6-Shogaol has anti-amyloidogenic activity and ameliorates Alzheimer's disease via CysLT1R-mediated inhibition of cathepsin B

Biochem Biophys Res Commun. 2016 Aug 12;477(1):96-102. doi: 10.1016/j.bbrc.2016.06.026. Epub 2016 Jun 7.

Abstract

Although 6-shogaol, a constituent of ginger, has been reported to have anti-inflammatory and anti-oxidant effects on neuronal cells, the effects of 6-shogaol on Alzheimer's disease (AD) have not yet been investigated. Here we aimed to determine whether 6-shogaol exerts neuroprotective effects against AD. Specifically, we investigated the effects of 6-shogaol on the cysteinyl leukotriene 1 receptor (CysLT1R), a major factor in AD pathogenesis. Moreover, we clarified the relationship between CysLT1R and cathepsin B, a cysteine protease. We used in vitro and in vivo models to determine whether 6-shogaol inhibits CysLT1R/cathepsin B in an amyloid-beta (Aβ; 1-42)-induced model of neurotoxicity. We first confirmed that CysLT1R and cathepsin B are upregulated by Aβ (1-42) and that CysLT1R activation induces cathepsin B. In contrast, we found that 6-shogaol-mediated inhibition of CysLT1R downregulates cathepsin B in both in vitro and in vivo models. Furthermore, we found that 6-shogaol-mediated inhibition of CysLT1R/cathepsin B reduces Aβ deposition in the brain and ameliorates behavioral deficits in APPSw/PS1-dE9 Tg mice. Our results indicate that 6-shogaol is a CysLT1R/cathepsin B inhibitor and is a novel potential therapeutic agent for the treatment of various neurodegenerative diseases, including AD.

Keywords: 6-Shogaol; Alzheimer’s disease; Cathepsin B; Cysteinyl leukotriene 1 receptor; Ginger.

MeSH terms

  • Alzheimer Disease / prevention & control*
  • Amyloid beta-Peptides / antagonists & inhibitors*
  • Animals
  • Avoidance Learning / drug effects
  • Brain / drug effects
  • Brain / enzymology
  • Brain / metabolism
  • Catechols / pharmacology*
  • Cathepsin B / antagonists & inhibitors*
  • Cell Line
  • Male
  • Maze Learning / drug effects
  • Mice
  • Mice, Inbred C57BL
  • Mice, Transgenic
  • Peptide Fragments / antagonists & inhibitors*
  • Receptors, Leukotriene / physiology*

Substances

  • Amyloid beta-Peptides
  • Catechols
  • Peptide Fragments
  • Receptors, Leukotriene
  • amyloid beta-protein (1-42)
  • shogaol
  • Cathepsin B
  • leukotriene D4 receptor