Insulin resistance is associated with altered amino acid metabolism and adipose tissue dysfunction in normoglycemic women
Wiklund, P., Zhang, X., Pekkala, S., Autio, R., Kong, L., Yang, Y., Keinänen-Kiukaanniemi, S., Alen, M., & Cheng, S. (2016). Insulin resistance is associated with altered amino acid metabolism and adipose tissue dysfunction in normoglycemic women. Scientific Reports, 6, Article 24540. https://doi.org/10.1038/srep24540
Julkaistu sarjassa
Scientific ReportsTekijät
Päivämäärä
2016Tekijänoikeudet
© the Authors, 2016. This is an open access article published by Nature Publishing Group and distributed under a Creative Commons Attribution 4.0 International License.
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.
...
Julkaisija
Nature Publishing GroupISSN Hae Julkaisufoorumista
2045-2322Julkaisu tutkimustietojärjestelmässä
https://converis.jyu.fi/converis/portal/detail/Publication/25693571
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