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FRI002 IGF-1R Targeting As A Strategy For Reducing Obesity And Improving Metabolism
Disclosure: S. Al-Samerria: None. S. Farooq: None. N. Nandankar: None. A.L. Negron: None. S. Radovick: None. There has been a significant increase in the prevalence of obesity over the past four decades, and it is projected that by 2030, the majority of the global population will fall into the overw...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10555443/ http://dx.doi.org/10.1210/jendso/bvad114.014 |
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author | Al-Samerria, Sarmed Farooq, Saad Candidate, M S Nandankar, Nimisha Negron, Ariel Negron L Radovick, Sally |
author_facet | Al-Samerria, Sarmed Farooq, Saad Candidate, M S Nandankar, Nimisha Negron, Ariel Negron L Radovick, Sally |
author_sort | Al-Samerria, Sarmed |
collection | PubMed |
description | Disclosure: S. Al-Samerria: None. S. Farooq: None. N. Nandankar: None. A.L. Negron: None. S. Radovick: None. There has been a significant increase in the prevalence of obesity over the past four decades, and it is projected that by 2030, the majority of the global population will fall into the overweight or obese categories if this trend continues. In a previous study, we reported that the ablation of the IGF-1R in GHRH neurons and somatotrophs (S-GIGFRKO) resulted in a sustained decrease in weight gain velocity due to increased lipolysis and higher energy expenditure, despite no changes in caloric intake. To evaluate the effects of a high-fat diet (HFD) on this metabolic phenotype, we challenged S-GIGFRKO mice with a 60% HFD beginning at 4 weeks of age. The S-GIGFRKO mice on the HFD showed normal linear growth, but after 8 weeks on the HFD, both males and females exhibited a sustained decrease in weight gain velocity compared to control mice on the HFD. Metabolic analysis revealed that the male and female S-GIGFRKO mice had higher oxygen consumption, lower carbon dioxide production, reduced body fat mass, increased energy expenditure, and improved glucose tolerance compared to the control mice on the HFD. No differences in food intake or total activity were observed between the two groups. These results demonstrate the important role of the GHRH-GH axis in regulating energy expenditure and fat metabolism, despite an environmental challenge induced by a HFD. Presentation: Friday, June 16, 2023 |
format | Online Article Text |
id | pubmed-10555443 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-105554432023-10-06 FRI002 IGF-1R Targeting As A Strategy For Reducing Obesity And Improving Metabolism Al-Samerria, Sarmed Farooq, Saad Candidate, M S Nandankar, Nimisha Negron, Ariel Negron L Radovick, Sally J Endocr Soc Adipose Tissue, Appetite, & Obesity Disclosure: S. Al-Samerria: None. S. Farooq: None. N. Nandankar: None. A.L. Negron: None. S. Radovick: None. There has been a significant increase in the prevalence of obesity over the past four decades, and it is projected that by 2030, the majority of the global population will fall into the overweight or obese categories if this trend continues. In a previous study, we reported that the ablation of the IGF-1R in GHRH neurons and somatotrophs (S-GIGFRKO) resulted in a sustained decrease in weight gain velocity due to increased lipolysis and higher energy expenditure, despite no changes in caloric intake. To evaluate the effects of a high-fat diet (HFD) on this metabolic phenotype, we challenged S-GIGFRKO mice with a 60% HFD beginning at 4 weeks of age. The S-GIGFRKO mice on the HFD showed normal linear growth, but after 8 weeks on the HFD, both males and females exhibited a sustained decrease in weight gain velocity compared to control mice on the HFD. Metabolic analysis revealed that the male and female S-GIGFRKO mice had higher oxygen consumption, lower carbon dioxide production, reduced body fat mass, increased energy expenditure, and improved glucose tolerance compared to the control mice on the HFD. No differences in food intake or total activity were observed between the two groups. These results demonstrate the important role of the GHRH-GH axis in regulating energy expenditure and fat metabolism, despite an environmental challenge induced by a HFD. Presentation: Friday, June 16, 2023 Oxford University Press 2023-10-05 /pmc/articles/PMC10555443/ http://dx.doi.org/10.1210/jendso/bvad114.014 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of the Endocrine Society. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (https://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Adipose Tissue, Appetite, & Obesity Al-Samerria, Sarmed Farooq, Saad Candidate, M S Nandankar, Nimisha Negron, Ariel Negron L Radovick, Sally FRI002 IGF-1R Targeting As A Strategy For Reducing Obesity And Improving Metabolism |
title | FRI002 IGF-1R Targeting As A Strategy For Reducing Obesity And Improving Metabolism |
title_full | FRI002 IGF-1R Targeting As A Strategy For Reducing Obesity And Improving Metabolism |
title_fullStr | FRI002 IGF-1R Targeting As A Strategy For Reducing Obesity And Improving Metabolism |
title_full_unstemmed | FRI002 IGF-1R Targeting As A Strategy For Reducing Obesity And Improving Metabolism |
title_short | FRI002 IGF-1R Targeting As A Strategy For Reducing Obesity And Improving Metabolism |
title_sort | fri002 igf-1r targeting as a strategy for reducing obesity and improving metabolism |
topic | Adipose Tissue, Appetite, & Obesity |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10555443/ http://dx.doi.org/10.1210/jendso/bvad114.014 |
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