Tectochrysin from Alpinia Oxyphylla Miq. alleviates Aβ1-42 induced learning and memory impairments in mice

Eur J Pharmacol. 2019 Jan 5:842:365-372. doi: 10.1016/j.ejphar.2018.11.002. Epub 2018 Nov 6.

Abstract

Alzheimer's disease (AD), a neurodegenerative disease, is diagnosed by impaired learning and memory in elderly individuals. Tectochrysin (TEC) is a flavonoid compound isolated from Alpinia Oxyphylla Miq., which has been traditionally used for the treatment of diarrhea, salivation, diuresis and dementia. In our study, model mice with AD induced by intracerebroventricular injection of Aβ1-42 were used to determine the role of TEC on memory retrieval. The results revealed that AD mice received intracerebroventricular injection of TEC (140 µg/kg) showed improved spatial memory performance and down-regulated expressions of β-secretase and accumulation of Aβ1-42 in brain tissues. TEC also decreased the concentration of malondialdehyde and total cholinesterase, and increased activities of both antioxidant superoxide dismutase and glutathione peroxidase in hippocampal and cortex. In addition, Aβ1-42 induced injury of neurons in hippocampal CA1 layer was rehabilitated in TEC treated mice. These findings highlight the beneficial role of TEC in amnestic mice induced by Aβ1-42 through the down-regulation of Aβ1-42 accumulation, oxidative stress, and total cholinesterase. Our study indicated a therapeutic potential of TEC in the treatment of AD.

Keywords: Alzheimer's disease; Behavioral tests; Neuroprotective effect; Tectochrysin.

MeSH terms

  • Alpinia / chemistry*
  • Amyloid Precursor Protein Secretases / metabolism
  • Amyloid beta-Peptides / metabolism
  • Amyloid beta-Peptides / toxicity*
  • Animals
  • Avoidance Learning / drug effects
  • CA1 Region, Hippocampal / cytology
  • CA1 Region, Hippocampal / drug effects
  • CA1 Region, Hippocampal / metabolism
  • CA1 Region, Hippocampal / physiology
  • Cerebral Cortex / cytology
  • Cerebral Cortex / drug effects
  • Cerebral Cortex / metabolism
  • Cerebral Cortex / physiology
  • Cholinesterases / metabolism
  • Dose-Response Relationship, Drug
  • Flavonoids / pharmacology*
  • Locomotion / drug effects
  • Locomotion / physiology
  • Maze Learning / drug effects
  • Memory / drug effects*
  • Mice
  • Neurons / drug effects
  • Peptide Fragments / metabolism
  • Peptide Fragments / toxicity*
  • Spatial Memory / drug effects

Substances

  • Amyloid beta-Peptides
  • Flavonoids
  • Peptide Fragments
  • amyloid beta-protein (1-42)
  • tectochrysin
  • Cholinesterases
  • Amyloid Precursor Protein Secretases