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The Role of Liver Fructose-1,6-Bisphosphatase in Regulating Appetite and Adiposity
Liver fructose-1,6-bisphosphatase (FBPase) is a regulatory enzyme in gluconeogenesis that is elevated by obesity and dietary fat intake. Whether FBPase functions only to regulate glucose or has other metabolic consequences is not clear; therefore, the aim of this study was to determine the importanc...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Diabetes Association
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3331739/ https://www.ncbi.nlm.nih.gov/pubmed/22517657 http://dx.doi.org/10.2337/db11-1511 |
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author | Visinoni, Sherley Khalid, Nurul Fathiah Izzati Joannides, Christos N. Shulkes, Arthur Yim, Mildred Whitehead, Jon Tiganis, Tony Lamont, Benjamin J. Favaloro, Jenny M. Proietto, Joseph Andrikopoulos, Sofianos Fam, Barbara C. |
author_facet | Visinoni, Sherley Khalid, Nurul Fathiah Izzati Joannides, Christos N. Shulkes, Arthur Yim, Mildred Whitehead, Jon Tiganis, Tony Lamont, Benjamin J. Favaloro, Jenny M. Proietto, Joseph Andrikopoulos, Sofianos Fam, Barbara C. |
author_sort | Visinoni, Sherley |
collection | PubMed |
description | Liver fructose-1,6-bisphosphatase (FBPase) is a regulatory enzyme in gluconeogenesis that is elevated by obesity and dietary fat intake. Whether FBPase functions only to regulate glucose or has other metabolic consequences is not clear; therefore, the aim of this study was to determine the importance of liver FBPase in body weight regulation. To this end we performed comprehensive physiologic and biochemical assessments of energy balance in liver-specific transgenic FBPase mice and negative control littermates of both sexes. In addition, hepatic branch vagotomies and pharmacologic inhibition studies were performed to confirm the role of FBPase. Compared with negative littermates, liver-specific FBPase transgenic mice had 50% less adiposity and ate 15% less food but did not have altered energy expenditure. The reduced food consumption was associated with increased circulating leptin and cholecystokinin, elevated fatty acid oxidation, and 3-β-hydroxybutyrate ketone levels, and reduced appetite-stimulating neuropeptides, neuropeptide Y and Agouti-related peptide. Hepatic branch vagotomy and direct pharmacologic inhibition of FBPase in transgenic mice both returned food intake and body weight to the negative littermates. This is the first study to identify liver FBPase as a previously unknown regulator of appetite and adiposity and describes a novel process by which the liver participates in body weight regulation. |
format | Online Article Text |
id | pubmed-3331739 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | American Diabetes Association |
record_format | MEDLINE/PubMed |
spelling | pubmed-33317392013-05-01 The Role of Liver Fructose-1,6-Bisphosphatase in Regulating Appetite and Adiposity Visinoni, Sherley Khalid, Nurul Fathiah Izzati Joannides, Christos N. Shulkes, Arthur Yim, Mildred Whitehead, Jon Tiganis, Tony Lamont, Benjamin J. Favaloro, Jenny M. Proietto, Joseph Andrikopoulos, Sofianos Fam, Barbara C. Diabetes Obesity Studies Liver fructose-1,6-bisphosphatase (FBPase) is a regulatory enzyme in gluconeogenesis that is elevated by obesity and dietary fat intake. Whether FBPase functions only to regulate glucose or has other metabolic consequences is not clear; therefore, the aim of this study was to determine the importance of liver FBPase in body weight regulation. To this end we performed comprehensive physiologic and biochemical assessments of energy balance in liver-specific transgenic FBPase mice and negative control littermates of both sexes. In addition, hepatic branch vagotomies and pharmacologic inhibition studies were performed to confirm the role of FBPase. Compared with negative littermates, liver-specific FBPase transgenic mice had 50% less adiposity and ate 15% less food but did not have altered energy expenditure. The reduced food consumption was associated with increased circulating leptin and cholecystokinin, elevated fatty acid oxidation, and 3-β-hydroxybutyrate ketone levels, and reduced appetite-stimulating neuropeptides, neuropeptide Y and Agouti-related peptide. Hepatic branch vagotomy and direct pharmacologic inhibition of FBPase in transgenic mice both returned food intake and body weight to the negative littermates. This is the first study to identify liver FBPase as a previously unknown regulator of appetite and adiposity and describes a novel process by which the liver participates in body weight regulation. American Diabetes Association 2012-05 2012-04-13 /pmc/articles/PMC3331739/ /pubmed/22517657 http://dx.doi.org/10.2337/db11-1511 Text en © 2012 by the American Diabetes Association. Readers may use this article as long as the work is properly cited, the use is educational and not for profit, and the work is not altered. See http://creativecommons.org/licenses/by-nc-nd/3.0/ for details. |
spellingShingle | Obesity Studies Visinoni, Sherley Khalid, Nurul Fathiah Izzati Joannides, Christos N. Shulkes, Arthur Yim, Mildred Whitehead, Jon Tiganis, Tony Lamont, Benjamin J. Favaloro, Jenny M. Proietto, Joseph Andrikopoulos, Sofianos Fam, Barbara C. The Role of Liver Fructose-1,6-Bisphosphatase in Regulating Appetite and Adiposity |
title | The Role of Liver Fructose-1,6-Bisphosphatase in Regulating Appetite and Adiposity |
title_full | The Role of Liver Fructose-1,6-Bisphosphatase in Regulating Appetite and Adiposity |
title_fullStr | The Role of Liver Fructose-1,6-Bisphosphatase in Regulating Appetite and Adiposity |
title_full_unstemmed | The Role of Liver Fructose-1,6-Bisphosphatase in Regulating Appetite and Adiposity |
title_short | The Role of Liver Fructose-1,6-Bisphosphatase in Regulating Appetite and Adiposity |
title_sort | role of liver fructose-1,6-bisphosphatase in regulating appetite and adiposity |
topic | Obesity Studies |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3331739/ https://www.ncbi.nlm.nih.gov/pubmed/22517657 http://dx.doi.org/10.2337/db11-1511 |
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