Suppression of Lipopolysaccharide-Induced Neuroinflammation by Morin via MAPK, PI3K/Akt, and PKA/HO-1 Signaling Pathway Modulation

J Agric Food Chem. 2017 Jan 18;65(2):373-382. doi: 10.1021/acs.jafc.6b05147. Epub 2017 Jan 9.

Abstract

Morin is a flavonoid isolated from certain fruits and Chinese herbs and is known to possess various medicinal properties. In this study, we investigated the anti-inflammatory effects of morin on lipopolysaccharide (LPS)-induced microglial activation, both in vitro and in vivo. We found that morin inhibited inducible nitric oxide synthase (iNOS) and pro-inflammatory cytokines in LPS-stimulated BV2 microglial cells. Furthermore, morin suppressed the microglial activation and cytokine expression in the brains of LPS-stimulated mice. Subsequent mechanistic studies revealed that morin inhibited the action of LPS-activated mitogen-activated protein kinases (MAPKs), protein kinase B (Akt) phosphorylation, nuclear factor-κB (NF-κB), and activating protein-1 (AP-1). Further, the phosphorylation and DNA binding activity of cAMP responsive element binding protein (CREB) was enhanced by morin. Moreover, morin suppressed the LPS-induced expression of nicotinamide adenine dinucleotide phosphate (NADPH) oxidase subunits, while it increased heme oxygenase-1 (HO-1) expression and nuclear factor erythroid 2-related factor 2 (Nrf2) activation. Therefore, our data suggest that morin exerts anti-inflammatory effects in LPS-stimulated microglia by downregulating MAPK and phosphatidylinositol 3-kinase (PI3K)/Akt signaling pathways while upregulating protein kinase A (PKA)/CREB and Nrf2/HO-1 signaling pathways.

Keywords: anti-inflammation; microglia; molecular mechanisms; morin; neuroinflammation.

MeSH terms

  • Animals
  • Anti-Inflammatory Agents, Non-Steroidal / pharmacology*
  • Cyclic AMP-Dependent Protein Kinases / metabolism
  • Cytokines / metabolism
  • Flavonoids / pharmacology*
  • Heme Oxygenase-1 / metabolism
  • Inflammation / chemically induced
  • Inflammation / drug therapy*
  • Inflammation / metabolism*
  • Lipopolysaccharides / toxicity
  • Membrane Proteins / metabolism
  • Mice, Inbred ICR
  • Microglia / drug effects
  • Microglia / metabolism
  • Mitogen-Activated Protein Kinases / metabolism
  • Neuroprotective Agents / pharmacology
  • Phosphatidylinositol 3-Kinase
  • Proto-Oncogene Proteins c-akt / metabolism
  • Reactive Oxygen Species / metabolism
  • Sepsis / chemically induced
  • Sepsis / drug therapy
  • Signal Transduction / drug effects

Substances

  • Anti-Inflammatory Agents, Non-Steroidal
  • Cytokines
  • Flavonoids
  • Lipopolysaccharides
  • Membrane Proteins
  • Neuroprotective Agents
  • Reactive Oxygen Species
  • morin
  • Heme Oxygenase-1
  • Hmox1 protein, mouse
  • Phosphatidylinositol 3-Kinase
  • Proto-Oncogene Proteins c-akt
  • Cyclic AMP-Dependent Protein Kinases
  • Mitogen-Activated Protein Kinases