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Longitudinal analysis of hepatic transcriptome and serum metabolome demonstrates altered lipid metabolism following the onset of hyperglycemia in spontaneously diabetic biobreeding rats

Type 1 diabetes is associated with abberations of fat metabolism before and after the clinical onset of disease. It has been hypothesized that the absence of the effect of insulin in the liver contributes to reduced hepatic fat synthesis. We measured hepatic gene expression and serum metabolites bef...

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Autores principales: Regnell, Simon E., Hessner, Martin J., Jia, Shuang, Åkesson, Lina, Stenlund, Hans, Moritz, Thomas, La Torre, Daria, Lernmark, Åke
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5305198/
https://www.ncbi.nlm.nih.gov/pubmed/28192442
http://dx.doi.org/10.1371/journal.pone.0171372
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author Regnell, Simon E.
Hessner, Martin J.
Jia, Shuang
Åkesson, Lina
Stenlund, Hans
Moritz, Thomas
La Torre, Daria
Lernmark, Åke
author_facet Regnell, Simon E.
Hessner, Martin J.
Jia, Shuang
Åkesson, Lina
Stenlund, Hans
Moritz, Thomas
La Torre, Daria
Lernmark, Åke
author_sort Regnell, Simon E.
collection PubMed
description Type 1 diabetes is associated with abberations of fat metabolism before and after the clinical onset of disease. It has been hypothesized that the absence of the effect of insulin in the liver contributes to reduced hepatic fat synthesis. We measured hepatic gene expression and serum metabolites before and after the onset of hyperglycemia in a BioBreeding rat model of type 1 diabetes. Functional pathway annotation identified that lipid metabolism was differentially expressed in hyperglycemic rats and that these pathways significantly overlapped with genes regulated by insulin. 17 serum metabolites significantly changed in concentration. All but 2 of the identified metabolites had previously been reported in type 1 diabetes, and carbohydrates were overall the most upregulated class of metabolites. We conclude that lack of insulin in the liver contributes to the changes in fat metabolism observed in type 1 diabetes. Further studies are needed to understand the clinical consequences of a lack of insulin in the liver in patients with type 1 diabetes.
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spelling pubmed-53051982017-02-28 Longitudinal analysis of hepatic transcriptome and serum metabolome demonstrates altered lipid metabolism following the onset of hyperglycemia in spontaneously diabetic biobreeding rats Regnell, Simon E. Hessner, Martin J. Jia, Shuang Åkesson, Lina Stenlund, Hans Moritz, Thomas La Torre, Daria Lernmark, Åke PLoS One Research Article Type 1 diabetes is associated with abberations of fat metabolism before and after the clinical onset of disease. It has been hypothesized that the absence of the effect of insulin in the liver contributes to reduced hepatic fat synthesis. We measured hepatic gene expression and serum metabolites before and after the onset of hyperglycemia in a BioBreeding rat model of type 1 diabetes. Functional pathway annotation identified that lipid metabolism was differentially expressed in hyperglycemic rats and that these pathways significantly overlapped with genes regulated by insulin. 17 serum metabolites significantly changed in concentration. All but 2 of the identified metabolites had previously been reported in type 1 diabetes, and carbohydrates were overall the most upregulated class of metabolites. We conclude that lack of insulin in the liver contributes to the changes in fat metabolism observed in type 1 diabetes. Further studies are needed to understand the clinical consequences of a lack of insulin in the liver in patients with type 1 diabetes. Public Library of Science 2017-02-13 /pmc/articles/PMC5305198/ /pubmed/28192442 http://dx.doi.org/10.1371/journal.pone.0171372 Text en © 2017 Regnell et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Regnell, Simon E.
Hessner, Martin J.
Jia, Shuang
Åkesson, Lina
Stenlund, Hans
Moritz, Thomas
La Torre, Daria
Lernmark, Åke
Longitudinal analysis of hepatic transcriptome and serum metabolome demonstrates altered lipid metabolism following the onset of hyperglycemia in spontaneously diabetic biobreeding rats
title Longitudinal analysis of hepatic transcriptome and serum metabolome demonstrates altered lipid metabolism following the onset of hyperglycemia in spontaneously diabetic biobreeding rats
title_full Longitudinal analysis of hepatic transcriptome and serum metabolome demonstrates altered lipid metabolism following the onset of hyperglycemia in spontaneously diabetic biobreeding rats
title_fullStr Longitudinal analysis of hepatic transcriptome and serum metabolome demonstrates altered lipid metabolism following the onset of hyperglycemia in spontaneously diabetic biobreeding rats
title_full_unstemmed Longitudinal analysis of hepatic transcriptome and serum metabolome demonstrates altered lipid metabolism following the onset of hyperglycemia in spontaneously diabetic biobreeding rats
title_short Longitudinal analysis of hepatic transcriptome and serum metabolome demonstrates altered lipid metabolism following the onset of hyperglycemia in spontaneously diabetic biobreeding rats
title_sort longitudinal analysis of hepatic transcriptome and serum metabolome demonstrates altered lipid metabolism following the onset of hyperglycemia in spontaneously diabetic biobreeding rats
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5305198/
https://www.ncbi.nlm.nih.gov/pubmed/28192442
http://dx.doi.org/10.1371/journal.pone.0171372
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