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Concordance of Changes in Metabolic Pathways Based on Plasma Metabolomics and Skeletal Muscle Transcriptomics in Type 1 Diabetes

Insulin regulates many cellular processes, but the full impact of insulin deficiency on cellular functions remains to be defined. Applying a mass spectrometry–based nontargeted metabolomics approach, we report here alterations of 330 plasma metabolites representing 33 metabolic pathways during an 8-...

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Autores principales: Dutta, Tumpa, Chai, High Seng, Ward, Lawrence E., Ghosh, Aditya, Persson, Xuan-Mai T., Ford, G. Charles, Kudva, Yogish C., Sun, Zhifu, Asmann, Yan W., Kocher, Jean-Pierre A., Nair, K. Sreekumaran
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Diabetes Association 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3331761/
https://www.ncbi.nlm.nih.gov/pubmed/22415876
http://dx.doi.org/10.2337/db11-0874
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author Dutta, Tumpa
Chai, High Seng
Ward, Lawrence E.
Ghosh, Aditya
Persson, Xuan-Mai T.
Ford, G. Charles
Kudva, Yogish C.
Sun, Zhifu
Asmann, Yan W.
Kocher, Jean-Pierre A.
Nair, K. Sreekumaran
author_facet Dutta, Tumpa
Chai, High Seng
Ward, Lawrence E.
Ghosh, Aditya
Persson, Xuan-Mai T.
Ford, G. Charles
Kudva, Yogish C.
Sun, Zhifu
Asmann, Yan W.
Kocher, Jean-Pierre A.
Nair, K. Sreekumaran
author_sort Dutta, Tumpa
collection PubMed
description Insulin regulates many cellular processes, but the full impact of insulin deficiency on cellular functions remains to be defined. Applying a mass spectrometry–based nontargeted metabolomics approach, we report here alterations of 330 plasma metabolites representing 33 metabolic pathways during an 8-h insulin deprivation in type 1 diabetic individuals. These pathways included those known to be affected by insulin such as glucose, amino acid and lipid metabolism, Krebs cycle, and immune responses and those hitherto unknown to be altered including prostaglandin, arachidonic acid, leukotrienes, neurotransmitters, nucleotides, and anti-inflammatory responses. A significant concordance of metabolome and skeletal muscle transcriptome–based pathways supports an assumption that plasma metabolites are chemical fingerprints of cellular events. Although insulin treatment normalized plasma glucose and many other metabolites, there were 71 metabolites and 24 pathways that differed between nondiabetes and insulin-treated type 1 diabetes. Confirmation of many known pathways altered by insulin using a single blood test offers confidence in the current approach. Future research needs to be focused on newly discovered pathways affected by insulin deficiency and systemic insulin treatment to determine whether they contribute to the high morbidity and mortality in T1D despite insulin treatment.
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spelling pubmed-33317612013-05-01 Concordance of Changes in Metabolic Pathways Based on Plasma Metabolomics and Skeletal Muscle Transcriptomics in Type 1 Diabetes Dutta, Tumpa Chai, High Seng Ward, Lawrence E. Ghosh, Aditya Persson, Xuan-Mai T. Ford, G. Charles Kudva, Yogish C. Sun, Zhifu Asmann, Yan W. Kocher, Jean-Pierre A. Nair, K. Sreekumaran Diabetes Metabolism Insulin regulates many cellular processes, but the full impact of insulin deficiency on cellular functions remains to be defined. Applying a mass spectrometry–based nontargeted metabolomics approach, we report here alterations of 330 plasma metabolites representing 33 metabolic pathways during an 8-h insulin deprivation in type 1 diabetic individuals. These pathways included those known to be affected by insulin such as glucose, amino acid and lipid metabolism, Krebs cycle, and immune responses and those hitherto unknown to be altered including prostaglandin, arachidonic acid, leukotrienes, neurotransmitters, nucleotides, and anti-inflammatory responses. A significant concordance of metabolome and skeletal muscle transcriptome–based pathways supports an assumption that plasma metabolites are chemical fingerprints of cellular events. Although insulin treatment normalized plasma glucose and many other metabolites, there were 71 metabolites and 24 pathways that differed between nondiabetes and insulin-treated type 1 diabetes. Confirmation of many known pathways altered by insulin using a single blood test offers confidence in the current approach. Future research needs to be focused on newly discovered pathways affected by insulin deficiency and systemic insulin treatment to determine whether they contribute to the high morbidity and mortality in T1D despite insulin treatment. American Diabetes Association 2012-05 2012-04-13 /pmc/articles/PMC3331761/ /pubmed/22415876 http://dx.doi.org/10.2337/db11-0874 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 Metabolism
Dutta, Tumpa
Chai, High Seng
Ward, Lawrence E.
Ghosh, Aditya
Persson, Xuan-Mai T.
Ford, G. Charles
Kudva, Yogish C.
Sun, Zhifu
Asmann, Yan W.
Kocher, Jean-Pierre A.
Nair, K. Sreekumaran
Concordance of Changes in Metabolic Pathways Based on Plasma Metabolomics and Skeletal Muscle Transcriptomics in Type 1 Diabetes
title Concordance of Changes in Metabolic Pathways Based on Plasma Metabolomics and Skeletal Muscle Transcriptomics in Type 1 Diabetes
title_full Concordance of Changes in Metabolic Pathways Based on Plasma Metabolomics and Skeletal Muscle Transcriptomics in Type 1 Diabetes
title_fullStr Concordance of Changes in Metabolic Pathways Based on Plasma Metabolomics and Skeletal Muscle Transcriptomics in Type 1 Diabetes
title_full_unstemmed Concordance of Changes in Metabolic Pathways Based on Plasma Metabolomics and Skeletal Muscle Transcriptomics in Type 1 Diabetes
title_short Concordance of Changes in Metabolic Pathways Based on Plasma Metabolomics and Skeletal Muscle Transcriptomics in Type 1 Diabetes
title_sort concordance of changes in metabolic pathways based on plasma metabolomics and skeletal muscle transcriptomics in type 1 diabetes
topic Metabolism
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3331761/
https://www.ncbi.nlm.nih.gov/pubmed/22415876
http://dx.doi.org/10.2337/db11-0874
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