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Insulin resistance is associated with altered amino acid metabolism and adipose tissue dysfunction in normoglycemic women
Insulin resistance is associated adiposity, but the mechanisms are not fully understood. In this study, we aimed to identify early metabolic alterations associated with insulin resistance in normoglycemic women with varying degree of adiposity. One-hundred and ten young and middle-aged women were di...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4832240/ https://www.ncbi.nlm.nih.gov/pubmed/27080554 http://dx.doi.org/10.1038/srep24540 |
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author | Wiklund, Petri Zhang, Xiaobo Pekkala, Satu Autio, Reija Kong, Lingjia Yang, Yifan Keinänen-Kiukaanniemi, Sirkka Alen, Markku Cheng, Sulin |
author_facet | Wiklund, Petri Zhang, Xiaobo Pekkala, Satu Autio, Reija Kong, Lingjia Yang, Yifan Keinänen-Kiukaanniemi, Sirkka Alen, Markku Cheng, Sulin |
author_sort | Wiklund, Petri |
collection | PubMed |
description | Insulin resistance is associated adiposity, but the mechanisms are not fully understood. In this study, we aimed to identify early metabolic alterations associated with insulin resistance in normoglycemic women with varying degree of adiposity. One-hundred and ten young and middle-aged women were divided into low and high IR groups based on their median HOMA-IR (0.9 ± 0.4 vs. 2.8 ± 1.2). Body composition was assessed using DXA, skeletal muscle and liver fat by proton magnetic resonance spectroscopy, serum metabolites by nuclear magnetic resonance spectroscopy and adipose tissue and skeletal muscle gene expression by microarrays. High HOMA-IR subjects had higher serum branched-chain amino acid concentrations (BCAA) (p < 0.05 for both). Gene expression analysis of subcutaneous adipose tissue revealed significant down-regulation of genes related to BCAA catabolism and mitochondrial energy metabolism and up-regulation of several inflammation-related pathways in high HOMA-IR subjects (p < 0.05 for all), but no differentially expressed genes in skeletal muscle were found. In conclusion, in normoglycemic women insulin resistance was associated with increased serum BCAA concentrations, down-regulation of mitochondrial energy metabolism and increased expression of inflammation-related genes in the adipose tissue. |
format | Online Article Text |
id | pubmed-4832240 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-48322402016-04-20 Insulin resistance is associated with altered amino acid metabolism and adipose tissue dysfunction in normoglycemic women Wiklund, Petri Zhang, Xiaobo Pekkala, Satu Autio, Reija Kong, Lingjia Yang, Yifan Keinänen-Kiukaanniemi, Sirkka Alen, Markku Cheng, Sulin Sci Rep Article Insulin resistance is associated adiposity, but the mechanisms are not fully understood. In this study, we aimed to identify early metabolic alterations associated with insulin resistance in normoglycemic women with varying degree of adiposity. One-hundred and ten young and middle-aged women were divided into low and high IR groups based on their median HOMA-IR (0.9 ± 0.4 vs. 2.8 ± 1.2). Body composition was assessed using DXA, skeletal muscle and liver fat by proton magnetic resonance spectroscopy, serum metabolites by nuclear magnetic resonance spectroscopy and adipose tissue and skeletal muscle gene expression by microarrays. High HOMA-IR subjects had higher serum branched-chain amino acid concentrations (BCAA) (p < 0.05 for both). Gene expression analysis of subcutaneous adipose tissue revealed significant down-regulation of genes related to BCAA catabolism and mitochondrial energy metabolism and up-regulation of several inflammation-related pathways in high HOMA-IR subjects (p < 0.05 for all), but no differentially expressed genes in skeletal muscle were found. In conclusion, in normoglycemic women insulin resistance was associated with increased serum BCAA concentrations, down-regulation of mitochondrial energy metabolism and increased expression of inflammation-related genes in the adipose tissue. Nature Publishing Group 2016-04-15 /pmc/articles/PMC4832240/ /pubmed/27080554 http://dx.doi.org/10.1038/srep24540 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Wiklund, Petri Zhang, Xiaobo Pekkala, Satu Autio, Reija Kong, Lingjia Yang, Yifan Keinänen-Kiukaanniemi, Sirkka Alen, Markku Cheng, Sulin Insulin resistance is associated with altered amino acid metabolism and adipose tissue dysfunction in normoglycemic women |
title | Insulin resistance is associated with altered amino acid metabolism and adipose tissue dysfunction in normoglycemic women |
title_full | Insulin resistance is associated with altered amino acid metabolism and adipose tissue dysfunction in normoglycemic women |
title_fullStr | Insulin resistance is associated with altered amino acid metabolism and adipose tissue dysfunction in normoglycemic women |
title_full_unstemmed | Insulin resistance is associated with altered amino acid metabolism and adipose tissue dysfunction in normoglycemic women |
title_short | Insulin resistance is associated with altered amino acid metabolism and adipose tissue dysfunction in normoglycemic women |
title_sort | insulin resistance is associated with altered amino acid metabolism and adipose tissue dysfunction in normoglycemic women |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4832240/ https://www.ncbi.nlm.nih.gov/pubmed/27080554 http://dx.doi.org/10.1038/srep24540 |
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