Comparative Study of Different Polar Groups of EPA-Enriched Phospholipids on Ameliorating Memory Loss and Cognitive Deficiency in Aged SAMP8 Mice

Mol Nutr Food Res. 2018 Apr;62(7):e1700637. doi: 10.1002/mnfr.201700637. Epub 2018 Mar 12.

Abstract

Scope: Recent studies have shown that omega-3 PUFAs enriched phospholipids (n-3 PUFA-PLs) have beneficial effects on memory and cognition. However, most reports only attribute the benefit to docosahexaenoic acid (DHA) and pay little attention to eicosapentaenoic acid (EPA).

Methods and results: We investigate the effect of EPA-enriched phospholipids on cognitive deficiency in senescence-accelerated prone 8 (SAMP8) mouse. Ten-month-old SAMP8 mice are fed with 2% (w/w) EPA-enriched phosphatidylcholine/phosphatidyl ethanolamine (EPA-PC/PE; EPA:DHA = 46.8:3.01) or 2% EPA-enriched phosphatidylserine (EPA-PS; biosynthesized from EPA-PC/PE) for 8 weeks; we then test the behavioral performances in the Barnes maze test and Morris maze test; the changes of oxidative stress, apoptosis, neurotrophic factors, tau phosphorylation, and Aβ pathology are also measured. The results of behavior tests indicate that both EPA-PC/PE and EPA-PS significantly improve memory and cognitive deficiency. It is found that remarkable amelioration of oxidative stress and apoptosis occurs in both EPA-PC/PE and EPA-PS groups. EPA-PS shows more ameliorative effects than EPA-PC/PE on neurotrophic activity by decreasing hyper-phosphorylation of tau and depressing the generation and accumulation of β-amyloid peptide (Aβ).

Conclusion: These data suggest that EPA-PS exhibits better effects than EPA-PC/PE on ameliorating memory and cognitive function, which might be attributed to the phospholipid polar groups.

Keywords: apoptosis; cognitive deficiency; marine food; phosphatidylserine; β-amyloid.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aging*
  • Animals
  • Apoptosis
  • Behavior, Animal
  • Brain / metabolism
  • Calceolariaceae / chemistry
  • Cognitive Dysfunction / prevention & control*
  • Dietary Supplements*
  • Eicosapentaenoic Acid / therapeutic use*
  • Gene Expression Regulation, Developmental
  • Male
  • Memory Disorders / prevention & control*
  • Mice
  • Mice, Mutant Strains
  • Nerve Tissue Proteins / genetics
  • Nerve Tissue Proteins / metabolism
  • Neurons / metabolism
  • Nootropic Agents / therapeutic use*
  • Oxidative Stress
  • Phosphatidylcholines / therapeutic use
  • Phosphatidylethanolamines / therapeutic use
  • Phosphatidylserines / therapeutic use
  • Phospholipids / therapeutic use*
  • Random Allocation

Substances

  • Nerve Tissue Proteins
  • Nootropic Agents
  • Phosphatidylcholines
  • Phosphatidylethanolamines
  • Phosphatidylserines
  • Phospholipids
  • Eicosapentaenoic Acid