Soybean-Derived Phytoalexins Improve Cognitive Function through Activation of Nrf2/HO-1 Signaling Pathway

Int J Mol Sci. 2018 Jan 16;19(1):268. doi: 10.3390/ijms19010268.

Abstract

As soy-derived glyceollins are known to induce antioxidant enzymes in various types of cells and tissues, we hypothesized that the compounds could protect neurons from damage due to reactive oxygen species (ROS). In order to examine the neuroprotective effect of glyceollins, primary cortical neurons collected from mice and mouse hippocampal HT22 cells were challenged with glutamate. Glyceollins attenuated glutamate-induced cytotoxicity in primary cortical neuron isolated from mice carrying wild-type nuclear factor (erythroid-derived 2)-like 2 (Nrf2), but the compounds were ineffective in those isolated from Nrf2 knockout mice, suggesting the involvement of the Nrf2 signaling pathway in glyceollin-mediated neuroprotection. Furthermore, the inhibition of heme oxygenase-1 (HO-1), a major downstream enzyme of Nrf2, abolished the suppressive effect of glyceollins against glutamate-induced ROS production and cytotoxicity, confirming that activation of HO-1 by glyceollins is responsible for the neuroprotection. To examine whether glyceollins also improve cognitive ability, mice pretreated with glyceollins were challenged with scopolamine and subjected to behavioral tests. Glyceollins attenuated scopolamine-induced cognitive impairment of mice, but failed to enhance memory in Nrf2 knockout mice, suggesting that the memory-enhancing effect is also mediated by the Nrf2 signaling pathway. Overall, glyceollins showed neuroprotection against glutamate-induced damage, and attenuated scopolamine-induced memory deficits in an Nrf2-dependent manner.

Keywords: HO-1; MAPK; Nrf2; glyceollins; neuroprotection; phytoalexins; soybean.

MeSH terms

  • Acetylcholinesterase / metabolism
  • Amnesia / pathology
  • Amnesia / physiopathology
  • Animals
  • Antioxidant Response Elements / genetics
  • Cell Death / drug effects
  • Cell Nucleus / drug effects
  • Cell Nucleus / metabolism
  • Cell Separation
  • Cells, Cultured
  • Cerebral Cortex / pathology
  • Cognition / drug effects*
  • Disease Models, Animal
  • Glutamic Acid / toxicity
  • Glycine max / chemistry*
  • Heme Oxygenase-1 / metabolism*
  • Humans
  • Male
  • Mice, Inbred C57BL
  • Mice, Knockout
  • NF-E2-Related Factor 2 / metabolism*
  • Neurons / drug effects
  • Neurons / pathology
  • Phytoalexins
  • Protein Kinase Inhibitors / pharmacology
  • Protein Transport / drug effects
  • Pterocarpans / pharmacology
  • Reactive Oxygen Species / metabolism
  • Scopolamine
  • Sesquiterpenes / pharmacology*
  • Signal Transduction / drug effects*
  • Transcriptional Activation / drug effects

Substances

  • NF-E2-Related Factor 2
  • Protein Kinase Inhibitors
  • Pterocarpans
  • Reactive Oxygen Species
  • Sesquiterpenes
  • Glutamic Acid
  • glyceollin
  • Scopolamine
  • Heme Oxygenase-1
  • Acetylcholinesterase
  • Phytoalexins