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Acute Recapitulation of the Hyperinsulinemia and Hyperlipidemia characteristic of Metabolic Syndrome suppresses Gonadotropins
OBJECTIVE: To determine the effect of lipid/heparin versus saline infusion, with or without concurrent euglycemic hyperinsulinemia on serum FSH and LH. Obesity is associated with hyperlipidemia, insulin resistance, and relative hypogonadotropic hypogonadism. We hypothesized that acutely elevated fat...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5323271/ https://www.ncbi.nlm.nih.gov/pubmed/28158916 http://dx.doi.org/10.1002/oby.21754 |
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author | Chosich, Justin Bradford, Andrew P. Allshouse, Amanda A Reusch, Jane E. B. Santoro, Nanette Schauer, Irene E |
author_facet | Chosich, Justin Bradford, Andrew P. Allshouse, Amanda A Reusch, Jane E. B. Santoro, Nanette Schauer, Irene E |
author_sort | Chosich, Justin |
collection | PubMed |
description | OBJECTIVE: To determine the effect of lipid/heparin versus saline infusion, with or without concurrent euglycemic hyperinsulinemia on serum FSH and LH. Obesity is associated with hyperlipidemia, insulin resistance, and relative hypogonadotropic hypogonadism. We hypothesized that acutely elevated fatty acids and insulin would impair gonadotropin secretion. METHODS: Regularly cycling women and men who were non-obese underwent a crossover 6-hour infusion study over 4 visits. Participants received infusions of: saline-control, lipid/heparin, insulin and lipid/heparin plus insulin. Serum FSH and LH were measured by immunoassay. RESULTS: In women (n=10), infusion of lipid plus insulin significantly reduced LH, from 4.6 (3.7-5.4) [mean (95% confidence interval)] to 3.3 (2.3-4.4); p=0.03 and FSH from 3.9 (3.2-4.6) to 3.1, (2.3-3.8) IU/L; p=0.03 compared to saline-control. Similarly, in men (n=10), LH, 3.3 (2.4-4.1) IU/L and FSH, 2.1 (1.4-2.8) IU/L were significantly reduced after the combined infusion, (2.2 (1.3-3.1) IU/L and 1.5 (0.8-2.1) IU/L; p=0.03, p=0.02, respectively). Neither lipid nor insulin alone significantly impacted gonadotropin levels compared to saline-control. CONCLUSIONS: Hyperinsulinemia combined with elevated lipids acutely suppresses LH and FSH, providing a possible mechanism underlying the relative hypogonadotropic hypogonadism of obesity. Effects of insulin on the hypothalamic-pituitary-gonadal axis may be dependent on the concomitant metabolic environment. |
format | Online Article Text |
id | pubmed-5323271 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
record_format | MEDLINE/PubMed |
spelling | pubmed-53232712017-08-03 Acute Recapitulation of the Hyperinsulinemia and Hyperlipidemia characteristic of Metabolic Syndrome suppresses Gonadotropins Chosich, Justin Bradford, Andrew P. Allshouse, Amanda A Reusch, Jane E. B. Santoro, Nanette Schauer, Irene E Obesity (Silver Spring) Article OBJECTIVE: To determine the effect of lipid/heparin versus saline infusion, with or without concurrent euglycemic hyperinsulinemia on serum FSH and LH. Obesity is associated with hyperlipidemia, insulin resistance, and relative hypogonadotropic hypogonadism. We hypothesized that acutely elevated fatty acids and insulin would impair gonadotropin secretion. METHODS: Regularly cycling women and men who were non-obese underwent a crossover 6-hour infusion study over 4 visits. Participants received infusions of: saline-control, lipid/heparin, insulin and lipid/heparin plus insulin. Serum FSH and LH were measured by immunoassay. RESULTS: In women (n=10), infusion of lipid plus insulin significantly reduced LH, from 4.6 (3.7-5.4) [mean (95% confidence interval)] to 3.3 (2.3-4.4); p=0.03 and FSH from 3.9 (3.2-4.6) to 3.1, (2.3-3.8) IU/L; p=0.03 compared to saline-control. Similarly, in men (n=10), LH, 3.3 (2.4-4.1) IU/L and FSH, 2.1 (1.4-2.8) IU/L were significantly reduced after the combined infusion, (2.2 (1.3-3.1) IU/L and 1.5 (0.8-2.1) IU/L; p=0.03, p=0.02, respectively). Neither lipid nor insulin alone significantly impacted gonadotropin levels compared to saline-control. CONCLUSIONS: Hyperinsulinemia combined with elevated lipids acutely suppresses LH and FSH, providing a possible mechanism underlying the relative hypogonadotropic hypogonadism of obesity. Effects of insulin on the hypothalamic-pituitary-gonadal axis may be dependent on the concomitant metabolic environment. 2017-02-03 2017-03 /pmc/articles/PMC5323271/ /pubmed/28158916 http://dx.doi.org/10.1002/oby.21754 Text en http://www.nature.com/authors/editorial_policies/license.html#terms Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Chosich, Justin Bradford, Andrew P. Allshouse, Amanda A Reusch, Jane E. B. Santoro, Nanette Schauer, Irene E Acute Recapitulation of the Hyperinsulinemia and Hyperlipidemia characteristic of Metabolic Syndrome suppresses Gonadotropins |
title | Acute Recapitulation of the Hyperinsulinemia and Hyperlipidemia characteristic of Metabolic Syndrome suppresses Gonadotropins |
title_full | Acute Recapitulation of the Hyperinsulinemia and Hyperlipidemia characteristic of Metabolic Syndrome suppresses Gonadotropins |
title_fullStr | Acute Recapitulation of the Hyperinsulinemia and Hyperlipidemia characteristic of Metabolic Syndrome suppresses Gonadotropins |
title_full_unstemmed | Acute Recapitulation of the Hyperinsulinemia and Hyperlipidemia characteristic of Metabolic Syndrome suppresses Gonadotropins |
title_short | Acute Recapitulation of the Hyperinsulinemia and Hyperlipidemia characteristic of Metabolic Syndrome suppresses Gonadotropins |
title_sort | acute recapitulation of the hyperinsulinemia and hyperlipidemia characteristic of metabolic syndrome suppresses gonadotropins |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5323271/ https://www.ncbi.nlm.nih.gov/pubmed/28158916 http://dx.doi.org/10.1002/oby.21754 |
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