Ameliorating the effect of astragaloside IV on learning and memory deficit after chronic cerebral hypoperfusion in rats

Molecules. 2015 Jan 23;20(2):1904-21. doi: 10.3390/molecules20021904.

Abstract

Astragaloside IV (AS-IV) has been reported to have a prominent antioxidant effect and was proposed as a promising agent for the prevention of neurodegenerative disorders accompanied by cognitive impairment. The present study investigated the ameliorating effect of AS-IV on learning and memory deficits induced by chronic cerebral hypoperfusion in rats. Rats were treated with two doses of AS-IV (10 and 20 mg/kg, i.p.) daily for 28 days starting from the 5th week after permanent bilateral common carotid artery occlusion. AS-IV treatment (at dose of 20 mg/kg) significantly improved the spatial learning and memory deficits assessed using the Morris water maze test in rats with chronic cerebral hypoperfusion. AS-IV significantly attenuated neuronal apoptosis as well as the levels of superoxide dismutase and lipid peroxidation markers, including malondialdehyde and 4-hydroxy-2-nonenal, in the hippocampus. AS-IV also significantly reduced 8-hydroxy-2'-deoxyguanosine expression, a maker of oxidative DNA damage, while significantly inhibited the astrocyte and microglia activation in the hippocampus. The results indicate that AS-IV has therapeutic potential for the prevention of dementia caused by cerebral hypoperfusion and suggest that the ameliorating effect of AS-IV on learning and memory deficits might be the result of suppressing neuronal apoptosis and oxidative damage in the hippocampus.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antioxidants / pharmacology
  • Antioxidants / therapeutic use*
  • Apoptosis
  • Calcium-Binding Proteins / metabolism
  • Carotid Artery Diseases / complications
  • Carotid Artery Diseases / drug therapy*
  • Cerebrovascular Circulation
  • Chronic Disease
  • Drug Evaluation, Preclinical
  • Glial Fibrillary Acidic Protein / metabolism
  • Hippocampus / blood supply
  • Hippocampus / drug effects
  • Hippocampus / pathology
  • Male
  • Maze Learning
  • Microfilament Proteins / metabolism
  • Neuroglia / physiology
  • Neuroprotective Agents / pharmacology
  • Neuroprotective Agents / therapeutic use*
  • Oxidative Stress
  • Rats, Sprague-Dawley
  • Saponins / pharmacology
  • Saponins / therapeutic use*
  • Triterpenes / pharmacology
  • Triterpenes / therapeutic use*

Substances

  • Aif1 protein, rat
  • Antioxidants
  • Calcium-Binding Proteins
  • Glial Fibrillary Acidic Protein
  • Microfilament Proteins
  • Neuroprotective Agents
  • Saponins
  • Triterpenes
  • astragaloside A