Increase in skeletal muscle fatty acid binding protein (FABPC) content is directly related to weight loss and to changes in fat oxidation following avery low calorie diet
Ee. Blaak et al., Increase in skeletal muscle fatty acid binding protein (FABPC) content is directly related to weight loss and to changes in fat oxidation following avery low calorie diet, DIABETOLOG, 44(11), 2001, pp. 2013-2017
Aims/hypothesis. There is increasing evidence that intracellular fatty acid
binding proteins (FABPc's; 15 kD) function as vehicles of cytosolic fatty
acid transport. We studied skeletal muscle cytosolic FABPc, and enzymes ref
lecting beta -oxidation and oxidative capacity (3-hydroxyacyl-CoA dehydroge
nase, HAD, and citrate synthase, CS) in relation to weight loss and changes
in substrate utilisation in a group of 35 obese women and obese men with T
ype II (non-insulin-dependent) diabetes mellitus (women = 27, men = 8).
Methods. Muscle biopsies (vastus lateralis), and measurements of body compo
sition, resting energy expenditure and respiratory exchange ratio were take
n before and after dietary intervention (by means of a very low calorie die
t).
Results. Muscle FABPc tended to increase after diet (178 +/- 13 vs 204 +/-
12 mg.gww(-1), p = 0.06), whereas there were no changes in CS (10.5 +/- 0.7
vs 11.1 +/- 0.6 U.gww(-1)) and HAD (11.2+/-0.7 vs 11.7+/-0.6 U.gww(-1)). T
here was a positive relation between the increase in FABPc as result of die
t and the amount of weight lost (p < 0.01; adjusted R-2, 15.4%). even when
adjusted for mean body weight, and changes in CS and in HAD by partial regr
ession analysis. Interestingly, the increase in FABPc was positively relate
d to increases in resting fat oxidation (adjusted R-2, 24%), even when adju
sted for mean resting fat oxidation, and changes in CS and in HAD.
Conclusion/interpretation. In conclusion, the ability to increase muscle FA
BPc could be directly related to weight loss and to changes in fat oxidatio
n following dietary intervention in obesity and Type II (noninsulin-depende
nt) diabetes mellitus.