The flavonoid agathisflavone modulates the microglial neuroinflammatory response and enhances remyelination

Pharmacol Res. 2020 Sep:159:104997. doi: 10.1016/j.phrs.2020.104997. Epub 2020 Jun 11.

Abstract

Myelin loss is the hallmark of the demyelinating disease multiple sclerosis (MS) and plays a significant role in multiple neurodegenerative diseases. A common factor in all neuropathologies is the central role of microglia, the intrinsic immune cells of the central nervous system (CNS). Microglia are activated in pathology and can have both pro- and anti-inflammatory functions. Here, we examined the effects of the flavonoid agathisflavone on microglia and remyelination in the cerebellar slice model following lysolecithin induced demyelination. Notably, agathisflavone enhances remyelination and alters microglial activation state, as determined by their morphology and cytokine profile. Furthermore, these effects of agathisflavone on remyelination and microglial activation were inhibited by blockade of estrogen receptor α. Thus, our results identify agathisflavone as a novel compound that may act via ER to regulate microglial activation and enhance remyelination and repair.

Keywords: Agathisflavone; Estrogen receptors; Flavonoids; Microglia; Neuroinflammation; Remyelination.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Anti-Inflammatory Agents / pharmacology*
  • Biflavonoids / pharmacology*
  • Cell Differentiation / drug effects
  • Cell Proliferation / drug effects
  • Cerebellum / drug effects*
  • Cerebellum / immunology
  • Cerebellum / metabolism
  • Cerebellum / pathology
  • Cytokines / metabolism
  • Estrogen Receptor alpha / drug effects
  • Estrogen Receptor alpha / metabolism
  • Female
  • Green Fluorescent Proteins / genetics
  • Green Fluorescent Proteins / metabolism
  • Lysophosphatidylcholines / toxicity
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Transgenic
  • Microglia / drug effects*
  • Microglia / immunology
  • Microglia / metabolism
  • Microglia / pathology
  • Myelin Sheath / metabolism*
  • Neuroimmunomodulation / drug effects*
  • Oligodendroglia / drug effects*
  • Oligodendroglia / immunology
  • Oligodendroglia / metabolism
  • Oligodendroglia / pathology
  • Phenotype
  • Remyelination / drug effects*
  • Tissue Culture Techniques

Substances

  • Anti-Inflammatory Agents
  • Biflavonoids
  • Cytokines
  • Esr1 protein, mouse
  • Estrogen Receptor alpha
  • Lysophosphatidylcholines
  • enhanced green fluorescent protein
  • Green Fluorescent Proteins
  • agathisflavone