Antioxidant system response is modified by dietary fat in adipose tissue of metabolic syndrome patients

Metabolic Syndrome 0301 basic medicine 2. Zero hunger Glutathione Peroxidase Membrane Glycoproteins NF-E2-Related Factor 2 NADPH Oxidases Middle Aged Catalase Phosphoproteins Postprandial Period Dietary Fats Antioxidants 3. Good health Fatty Acids, Monounsaturated Oxidative Stress 03 medical and health sciences Adipose Tissue Dietary Fats, Unsaturated Fatty Acids, Omega-3 NADPH Oxidase 2 Humans RNA, Messenger
DOI: 10.1016/j.jnutbio.2013.02.012 Publication Date: 2013-05-03T09:42:19Z
ABSTRACT
Metabolic syndrome (MetS) is associated with high oxidative stress, which is caused by an increased expression of NADPH-oxidase and a decreased expression of antioxidant enzymes in the adipose tissue. Our aim was to evaluate whether the quality and quantity of dietary fat can modify that process. A randomized, controlled trial conducted within the LIPGENE study assigned MetS patients to one of four diets for 12 wk each: (i) high-saturated fatty acid (HSFA), (ii) high-monounsaturated fatty acid (HMUFA), (iii) and (iv) two low-fat, high-complex carbohydrate diet supplemented with n-3 polyunsaturated fatty acids (LFHCC n3), or placebo (LFHCC). A fat challenge reflecting the same fatty acid composition as the original diets was conducted post-intervention. The intake of an HSFA meal induced a higher postprandial increase in gp91phox and p67phox mRNA levels than after the intake of HMUFA, LFHCC and LFHCC n-3 meals (all p-values<0.05). The postprandial decrease in CAT, GPXs and TXNRD1 mRNA levels after the HSFA meal intake was higher than after the intake of HMUFA, LFHCC and LFHCC n-3 meals (all p-values<0.05). The intake of an HSFA meal induced a higher postprandial increase in KEAP1 mRNA levels than after the consumption of the HMUFA (P=.007) and LFHCC n-3 (P=.001) meals. Our study demonstrated that monounsaturated fat consumption reduces oxidative stress as compared to saturated fat by inducing higher postprandial antioxidant response in adipose tissue, and thus, replacing SFA for MUFA may be an effective dietary strategy to reduce the oxidative stress in MetS patients and its pathophysiological consequences.
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