[HTML][HTML] Changes in dietary fat content rapidly alters the mouse plasma coagulation profile without affecting relative transcript levels of coagulation factors
ACA Cleuren, VT Blankevoort, JA van Diepen… - PLoS …, 2015 - journals.plos.org
ACA Cleuren, VT Blankevoort, JA van Diepen, D Verhoef, PJ Voshol, PH Reitsma…
PLoS One, 2015•journals.plos.orgBackground Obesity is associated with a hypercoagulable state and increased risk for
thrombotic cardiovascular events. Objective Establish the onset and reversibility of the
hypercoagulable state during the development and regression of nutritionally-induced
obesity in mice, and its relation to transcriptional changes and clearance rates of
coagulation factors as well as its relation to changes in metabolic and inflammatory
parameters. Methods Male C57BL/6J mice were fed a low fat (10% kcal as fat; LFD) or high …
thrombotic cardiovascular events. Objective Establish the onset and reversibility of the
hypercoagulable state during the development and regression of nutritionally-induced
obesity in mice, and its relation to transcriptional changes and clearance rates of
coagulation factors as well as its relation to changes in metabolic and inflammatory
parameters. Methods Male C57BL/6J mice were fed a low fat (10% kcal as fat; LFD) or high …
Background
Obesity is associated with a hypercoagulable state and increased risk for thrombotic cardiovascular events.
Objective
Establish the onset and reversibility of the hypercoagulable state during the development and regression of nutritionally-induced obesity in mice, and its relation to transcriptional changes and clearance rates of coagulation factors as well as its relation to changes in metabolic and inflammatory parameters.
Methods
Male C57BL/6J mice were fed a low fat (10% kcal as fat; LFD) or high fat diet (45% kcal as fat; HFD) for 2, 4, 8 or 16 weeks. To study the effects of weight loss, mice were fed the HFD for 16 weeks and switched to the LFD for 1, 2 or 4 weeks. For each time point analyses of plasma and hepatic mRNA levels of coagulation factors were performed after overnight fasting, as well as measurements of circulating metabolic and inflammatory parameters. Furthermore, in vivo clearance rates of human factor (F) VII, FVIII and FIX proteins were determined after 2 weeks of HFD-feeding.
Results
HFD feeding gradually increased the body and liver weight, which was accompanied by a significant increase in plasma glucose levels from 8 weeks onwards, while insulin levels were affected after 16 weeks. Besides a transient rise in cytokine levels at 2 weeks after starting the HFD, no significant effect on inflammation markers was present. Increased plasma levels of fibrinogen, FII, FVII, FVIII, FIX, FXI and FXII were observed in mice on a HFD for 2 weeks, which in general persisted throughout the 16 weeks of HFD-feeding. Interestingly, with the exception of FXI the effects on plasma coagulation levels were not paralleled by changes in relative transcript levels in the liver, nor by decreased clearance rates. Switching from HFD to LFD reversed the HFD-induced procoagulant shift in plasma, again not coinciding with transcriptional modulation.
Conclusions
Changes in dietary fat content rapidly alter the mouse plasma coagulation profile, thereby preceding plasma metabolic changes, which cannot be explained by changes in relative expression of coagulation factors or decreased clearance rates.
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