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Altered Metabolic Signature in Pre-Diabetic NOD Mice

Altered metabolism proceeding seroconversion in children progressing to Type 1 diabetes has previously been demonstrated. We tested the hypothesis that non-obese diabetic (NOD) mice show a similarly altered metabolic profile compared to C57BL/6 mice. Blood samples from NOD and C57BL/6 female mice wa...

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Autores principales: Madsen, Rasmus, Banday, Viqar Showkat, Moritz, Thomas, Trygg, Johan, Lejon, Kristina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3326011/
https://www.ncbi.nlm.nih.gov/pubmed/22514744
http://dx.doi.org/10.1371/journal.pone.0035445
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author Madsen, Rasmus
Banday, Viqar Showkat
Moritz, Thomas
Trygg, Johan
Lejon, Kristina
author_facet Madsen, Rasmus
Banday, Viqar Showkat
Moritz, Thomas
Trygg, Johan
Lejon, Kristina
author_sort Madsen, Rasmus
collection PubMed
description Altered metabolism proceeding seroconversion in children progressing to Type 1 diabetes has previously been demonstrated. We tested the hypothesis that non-obese diabetic (NOD) mice show a similarly altered metabolic profile compared to C57BL/6 mice. Blood samples from NOD and C57BL/6 female mice was collected at 0, 1, 2, 3, 4, 5, 6, 7, 9, 11, 13 and 15 weeks and the metabolite content was analyzed using GC-MS. Based on the data of 89 identified metabolites OPLS-DA analysis was employed to determine the most discriminative metabolites. In silico analysis of potential involved metabolic enzymes was performed using the dbSNP data base. Already at 0 weeks NOD mice displayed a unique metabolic signature compared to C57BL/6. A shift in the metabolism was observed for both strains the first weeks of life, a pattern that stabilized after 5 weeks of age. Multivariate analysis revealed the most discriminative metabolites, which included inosine and glutamic acid. In silico analysis of the genes in the involved metabolic pathways revealed several SNPs in either regulatory or coding regions, some in previously defined insulin dependent diabetes (Idd) regions. Our result shows that NOD mice display an altered metabolic profile that is partly resembling the previously observation made in children progressing to Type 1 diabetes. The level of glutamic acid was one of the most discriminative metabolites in addition to several metabolites in the TCA cycle and nucleic acid components. The in silico analysis indicated that the genes responsible for this reside within previously defined Idd regions.
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spelling pubmed-33260112012-04-18 Altered Metabolic Signature in Pre-Diabetic NOD Mice Madsen, Rasmus Banday, Viqar Showkat Moritz, Thomas Trygg, Johan Lejon, Kristina PLoS One Research Article Altered metabolism proceeding seroconversion in children progressing to Type 1 diabetes has previously been demonstrated. We tested the hypothesis that non-obese diabetic (NOD) mice show a similarly altered metabolic profile compared to C57BL/6 mice. Blood samples from NOD and C57BL/6 female mice was collected at 0, 1, 2, 3, 4, 5, 6, 7, 9, 11, 13 and 15 weeks and the metabolite content was analyzed using GC-MS. Based on the data of 89 identified metabolites OPLS-DA analysis was employed to determine the most discriminative metabolites. In silico analysis of potential involved metabolic enzymes was performed using the dbSNP data base. Already at 0 weeks NOD mice displayed a unique metabolic signature compared to C57BL/6. A shift in the metabolism was observed for both strains the first weeks of life, a pattern that stabilized after 5 weeks of age. Multivariate analysis revealed the most discriminative metabolites, which included inosine and glutamic acid. In silico analysis of the genes in the involved metabolic pathways revealed several SNPs in either regulatory or coding regions, some in previously defined insulin dependent diabetes (Idd) regions. Our result shows that NOD mice display an altered metabolic profile that is partly resembling the previously observation made in children progressing to Type 1 diabetes. The level of glutamic acid was one of the most discriminative metabolites in addition to several metabolites in the TCA cycle and nucleic acid components. The in silico analysis indicated that the genes responsible for this reside within previously defined Idd regions. Public Library of Science 2012-04-13 /pmc/articles/PMC3326011/ /pubmed/22514744 http://dx.doi.org/10.1371/journal.pone.0035445 Text en Madsen 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, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Madsen, Rasmus
Banday, Viqar Showkat
Moritz, Thomas
Trygg, Johan
Lejon, Kristina
Altered Metabolic Signature in Pre-Diabetic NOD Mice
title Altered Metabolic Signature in Pre-Diabetic NOD Mice
title_full Altered Metabolic Signature in Pre-Diabetic NOD Mice
title_fullStr Altered Metabolic Signature in Pre-Diabetic NOD Mice
title_full_unstemmed Altered Metabolic Signature in Pre-Diabetic NOD Mice
title_short Altered Metabolic Signature in Pre-Diabetic NOD Mice
title_sort altered metabolic signature in pre-diabetic nod mice
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3326011/
https://www.ncbi.nlm.nih.gov/pubmed/22514744
http://dx.doi.org/10.1371/journal.pone.0035445
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