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Liver but not adipose tissue is responsive to the pattern of enteral feeding
Nutritional support is an important aspect of medical care, providing calories to patients with compromised nutrient intake. Metabolism has a diurnal pattern, responding to the light cycle and food intake, which in turn can drive changes in liver and adipose tissue metabolism. In this study, we asse...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wiley Periodicals, Inc.
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3966249/ https://www.ncbi.nlm.nih.gov/pubmed/24744913 http://dx.doi.org/10.1002/phy2.250 |
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author | Otero, Yolanda F. Lundblad, Tammy M. Ford, Eric A. House, Lawrence M. McGuinness, Owen P. |
author_facet | Otero, Yolanda F. Lundblad, Tammy M. Ford, Eric A. House, Lawrence M. McGuinness, Owen P. |
author_sort | Otero, Yolanda F. |
collection | PubMed |
description | Nutritional support is an important aspect of medical care, providing calories to patients with compromised nutrient intake. Metabolism has a diurnal pattern, responding to the light cycle and food intake, which in turn can drive changes in liver and adipose tissue metabolism. In this study, we assessed the response of liver and white adipose tissue (WAT) to different feeding patterns under nutritional support (total enteral nutrition or TEN). Mice received continuous isocaloric TEN for 10 days or equal calories of chow once a day (Ch). TEN was given either at a constant (CN, same infusion rate during 24 h) or variable rate (VN, 80% of calories fed at night, 20% at day). Hepatic lipogenesis and carbohydrate‐responsive element‐binding protein (ChREBP) expression increased in parallel with the diurnal feeding pattern. Relative to Ch, both patterns of enteral feeding increased adiposity. This increase was not associated with enhanced lipogenic gene expression in WAT; moreover, lipogenesis was unaffected by the feeding pattern. Surprisingly, leptin and adiponectin expression increased. Moreover, nutritional support markedly increased hepatic and adipose FGF21 expression in CN and VN, despite being considered a fasting hormone. In summary, liver but not WAT, respond to the pattern of feeding. While hepatic lipid metabolism adapts to the pattern of nutrient availability, WAT does not. Moreover, sustained delivery of nutrients in an isocaloric diet can cause adiposity without the proinflammatory state observed in hypercaloric feeding. Thus, the liver but not adipose tissue is responsive to the pattern of feeding behavior. |
format | Online Article Text |
id | pubmed-3966249 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Wiley Periodicals, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-39662492014-03-31 Liver but not adipose tissue is responsive to the pattern of enteral feeding Otero, Yolanda F. Lundblad, Tammy M. Ford, Eric A. House, Lawrence M. McGuinness, Owen P. Physiol Rep Original Research Nutritional support is an important aspect of medical care, providing calories to patients with compromised nutrient intake. Metabolism has a diurnal pattern, responding to the light cycle and food intake, which in turn can drive changes in liver and adipose tissue metabolism. In this study, we assessed the response of liver and white adipose tissue (WAT) to different feeding patterns under nutritional support (total enteral nutrition or TEN). Mice received continuous isocaloric TEN for 10 days or equal calories of chow once a day (Ch). TEN was given either at a constant (CN, same infusion rate during 24 h) or variable rate (VN, 80% of calories fed at night, 20% at day). Hepatic lipogenesis and carbohydrate‐responsive element‐binding protein (ChREBP) expression increased in parallel with the diurnal feeding pattern. Relative to Ch, both patterns of enteral feeding increased adiposity. This increase was not associated with enhanced lipogenic gene expression in WAT; moreover, lipogenesis was unaffected by the feeding pattern. Surprisingly, leptin and adiponectin expression increased. Moreover, nutritional support markedly increased hepatic and adipose FGF21 expression in CN and VN, despite being considered a fasting hormone. In summary, liver but not WAT, respond to the pattern of feeding. While hepatic lipid metabolism adapts to the pattern of nutrient availability, WAT does not. Moreover, sustained delivery of nutrients in an isocaloric diet can cause adiposity without the proinflammatory state observed in hypercaloric feeding. Thus, the liver but not adipose tissue is responsive to the pattern of feeding behavior. Wiley Periodicals, Inc. 2014-02-25 /pmc/articles/PMC3966249/ /pubmed/24744913 http://dx.doi.org/10.1002/phy2.250 Text en © 2014 The Authors. Physiological Reports published by Wiley Periodicals, Inc. on behalf of the American Physiological Society and The Physiological Society. http://creativecommons.org/licenses/by/3.0/ This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Research Otero, Yolanda F. Lundblad, Tammy M. Ford, Eric A. House, Lawrence M. McGuinness, Owen P. Liver but not adipose tissue is responsive to the pattern of enteral feeding |
title | Liver but not adipose tissue is responsive to the pattern of enteral feeding |
title_full | Liver but not adipose tissue is responsive to the pattern of enteral feeding |
title_fullStr | Liver but not adipose tissue is responsive to the pattern of enteral feeding |
title_full_unstemmed | Liver but not adipose tissue is responsive to the pattern of enteral feeding |
title_short | Liver but not adipose tissue is responsive to the pattern of enteral feeding |
title_sort | liver but not adipose tissue is responsive to the pattern of enteral feeding |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3966249/ https://www.ncbi.nlm.nih.gov/pubmed/24744913 http://dx.doi.org/10.1002/phy2.250 |
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