Schisantherin A recovers Aβ-induced neurodegeneration with cognitive decline in mice

Physiol Behav. 2014 Jun 10:132:10-6. doi: 10.1016/j.physbeh.2014.04.046. Epub 2014 May 8.

Abstract

Schisantherin A (STA) is a main bioactive lignan isolated from Schisandra chinensis (Turcz.) Baill., which has been widely used as a tonic in traditional Chinese medicine for many years. Lots of studies have reported that STA exhibited anti-inflammatory and antioxidant effects. This paper was designed to investigate the effects of STA on cognitive function and neurodegeneration in the mouse control of Alzheimer's disease (AD) induced by Aβ1-42. It was found that successive intracerebroventricular (ICV) administration of STA (0.01 and 0.1mg/kg) for 5days significantly attenuated Aβ1-42-induced learning and memory impairment as measured by the Y-maze test, shuttle-box test and Morris water maze test. Furthermore, STA at a dose of 0.1mg/kg restored the activities of superoxide dismutase (SOD) and glutathione peroxidase (GSH-Px) as well as the levels of Aβ1-42, malondialdehyde (MDA) and glutathione (GSH) to some extent in the hippocampus and cerebral cortex. It also noticeably improved the histopathological changes in the hippocampus. The results suggested that STA might protect against cognitive deficits, oxidative stress and neurodegeneration induced by Aβ1-42, and serve as a potential agent in treatment of AD.

Keywords: Alzheimer's disease; Aβ(1–42); Cognition enhancing activity; Histopathological changes; Schisantherin A; Successive intracerebroventricular.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amyloid beta-Peptides / toxicity
  • Analysis of Variance
  • Animals
  • Antioxidants / chemistry
  • Antioxidants / therapeutic use*
  • Brain / drug effects
  • Brain / metabolism
  • Cognition Disorders / chemically induced
  • Cognition Disorders / complications
  • Cognition Disorders / drug therapy*
  • Cognition Disorders / pathology
  • Cyclooctanes / chemistry
  • Cyclooctanes / therapeutic use*
  • Dioxoles / chemistry
  • Dioxoles / therapeutic use*
  • Disease Models, Animal
  • Glutathione / metabolism
  • Glutathione Peroxidase / metabolism
  • Injections, Intraventricular
  • Lignans / chemistry
  • Lignans / therapeutic use*
  • Male
  • Malondialdehyde / metabolism
  • Maze Learning / drug effects
  • Mice
  • Mice, Inbred Strains
  • Neurodegenerative Diseases / chemically induced
  • Neurodegenerative Diseases / complications
  • Neurodegenerative Diseases / drug therapy*
  • Neurodegenerative Diseases / pathology
  • Peptide Fragments / toxicity
  • Superoxide Dismutase / metabolism

Substances

  • Amyloid beta-Peptides
  • Antioxidants
  • Cyclooctanes
  • Dioxoles
  • Lignans
  • Peptide Fragments
  • amyloid beta-protein (1-42)
  • Malondialdehyde
  • schizandrer A
  • Glutathione Peroxidase
  • Superoxide Dismutase
  • Glutathione