A comparative study of eicosapentaenoic acid enriched phosphatidylcholine and ethyl ester in improving cognitive deficiency in Alzheimer's disease model rats

Food Funct. 2018 Apr 25;9(4):2184-2192. doi: 10.1039/c7fo01815k.

Abstract

Abundant studies have highlighted the protective effects of docosahexaenoic acid (DHA), in the form of glycerolipids (glycerophosphatides and triglycerides) and DHA-ethyl esters (DHA-EE) in Alzheimer's disease (AD); however, eicosapentaenoic acid (EPA) has rarely been implicated. In the present study, we compared the effects of dietary EPA in the form of phosphatidylcholine (EPA-PC) and EE with DHA-EE (DHA/EPA = 60 mg kg-1 d-1, i.g., 20 days) on cognitive deficits in AD rats. EPA-PC, rather than EPA-EE, significantly improved Aβ-induced cognitive impairment and has a comparable effect with DHA-EE. Further research indicated that EPA-PC and DHA-EE could significantly decrease lipid peroxidation levels, alleviate mitochondria-dependent apoptosis, and inhibit the hyperphosphorylation of tau mediated by GSK3β. These findings suggest that EPA in the form of phosphatidylcholine rather than an ethyl ester has a comparable effect with DHA in improving cognitive impairment in Aβ1-42-induced AD rats.

Publication types

  • Comparative Study

MeSH terms

  • Alkylation
  • Alzheimer Disease / metabolism
  • Alzheimer Disease / prevention & control*
  • Animals
  • Apoptosis
  • Behavior, Animal
  • Cerebral Cortex / metabolism
  • Dietary Supplements*
  • Disease Models, Animal*
  • Docosahexaenoic Acids / analogs & derivatives
  • Docosahexaenoic Acids / therapeutic use
  • Eicosapentaenoic Acid / analogs & derivatives
  • Eicosapentaenoic Acid / therapeutic use*
  • Glycogen Synthase Kinase 3 beta / metabolism
  • Male
  • Maze Learning
  • Neurons / metabolism
  • Nootropic Agents / therapeutic use*
  • Oxidative Stress*
  • Phosphatidylcholines / therapeutic use*
  • Phosphorylation
  • Protein Processing, Post-Translational
  • Random Allocation
  • Rats, Sprague-Dawley
  • tau Proteins / metabolism

Substances

  • Mapt protein, rat
  • Nootropic Agents
  • Phosphatidylcholines
  • tau Proteins
  • Docosahexaenoic Acids
  • Eicosapentaenoic Acid
  • Glycogen Synthase Kinase 3 beta
  • Gsk3b protein, rat