Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Otero, Yolanda F., Lundblad, Tammy M., Ford, Eric A., House, Lawrence M., McGuinness, Owen P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wiley Periodicals, Inc. 2014
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
_version_ 1782308884513292288
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
work_keys_str_mv AT oteroyolandaf liverbutnotadiposetissueisresponsivetothepatternofenteralfeeding
AT lundbladtammym liverbutnotadiposetissueisresponsivetothepatternofenteralfeeding
AT forderica liverbutnotadiposetissueisresponsivetothepatternofenteralfeeding
AT houselawrencem liverbutnotadiposetissueisresponsivetothepatternofenteralfeeding
AT mcguinnessowenp liverbutnotadiposetissueisresponsivetothepatternofenteralfeeding