compared with continuous infusion. Feedback is negatively correlated with BMI.
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spelling pubmed-63202452019-01-08 Feedback on LH in Testosterone-Clamped Men Depends on the Mode of Testosterone Administration and Body Composition Roelfsema, Ferdinand Yang, Rebecca J Liu, Peter Y Takahashi, Paul Y Veldhuis, Johannes D J Endocr Soc Clinical Research Articles CONTEXT: Quantitative studies of the short-term feedback of testosterone (T) on luteinizing hormone (LH) secretion in healthy men are relatively rare. Such studies require the shutting down of endogenous T secretion and the imposition of experimentally controlled IV T addback. OBJECTIVE: To evaluate whether pulsatile and continuous T delivery confers equivalent negative feedback on LH secretion. DESIGN: This was a placebo-controlled, blinded, and prospectively randomized crossover study comprising 16 healthy men [age range 23 to 54 years and a body mass index (BMI) between 22.3 and 34.2 kg/m(2)]. Subjects received ketoconazole to block endogenous T secretion and received continuous or 90-minute pulses of IV T addback. SETTING: The study was performed in a Clinical Translational Research Unit. INTERVENTIONS: Subjects underwent 14 hours of blood sampling at 10-minute intervals, with a bolus IV injection of 33 ng/kg gonadotropin-releasing hormone (GnRH). MAIN OUTCOME MEASURES: Log-transformed LH and T concentration ratios before and after GnRH administration. RESULTS: Despite higher T concentrations during pulsatile T feedback, LH concentrations and secretion rates, whether driven by endogenous or exogenous GnRH, were similar to those during continuous T infusion, indicating diminished pulsatile T feedback. Feedback correlated negatively with BMI. Under controlled T feedback, basal but not pulsatile LH secretion correlated negatively with CT-estimated visceral fat mass. CONCLUSION: Feedback by pulsatile T delivery has diminished inhibitory strength compared with continuous infusion. Feedback is negatively correlated with BMI. Endocrine Society 2018-11-23 /pmc/articles/PMC6320245/ /pubmed/30623162 http://dx.doi.org/10.1210/js.2018-00317 Text en Copyright © 2019 Endocrine Society https://creativecommons.org/licenses/by-nc-nd/4.0/ This article has been published under the terms of the Creative Commons Attribution Non-Commercial, No-Derivatives License (CC BY-NC-ND; https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Clinical Research Articles
Roelfsema, Ferdinand
Yang, Rebecca J
Liu, Peter Y
Takahashi, Paul Y
Veldhuis, Johannes D
Feedback on LH in Testosterone-Clamped Men Depends on the Mode of Testosterone Administration and Body Composition
title Feedback on LH in Testosterone-Clamped Men Depends on the Mode of Testosterone Administration and Body Composition
title_full Feedback on LH in Testosterone-Clamped Men Depends on the Mode of Testosterone Administration and Body Composition
title_fullStr Feedback on LH in Testosterone-Clamped Men Depends on the Mode of Testosterone Administration and Body Composition
title_full_unstemmed Feedback on LH in Testosterone-Clamped Men Depends on the Mode of Testosterone Administration and Body Composition
title_short Feedback on LH in Testosterone-Clamped Men Depends on the Mode of Testosterone Administration and Body Composition
title_sort feedback on lh in testosterone-clamped men depends on the mode of testosterone administration and body composition
topic Clinical Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6320245/
https://www.ncbi.nlm.nih.gov/pubmed/30623162
http://dx.doi.org/10.1210/js.2018-00317
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