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The effect of the GLP‐1 analogue Exenatide on functional connectivity within an NTS‐based network in women with and without obesity
OBJECTIVE: The differential effect of GLP‐1 agonist Exenatide on functional connectivity of the nucleus tractus solitaries (NTS), a key region associated with homeostasis, and on appetite‐related behaviours was investigated in women with normal weight compared with women with obesity. METHODS: Follo...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5729499/ https://www.ncbi.nlm.nih.gov/pubmed/29259802 http://dx.doi.org/10.1002/osp4.124 |
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author | Coveleskie, K. Kilpatrick, L. A. Gupta, A. Stains, J. Connolly, L. Labus, J. S. Sanmiguel, C. Mayer, E. A. |
author_facet | Coveleskie, K. Kilpatrick, L. A. Gupta, A. Stains, J. Connolly, L. Labus, J. S. Sanmiguel, C. Mayer, E. A. |
author_sort | Coveleskie, K. |
collection | PubMed |
description | OBJECTIVE: The differential effect of GLP‐1 agonist Exenatide on functional connectivity of the nucleus tractus solitaries (NTS), a key region associated with homeostasis, and on appetite‐related behaviours was investigated in women with normal weight compared with women with obesity. METHODS: Following an 8‐h fast, 19 female subjects (11 lean, 8 obese) participated in a 2‐d double blind crossover study. Subjects underwent functional magnetic resonance imaging at fast and 30‐min post subcutaneous injection of 5 μg of Exenatide or placebo. Functional connectivity was examined with the NTS. Drug‐induced functional connectivity changes within and between groups and correlations with appetite measures were examined in a region of interest approach focusing on the thalamus and hypothalamus. RESULTS: Women with obesity reported less hunger after drug injection. Exenatide administration increased functional connectivity of the left NTS with the left thalamus and hypothalamus in the obese group only and increased the correlation between NTS functional connectivity and hunger scores in all subjects, but more so in the obese. CONCLUSIONS: Obesity can impact the effects of Exenatide on brain connectivity, specifically in the NTS and is linked to changes in appetite control. This has implications for the use of GLP‐1 analogues in therapeutic interventions. |
format | Online Article Text |
id | pubmed-5729499 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-57294992017-12-19 The effect of the GLP‐1 analogue Exenatide on functional connectivity within an NTS‐based network in women with and without obesity Coveleskie, K. Kilpatrick, L. A. Gupta, A. Stains, J. Connolly, L. Labus, J. S. Sanmiguel, C. Mayer, E. A. Obes Sci Pract Original Articles OBJECTIVE: The differential effect of GLP‐1 agonist Exenatide on functional connectivity of the nucleus tractus solitaries (NTS), a key region associated with homeostasis, and on appetite‐related behaviours was investigated in women with normal weight compared with women with obesity. METHODS: Following an 8‐h fast, 19 female subjects (11 lean, 8 obese) participated in a 2‐d double blind crossover study. Subjects underwent functional magnetic resonance imaging at fast and 30‐min post subcutaneous injection of 5 μg of Exenatide or placebo. Functional connectivity was examined with the NTS. Drug‐induced functional connectivity changes within and between groups and correlations with appetite measures were examined in a region of interest approach focusing on the thalamus and hypothalamus. RESULTS: Women with obesity reported less hunger after drug injection. Exenatide administration increased functional connectivity of the left NTS with the left thalamus and hypothalamus in the obese group only and increased the correlation between NTS functional connectivity and hunger scores in all subjects, but more so in the obese. CONCLUSIONS: Obesity can impact the effects of Exenatide on brain connectivity, specifically in the NTS and is linked to changes in appetite control. This has implications for the use of GLP‐1 analogues in therapeutic interventions. John Wiley and Sons Inc. 2017-11-10 /pmc/articles/PMC5729499/ /pubmed/29259802 http://dx.doi.org/10.1002/osp4.124 Text en © 2017 The Authors. Obesity Science & Practice published by John Wiley & Sons Ltd, World Obesity and The Obesity Society. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial (http://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Original Articles Coveleskie, K. Kilpatrick, L. A. Gupta, A. Stains, J. Connolly, L. Labus, J. S. Sanmiguel, C. Mayer, E. A. The effect of the GLP‐1 analogue Exenatide on functional connectivity within an NTS‐based network in women with and without obesity |
title | The effect of the GLP‐1 analogue Exenatide on functional connectivity within an NTS‐based network in women with and without obesity |
title_full | The effect of the GLP‐1 analogue Exenatide on functional connectivity within an NTS‐based network in women with and without obesity |
title_fullStr | The effect of the GLP‐1 analogue Exenatide on functional connectivity within an NTS‐based network in women with and without obesity |
title_full_unstemmed | The effect of the GLP‐1 analogue Exenatide on functional connectivity within an NTS‐based network in women with and without obesity |
title_short | The effect of the GLP‐1 analogue Exenatide on functional connectivity within an NTS‐based network in women with and without obesity |
title_sort | effect of the glp‐1 analogue exenatide on functional connectivity within an nts‐based network in women with and without obesity |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5729499/ https://www.ncbi.nlm.nih.gov/pubmed/29259802 http://dx.doi.org/10.1002/osp4.124 |
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