Fucoxanthinol from the Diatom Nitzschia Laevis Ameliorates Neuroinflammatory Responses in Lipopolysaccharide-Stimulated BV-2 Microglia

Mar Drugs. 2020 Feb 17;18(2):116. doi: 10.3390/md18020116.

Abstract

In recent years, microalgae have drawn increasing attention as a valuable source of functional food ingredients. Intriguingly, Nitzschia laevis is rich in fucoxanthinol that is seldom found in natural sources. Fucoxanthinol, a marine xanthophyll carotenoid, possesses various beneficial bioactivities. Nevertheless, it's not clear whether fucoxanthinol could exert anti-neuroinflammatory function. In light of these premises, the aim of the present study was to investigate the anti-inflammatory role of fucoxanthinol purified from Nitzschia laevis in Lipopolysaccharide (LPS)-stimulated microglia. The results showed that pre-treatment of fucoxanthinol remarkably attenuated the expression of LPS-induced nitric oxide synthase (iNOS) and cyclooxygenase-2 (COX-2), and the production of tumor necrosis factor-alpha (TNF-α), interleukin-6 (IL-6), prostaglandin E2 (PGE-2), nitric oxide (NO) and reactive oxygen species (ROS) induction. Modulation mechanism studies revealed that fucoxanthinol hampered nuclear factor-kappa B (NF-κB), Akt, and mitogen-activated protein kinase (MAPK) pathways. Meanwhile, fucoxanthinol led to the enhancement of nuclear translocation of NF-E2-related factor 2 (Nrf2), and the upregulation of heme oxygenase-1 (HO-1) and NAD(P)H: quinone oxidoreductase 1 (NQO-1). Taken together, the results indicated that fucoxanthinol obtained from Nitzschia laevis had great potential as a neuroprotective agent in neuroinflammation and neurodegenerative disorders.

Keywords: Akt; MAPKs; NF-κB; Nitzschia laevis; Nrf2; anti-inflammation; fucoxanthinol.

MeSH terms

  • Animals
  • Anti-Inflammatory Agents / pharmacology
  • Cell Line
  • Cell Survival / drug effects
  • Cyclooxygenase 2 / metabolism
  • Diatoms*
  • Dinoprostone / metabolism
  • Heme Oxygenase-1 / metabolism
  • Inflammation / chemically induced
  • Inflammation / drug therapy*
  • Interleukin-6 / metabolism
  • Lipopolysaccharides
  • Membrane Proteins / metabolism
  • Mice
  • Microglia / drug effects*
  • Microglia / metabolism*
  • NAD(P)H Dehydrogenase (Quinone) / metabolism
  • NADPH Oxidases / metabolism
  • Nitric Oxide / metabolism
  • Nitric Oxide Synthase Type II / metabolism
  • Tumor Necrosis Factor-alpha / metabolism
  • beta Carotene / analogs & derivatives*
  • beta Carotene / chemistry
  • beta Carotene / pharmacology

Substances

  • Anti-Inflammatory Agents
  • Interleukin-6
  • Lipopolysaccharides
  • Membrane Proteins
  • Tumor Necrosis Factor-alpha
  • interleukin-6, mouse
  • beta Carotene
  • Nitric Oxide
  • fucoxanthinol
  • Nitric Oxide Synthase Type II
  • Nos2 protein, mouse
  • Heme Oxygenase-1
  • Hmox1 protein, mouse
  • Cyclooxygenase 2
  • NADPH Oxidases
  • NAD(P)H Dehydrogenase (Quinone)
  • Nqo1 protein, mouse
  • Dinoprostone