Journal
JOURNAL OF NUTRITIONAL BIOCHEMISTRY
Volume 25, Issue 5, Pages 573-579Publisher
ELSEVIER SCIENCE INC
DOI: 10.1016/j.jnutbio.2014.01.008
Keywords
Atorvastatin; CD36; Fatty acid translocase; Hepatic fatty acid uptake; High-fat diet; Scavenger receptor; Steatosis; Tocopherol; Vitamin E
Funding
- DSM Nutritional Products (Kaiseraugst, Switzerland)
- German Research Foundation (DFG) [2478/4-1]
- Ina Bergheim
- German Federal Ministry of Education and Research (BMBF) [03105084]
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The increased uptake and storage of lipids in the liver are important features of steatotic liver diseases. The fatty acid translocase/scavenger receptor cluster of differentiation (CD)36 facilitates the hepatic uptake of lipids. We investigated if RRR-alpha-tocopherol (alpha T) alone or in combination with atorvastatin (ATV) is capable of preventing hepatic lipid accumulation via down-regulation of CD36. To this end, Dunkin Hartley guinea pigs were fed a control diet (5% fat); or a high-fat control diet (21% fat, 0.15% cholesterol); or a high-fat control diet fortified with aT (250 mg/kg diet), ATV (300 mg/kg diet) or both ATV+alpha T for 6 weeks. Hepatic triacylglycerols, hepatic protein and mRNA expression of CD36 as well as the mRNA expression of the controlling nuclear receptors LXR alpha, PXR and PPAR gamma were determined. Animals fed the high-fat control diet accumulated significantly more triacylglycerols in the liver than control animals. This was significantly reduced by ATV and numerically by alpha T and ATV+alpha T. Hepatic CD36 protein concentrations were significantly higher in the high-fat than in the control group, and both alpha T and ATV reduced CD36 expression to the level observed in the control group. However, no synergistic effect of the combined treatment was observed. Neither CD36 mRNA nor that of the nuclear receptors (LXR alpha, PXR and PPAR gamma) differed between groups, suggesting a posttranslational regulatory mechanism. Our results indicate that orally administered ATV and aT individually, but not synergistically, prevent diet-induced lipid accumulation in the liver of guinea pigs by down-regulation of hepatic CD36 protein. (C) 2014 Elsevier Inc. All rights reserved.
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