Addition of aspirin to a fish oil-rich diet decreases inflammation and atherosclerosis in ApoE-null mice

J Nutr Biochem. 2016 Sep:35:58-65. doi: 10.1016/j.jnutbio.2016.05.012. Epub 2016 Jun 19.

Abstract

Aspirin (ASA) is known to alter the production of potent inflammatory lipid mediators, but whether it interacts with omega-3 fatty acids (FAs) from fish oil to affect atherosclerosis has not been determined. The goal was to investigate the impact of a fish oil-enriched diet alone and in combination with ASA on the production of lipid mediators and atherosclerosis. ApoE(-/-) female mice were fed for 13weeks one of the four following diets: omega-3 FA deficient (OD), omega-3 FA rich (OR) (1.8g omega-3 FAs/kg·diet per day), omega-3 FA rich plus ASA (ORA) (0.1g ASA/kg·diet per day) or an omega-3 FA deficient plus ASA (ODA) with supplement levels equivalent to human doses. Plasma lipids, atherosclerosis, markers of inflammation, hepatic gene expression and aortic lipid mediators were determined. Hepatic omega-3 FAs were markedly higher in OR (9.9-fold) and ORA (7-fold) groups. Mice in both OR and ORA groups had 40% less plasma cholesterol in very low-density lipoprotein-cholesterol and low-density lipoprotein fractions, but aortic plaque area formation was only significantly lower in the ORA group (5.5%) compared to the OD group (2.5%). Plasma PCSK9 protein levels were approximately 70% lower in the OR and ORA groups. Proinflammatory aortic lipid mediators were 50%-70% lower in the ODA group than in the OD group and more than 50% lower in the ORA group. In summary, less aortic plaque lesions and aortic proinflammatory lipid mediators were observed in mice on the fish oil diet plus ASA vs. just the fish oil diet.

Keywords: Aspirin; Atherosclerosis; Fish oil; Inflammation; Omega-3 fatty acids.

Publication types

  • Comparative Study
  • Research Support, N.I.H., Extramural
  • Research Support, N.I.H., Intramural

MeSH terms

  • Animals
  • Anti-Inflammatory Agents, Non-Steroidal / adverse effects
  • Anti-Inflammatory Agents, Non-Steroidal / therapeutic use*
  • Aorta / drug effects*
  • Aorta / immunology
  • Aorta / metabolism
  • Aorta / pathology
  • Apolipoproteins E / genetics
  • Apolipoproteins E / metabolism
  • Aspirin / adverse effects
  • Aspirin / therapeutic use*
  • Atherosclerosis / immunology
  • Atherosclerosis / metabolism
  • Atherosclerosis / pathology
  • Atherosclerosis / prevention & control*
  • Biomarkers / blood
  • Biomarkers / metabolism
  • Cell Proliferation / drug effects
  • Endothelial Progenitor Cells / drug effects*
  • Endothelial Progenitor Cells / immunology
  • Endothelial Progenitor Cells / metabolism
  • Endothelial Progenitor Cells / pathology
  • Fatty Acids, Omega-3 / adverse effects
  • Fatty Acids, Omega-3 / blood
  • Fatty Acids, Omega-3 / metabolism
  • Fatty Acids, Omega-3 / therapeutic use
  • Female
  • Fish Oils / adverse effects
  • Fish Oils / metabolism
  • Fish Oils / therapeutic use*
  • Gene Expression Regulation / drug effects
  • Inflammation Mediators / blood
  • Lipid Metabolism / drug effects
  • Lipids / blood
  • Liver / drug effects*
  • Liver / immunology
  • Liver / metabolism
  • Liver / pathology
  • Mice, Knockout
  • Proprotein Convertase 9 / blood
  • Random Allocation
  • Weight Gain / drug effects

Substances

  • Anti-Inflammatory Agents, Non-Steroidal
  • Apolipoproteins E
  • Biomarkers
  • Fatty Acids, Omega-3
  • Fish Oils
  • Inflammation Mediators
  • Lipids
  • Pcsk9 protein, mouse
  • Proprotein Convertase 9
  • Aspirin