4.7 Article

Eicosapentaenoic acid in the form of phospholipids exerts superior anti-atherosclerosis effects to its triglyceride form in ApoE-/- mice

Journal

FOOD & FUNCTION
Volume 10, Issue 7, Pages 4177-4188

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c9fo00868c

Keywords

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Funding

  1. National Key R&D Program of China [2018YFD0901103]
  2. Natural Science Youth Foundation of Shandong Province [ZR2019QC004]
  3. China Postdoctoral Science Foundation [2017M620294]
  4. National Natural Science Foundation of China-Shandong Joint Fund for Marine Science Research Centers [U1606403]
  5. Fundamental Research Funds for the Central Universities [201762028, 201812017]
  6. Laboratory for Marine Drugs and Bioproducts of Pilot National Laboratory for Marine Science and Technology (Qingdao) [LMDBKF201807]
  7. Qingdao Postdoctoral Application Foundation

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Dietary eicosapentaenoic acid (EPA), a main component of fish oil, has been proved to reduce the risk of cardiovascular disease. The purpose of this study was to investigate whether the anti-atherosclerosis effect of fish oil enriched with EPA partially relied on its chemical groups at the sn-3 position. Male ApoE(-/-) mice were divided into three groups and were fed a high-fat diet (Model) or a high-fat diet containing EPA incorporated into phospholipids (EPA-PL) or triglycerides (EPA-TG), respectively. Compared with the model group, a decrease in the area of atherosclerosis lesions at the aorta was observed in both EPA-treated groups, in which EPA-PL was superior to EPA-TG. Notably, EPA-PL exhibited lower serum and hepatic lipid levels than the model group, whereas EPA-TG only reduced the hepatic triglyceride level. Interestingly, only EPA-PL treatment regulated the expression of genes involved in cholesterol metabolism. In addition, EPA-PL and EPA-TG suppressed the inflammation markers in the aorta and circulation. In conclusion, EPA-PL was superior to EPA-TG in reducing lesion progression by modulating the hepatic lipid metabolism, as well as decreasing the inflammation in the artery wall and circulatory system, which might be attributed to their structural differences at the sn-3 position.

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