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The dual hypothesis of homeostatic body weight regulation, including gravity-dependent and leptin-dependent actions
Body weight is tightly regulated when outside the normal range. It has been proposed that there are individual-specific lower and upper intervention points for when the homeostatic regulation of body weight is initiated. The nature of the homeostatic mechanisms regulating body weight at the lower an...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10475867/ https://www.ncbi.nlm.nih.gov/pubmed/37661748 http://dx.doi.org/10.1098/rstb.2022.0219 |
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author | Jansson, John-Olov Anesten, Frederik Hägg, Daniel Zlatkovic, Jovana Dickson, Suzanne L. Jansson, Per-Anders Schéle, Erik Bellman, Jakob Ohlsson, Claes |
author_facet | Jansson, John-Olov Anesten, Frederik Hägg, Daniel Zlatkovic, Jovana Dickson, Suzanne L. Jansson, Per-Anders Schéle, Erik Bellman, Jakob Ohlsson, Claes |
author_sort | Jansson, John-Olov |
collection | PubMed |
description | Body weight is tightly regulated when outside the normal range. It has been proposed that there are individual-specific lower and upper intervention points for when the homeostatic regulation of body weight is initiated. The nature of the homeostatic mechanisms regulating body weight at the lower and upper ends of the body weight spectrum might differ. Previous studies demonstrate that leptin is the main regulator of body weight at the lower end of the body weight spectrum. We have proposed that land-living animals use gravity to regulate their body weight. We named this homeostatic system the gravitostat and proposed that there are two components of the gravitostat. First, an obvious mechanism involves increased energy consumption in relation to body weight when working against gravity on land. In addition, we propose that there exists a component, involving sensing of the body weight by osteocytes in the weight-bearing bones, resulting in a feedback regulation of energy metabolism and body weight. The gravity-dependent homeostatic regulation is mainly active in obese mice. We, herein, propose the dual hypothesis of body weight regulation, including gravity-dependent actions (= gravitostat) at the upper end and leptin-dependent actions at the lower end of the body weight spectrum. This article is part of a discussion meeting issue ‘Causes of obesity: theories, conjectures and evidence (Part II)’. |
format | Online Article Text |
id | pubmed-10475867 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | The Royal Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-104758672023-09-05 The dual hypothesis of homeostatic body weight regulation, including gravity-dependent and leptin-dependent actions Jansson, John-Olov Anesten, Frederik Hägg, Daniel Zlatkovic, Jovana Dickson, Suzanne L. Jansson, Per-Anders Schéle, Erik Bellman, Jakob Ohlsson, Claes Philos Trans R Soc Lond B Biol Sci Articles Body weight is tightly regulated when outside the normal range. It has been proposed that there are individual-specific lower and upper intervention points for when the homeostatic regulation of body weight is initiated. The nature of the homeostatic mechanisms regulating body weight at the lower and upper ends of the body weight spectrum might differ. Previous studies demonstrate that leptin is the main regulator of body weight at the lower end of the body weight spectrum. We have proposed that land-living animals use gravity to regulate their body weight. We named this homeostatic system the gravitostat and proposed that there are two components of the gravitostat. First, an obvious mechanism involves increased energy consumption in relation to body weight when working against gravity on land. In addition, we propose that there exists a component, involving sensing of the body weight by osteocytes in the weight-bearing bones, resulting in a feedback regulation of energy metabolism and body weight. The gravity-dependent homeostatic regulation is mainly active in obese mice. We, herein, propose the dual hypothesis of body weight regulation, including gravity-dependent actions (= gravitostat) at the upper end and leptin-dependent actions at the lower end of the body weight spectrum. This article is part of a discussion meeting issue ‘Causes of obesity: theories, conjectures and evidence (Part II)’. The Royal Society 2023-10-23 2023-09-04 /pmc/articles/PMC10475867/ /pubmed/37661748 http://dx.doi.org/10.1098/rstb.2022.0219 Text en © 2023 The Authors. https://creativecommons.org/licenses/by/4.0/Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, provided the original author and source are credited. |
spellingShingle | Articles Jansson, John-Olov Anesten, Frederik Hägg, Daniel Zlatkovic, Jovana Dickson, Suzanne L. Jansson, Per-Anders Schéle, Erik Bellman, Jakob Ohlsson, Claes The dual hypothesis of homeostatic body weight regulation, including gravity-dependent and leptin-dependent actions |
title | The dual hypothesis of homeostatic body weight regulation, including gravity-dependent and leptin-dependent actions |
title_full | The dual hypothesis of homeostatic body weight regulation, including gravity-dependent and leptin-dependent actions |
title_fullStr | The dual hypothesis of homeostatic body weight regulation, including gravity-dependent and leptin-dependent actions |
title_full_unstemmed | The dual hypothesis of homeostatic body weight regulation, including gravity-dependent and leptin-dependent actions |
title_short | The dual hypothesis of homeostatic body weight regulation, including gravity-dependent and leptin-dependent actions |
title_sort | dual hypothesis of homeostatic body weight regulation, including gravity-dependent and leptin-dependent actions |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10475867/ https://www.ncbi.nlm.nih.gov/pubmed/37661748 http://dx.doi.org/10.1098/rstb.2022.0219 |
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