Endogenous Docosahexaenoic Acid (DHA) Prevents Aβ1-42 Oligomer-Induced Neuronal Injury

Mol Neurobiol. 2016 Jul;53(5):3146-3153. doi: 10.1007/s12035-015-9224-0. Epub 2015 May 30.

Abstract

The intake of the polyunsaturated fatty acid docosahexaenoic acid (DHA) or n-3 fatty acid has been associated with reduced risk of Alzheimer's disease (AD) in epidemiological reports. However, the underlying mechanism remains to be elucidated. Here, we report that exogenous DHA administration could protect neurons against Aβ oligomer-induced injury both in vitro and in vivo, partly through reducing the endoplasmic reticulum (ER) stress, and preventing cell apoptosis. In transgenic fat-1 mice with enriched ω-3 fatty acids, Aβ oligomers induced fewer neuronal losses, when compared to wild-type (WT) mice. We conclude that endogenous DHA are neuroprotective in pathogenesis processes of AD.

Keywords: Alzheimer’s disease; Aβ oligomers; DHA; Fat-1 mice; Omega-3.

MeSH terms

  • Amyloid beta-Peptides / toxicity*
  • Animals
  • Apoptosis / drug effects
  • Cadherins / genetics
  • Cadherins / metabolism
  • Cell Death / drug effects
  • Cerebral Cortex / pathology
  • Docosahexaenoic Acids / pharmacology*
  • Endoplasmic Reticulum Stress / drug effects
  • Mice, Inbred C57BL
  • Mice, Transgenic
  • Neurons / drug effects
  • Neurons / metabolism
  • Neurons / pathology*
  • Protein Multimerization*

Substances

  • Amyloid beta-Peptides
  • Cadherins
  • fat1 protein, mouse
  • Docosahexaenoic Acids