Fatty Acid-Derived N-acylethanolamines Dietary Supplementation Attenuates Neuroinflammation and Cognitive Impairment in LPS Murine Model

Nutrients. 2022 Sep 19;14(18):3879. doi: 10.3390/nu14183879.

Abstract

Neuroinflammation plays a critical role in the pathogenesis of most neurological and neurodegenerative diseases and therefore represents a potential therapeutic target. In this regard, accelerating the resolution process in chronic neuroinflammation may be an effective strategy to deal with the cognitive consequences of neuropathology and generalized inflammatory processes. N-acylethanolamine (NAE) derivatives of fatty acids, being highly active lipid mediators, possess pro-resolving activity in inflammatory processes and are promising agents for the suppression of neuroinflammation and its consequences. This paper is devoted to a study of the effects played by dietary supplement (DS), containing a composition of fatty acid-derived NAEs, obtained from squid Berryteuthis magister, on the hippocampal neuroinflammatory and memory processes. By detecting the production of pro-inflammatory cytokines and glial markers, a pronounced anti-inflammatory activity of DS was demonstrated both in vitro and in vivo. DS administration reversed the LPS-induced reduction in hippocampal neurogenesis and memory deterioration. LC-MS analysis revealed an increase in the production of a range of NAEs with well-documented anti-inflammatory activity in response to the administered lipid composition. To conclude, we found that tested DS suppresses the neuroinflammatory response by reducing glial activation, positively regulates neural progenitor proliferation, and attenuates hippocampal-dependent memory impairment.

Keywords: DHEA; EPEA; N-acylethanolamine; NAE; OEA; PEA; SEA; dietary supplement; fatty acid; hippocampus; memory; neurogenesis; neuroinflammation.

MeSH terms

  • Animals
  • Anti-Inflammatory Agents / pharmacology
  • Cognitive Dysfunction* / drug therapy
  • Cytokines / metabolism
  • Dietary Supplements
  • Disease Models, Animal
  • Ethanolamines
  • Fatty Acids / pharmacology
  • Hippocampus / metabolism
  • Lipopolysaccharides* / pharmacology
  • Mice
  • Neuroinflammatory Diseases

Substances

  • Anti-Inflammatory Agents
  • Cytokines
  • Ethanolamines
  • Fatty Acids
  • Lipopolysaccharides
  • N-acylethanolamines