Pomegranate ellagitannin-gut microbial-derived metabolites, urolithins, inhibit neuroinflammation in vitro

Nutr Neurosci. 2019 Mar;22(3):185-195. doi: 10.1080/1028415X.2017.1360558. Epub 2017 Aug 7.

Abstract

Objectives: Urolithins, ellagitannin-gut microbial-derived metabolites, have been reported to mediate pomegranate's neuroprotective effects against Alzheimer's disease (AD), but there are limited data on their effects against neuroinflammation. Herein, we: (1) evaluated whether urolithins (urolithins A and B and their methylated derivatives) attenuate neuroinflammation in murine BV-2 microglia and human SH-SY5Y neurons, and (2) evaluated hippocampus of transgenic AD (R1.40) mice administered a pomegranate extract (PE; 100 or 200 mg/kg/day for 3 weeks) for inflammatory biomarkers.

Methods: Effects of urolithins (10 μM) on inflammatory biomarkers were evaluated in lipopolysaccharide (LPS)-stimulated BV-2 microglia. In a non-contact co-culture cell model, SH-SY5Y cell viability was assessed after exposure to media collected from LPS-BV-2 cells treated with or without urolithins. Effects of urolithins on apoptosis and caspase 3/7 and 9 release from H2O2-induced oxidative stress of BV-2 and SH-SY5Y cells were assessed. Hippocampal tissues of vehicle and PE-treated transgenic R1.40 mice were evaluated for gene expression of inflammatory biomarkers by qRT-PCR.

Results: Urolithins decreased media levels of nitric oxide, interleukin 6 (IL-6), prostaglandin E2, and tumor necrosis factor alpha from LPS-BV-2 microglia. In the co-culture cell model, media from LPS-BV-2 cells treated with urolithins preserved SH-SY5Y cell viability greater than media from cells treated without urolithins. Urolithins mitigated apoptosis and caspase 3/7 and 9 release from H2O2-induced oxidative stress of BV-2 and SH-SY5Y cells. While not statistically significant, inflammatory biomarkers (TNF-α, COX-2, IL-1, and IL-6) appeared to follow a decreasing trend in the hippocampus of high-dose PE-treated animals compared to controls.

Discussion: The attenuation of neuroinflammation by urolithins may contribute, in part, toward pomegranate's neuroprotective effects against AD.

Keywords: Gut microflora; Neuroinflammation; Neuroprotective; Pomegranate; Urolithins.

MeSH terms

  • Animals
  • Apoptosis / drug effects
  • Cell Line
  • Cell Line, Tumor
  • Coumarins / administration & dosage*
  • Encephalitis / chemically induced
  • Encephalitis / metabolism*
  • Encephalitis / prevention & control
  • Gastrointestinal Microbiome*
  • Hippocampus / drug effects
  • Hippocampus / metabolism
  • Humans
  • Hydrolyzable Tannins / metabolism*
  • Inflammation Mediators
  • Lipopolysaccharides / administration & dosage
  • Lythraceae / metabolism*
  • Mice, Transgenic
  • Microglia / drug effects
  • Microglia / metabolism
  • Neurons / drug effects
  • Neurons / metabolism
  • Neuroprotective Agents / administration & dosage*
  • Oxidative Stress / drug effects
  • Plant Extracts / administration & dosage

Substances

  • Coumarins
  • Hydrolyzable Tannins
  • Inflammation Mediators
  • Lipopolysaccharides
  • Neuroprotective Agents
  • Plant Extracts
  • ellagitannin
  • urolithin B
  • 3,8-dihydroxy-6H-dibenzo(b,d)pyran-6-one