Open AccessInteraction between plasma fetuin‐A and free fatty acids predicts changes in insulin sensitivity in response to long‐term exercise
Author(s) -
Lee Sindre,
Norheim Frode,
Gulseth Hanne L.,
Langleite Torgrim M.,
Kolnes Kristoffer J.,
Tangen Daniel S.,
Stadheim Hans K.,
Gilfillan Gregor D.,
Holen Torgeir,
Birkeland Kåre I.,
Jensen Jørgen,
Drevon Christian A.
Publication year - 2017
Publication title -
physiological reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.918
H-Index - 39
ISSN - 2051-817X
DOI - 10.14814/phy2.13183
Subject(s) - medicine , endocrinology , insulin resistance , fetuin , glucose clamp technique , insulin , adipose tissue , myokine , skeletal muscle , inflammation , glucose uptake , insulin sensitivity , type 2 diabetes , chemistry , diabetes mellitus , biochemistry , glycoprotein
The hepatokine fetuin‐A can together with free fatty acids ( FFA s) enhance adipose tissue ( AT ) inflammation and insulin resistance via toll‐like receptor 4 ( TLR 4). Although some of the health benefits of exercise can be explained by altered release of myokines from the skeletal muscle, it is not well documented if some of the beneficial effects of exercise can be explained by altered secretion of hepatokines. The aim of this study was to examine the effect of interaction between fetuin‐A and FFA s on insulin sensitivity after physical exercise. In this study, 26 sedentary men who underwent 12 weeks of combined endurance and strength exercise were included. Insulin sensitivity was measured using euglycemic‐hyperinsulinemic clamp, and AT insulin resistance was indicated by the product of fasting plasma concentration of FFA s and insulin. Blood samples and biopsies from skeletal muscle and subcutaneous AT were collected. Several phenotypic markers were measured, and mRNA sequencing was performed on the biopsies. AT macrophages were analyzed based on mRNA markers. The intervention improved hepatic parameters, reduced plasma fetuin‐A concentration (~11%, P < 0.01), slightly changed FFA s concentration, and improved glucose infusion rate ( GIR ) (~33%, P < 0.01) across all participants. The change in circulating fetuin‐A and FFA s interacted to predict some of the change in GIR ( β = −42.16, P = 0.030), AT insulin resistance ( β = 0.579, P = 0.003), gene expression related to TLR ‐signaling in AT and AT macrophage mRNA ( β = 94.10, P = 0.034) after exercise. We observed no interaction effects between FFA s concentrations and leptin and adiponectin on insulin sensitivity, or any interaction effects between Fetuin‐A and FFA s concentrations on skeletal muscle TLR ‐signaling. The relationship between FFAs levels and insulin sensitivity seemed to be specific for fetuin‐A and the AT . Some of the beneficial effects of exercise on insulin sensitivity may be explained by changes in circulating fetuin‐A and FFA s, promoting less TLR 4 signaling in AT perhaps by modulating AT macrophages.