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Growth hormone treatment does not augment the anti‐diabetic effects of liraglutide in UCD‐T2DM rats
INTRODUCTION: The incretin hormone glucagon‐like peptide‐1 (GLP‐1) slows gastric emptying, increases satiety and enhances insulin secretion. GLP‐1 receptor agonists, such as liraglutide, are used therapeutically in humans to improve glycaemic control and delay the onset of type 2 diabetes mellitus (...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9836246/ https://www.ncbi.nlm.nih.gov/pubmed/36480511 http://dx.doi.org/10.1002/edm2.392 |
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author | Swarbrick, Michael M. Cox, Chad L. Graham, James L. Knudsen, Lotte B. Stanhope, Kimber Raun, Kirsten Havel, Peter J. |
author_facet | Swarbrick, Michael M. Cox, Chad L. Graham, James L. Knudsen, Lotte B. Stanhope, Kimber Raun, Kirsten Havel, Peter J. |
author_sort | Swarbrick, Michael M. |
collection | PubMed |
description | INTRODUCTION: The incretin hormone glucagon‐like peptide‐1 (GLP‐1) slows gastric emptying, increases satiety and enhances insulin secretion. GLP‐1 receptor agonists, such as liraglutide, are used therapeutically in humans to improve glycaemic control and delay the onset of type 2 diabetes mellitus (T2DM). In UCD‐T2DM rats, a model of polygenic obesity and insulin resistance, we have previously reported that daily liraglutide administration delayed diabetes onset by >4 months. Growth hormone (GH) may exert anti‐diabetic effects, including increasing β‐cell mass and insulin secretion, while disrupting GH signalling in mice reduces both the size and number of pancreatic islets. We therefore hypothesized that GH supplementation would augment liraglutide's anti‐diabetic effects. METHODS: Male UCD‐T2DM rats were treated daily with GH (0.3 mg/kg) and/or liraglutide (0.2 mg/kg) from 2 months of age. Control (vehicle) and food‐restricted (with food intake matched to liraglutide‐treated rats) groups were also studied. The effects of treatment on diabetes onset and weight gain were assessed, as well as measures of glucose tolerance, lipids and islet morphology. RESULTS: Liraglutide treatment significantly reduced food intake and body weight and improved glucose tolerance and insulin sensitivity, relative to controls. After 4.5 months, none of the liraglutide‐treated rats had developed T2DM (overall p = .019). Liraglutide‐treated rats also displayed lower fasting triglyceride (TG) concentrations and lower hepatic TG content, compared to control rats. Islet morphology was improved in liraglutide‐treated rats, with significantly increased pancreatic insulin content (p < .05 vs. controls). Although GH treatment tended to increase body weight (and gastrocnemius muscle weight), there were no obvious effects on diabetes onset or other diabetes‐related outcomes. CONCLUSION: GH supplementation did not augment the anti‐diabetic effects of liraglutide. |
format | Online Article Text |
id | pubmed-9836246 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-98362462023-01-18 Growth hormone treatment does not augment the anti‐diabetic effects of liraglutide in UCD‐T2DM rats Swarbrick, Michael M. Cox, Chad L. Graham, James L. Knudsen, Lotte B. Stanhope, Kimber Raun, Kirsten Havel, Peter J. Endocrinol Diabetes Metab Research Articles INTRODUCTION: The incretin hormone glucagon‐like peptide‐1 (GLP‐1) slows gastric emptying, increases satiety and enhances insulin secretion. GLP‐1 receptor agonists, such as liraglutide, are used therapeutically in humans to improve glycaemic control and delay the onset of type 2 diabetes mellitus (T2DM). In UCD‐T2DM rats, a model of polygenic obesity and insulin resistance, we have previously reported that daily liraglutide administration delayed diabetes onset by >4 months. Growth hormone (GH) may exert anti‐diabetic effects, including increasing β‐cell mass and insulin secretion, while disrupting GH signalling in mice reduces both the size and number of pancreatic islets. We therefore hypothesized that GH supplementation would augment liraglutide's anti‐diabetic effects. METHODS: Male UCD‐T2DM rats were treated daily with GH (0.3 mg/kg) and/or liraglutide (0.2 mg/kg) from 2 months of age. Control (vehicle) and food‐restricted (with food intake matched to liraglutide‐treated rats) groups were also studied. The effects of treatment on diabetes onset and weight gain were assessed, as well as measures of glucose tolerance, lipids and islet morphology. RESULTS: Liraglutide treatment significantly reduced food intake and body weight and improved glucose tolerance and insulin sensitivity, relative to controls. After 4.5 months, none of the liraglutide‐treated rats had developed T2DM (overall p = .019). Liraglutide‐treated rats also displayed lower fasting triglyceride (TG) concentrations and lower hepatic TG content, compared to control rats. Islet morphology was improved in liraglutide‐treated rats, with significantly increased pancreatic insulin content (p < .05 vs. controls). Although GH treatment tended to increase body weight (and gastrocnemius muscle weight), there were no obvious effects on diabetes onset or other diabetes‐related outcomes. CONCLUSION: GH supplementation did not augment the anti‐diabetic effects of liraglutide. John Wiley and Sons Inc. 2022-12-08 /pmc/articles/PMC9836246/ /pubmed/36480511 http://dx.doi.org/10.1002/edm2.392 Text en © 2022 The Authors. Endocrinology, Diabetes & Metabolism published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Swarbrick, Michael M. Cox, Chad L. Graham, James L. Knudsen, Lotte B. Stanhope, Kimber Raun, Kirsten Havel, Peter J. Growth hormone treatment does not augment the anti‐diabetic effects of liraglutide in UCD‐T2DM rats |
title | Growth hormone treatment does not augment the anti‐diabetic effects of liraglutide in UCD‐T2DM rats |
title_full | Growth hormone treatment does not augment the anti‐diabetic effects of liraglutide in UCD‐T2DM rats |
title_fullStr | Growth hormone treatment does not augment the anti‐diabetic effects of liraglutide in UCD‐T2DM rats |
title_full_unstemmed | Growth hormone treatment does not augment the anti‐diabetic effects of liraglutide in UCD‐T2DM rats |
title_short | Growth hormone treatment does not augment the anti‐diabetic effects of liraglutide in UCD‐T2DM rats |
title_sort | growth hormone treatment does not augment the anti‐diabetic effects of liraglutide in ucd‐t2dm rats |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9836246/ https://www.ncbi.nlm.nih.gov/pubmed/36480511 http://dx.doi.org/10.1002/edm2.392 |
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