Eclalbasaponin II Ameliorates the Cognitive Impairment Induced by Cholinergic Blockade in Mice

Neurochem Res. 2018 Feb;43(2):351-362. doi: 10.1007/s11064-017-2430-6. Epub 2017 Nov 21.

Abstract

Eclalbasaponin II derived from Eclipta prostrata L. (Asteraceae) has been reported to have anti-fibrotic, anti-bacterial and autophagic activities, but its effect on cognitive function has not been investigated. We studied the effect of eclalbasaponin II on cholinergic blockade-induced memory impairment in mice using the passive avoidance, Y-maze, and Morris water maze tasks. Eclalbasaponin II (10 or 20 mg/kg, p.o.) significantly ameliorated the cognitive dysfunction induced by scopolamine in the passive avoidance, Y-maze, and the Morris water maze tasks. To identify the mechanism of the memory-ameliorating effect of eclalbasaponin II, acetylcholinesterase (AChE) activity assay, Western blot analysis and electrophysiology were conducted. Eclalbasaponin II inhibited the AChE activity in ex vivo study, and the administration of eclalbasaponin II and its metabolite, echinocystic acid, increased the phosphorylation levels of memory-related signaling molecules, including protein kinase B (Akt) and glycogen synthase kinase-3β (GSK-3β), in the hippocampus. Although eclalbasaponin II did not affect hippocampal long term potentiation (LTP), echinocystic acid significantly enhanced hippocampal LTP formation (30 μM). These results suggest that eclalbasaponin II ameliorates cholinergic blockade-induced cognitive impairment via AChE inhibition, LTP formation and the activation of Akt-GSK-3β signaling, and that eclalbasaponin II may be a useful to treat cognitive impairment derived from cholinergic dysfunction.

Keywords: Eclalbasaponin II; Glycogen synthase kinase 3β; Learning and memory; Long-term potentiation; Protein kinase B.

MeSH terms

  • Animals
  • Avoidance Learning / drug effects
  • Cholinergic Antagonists / pharmacology*
  • Cholinesterase Inhibitors / pharmacology*
  • Cognition / drug effects
  • Cognitive Dysfunction / drug therapy
  • Cognitive Dysfunction / metabolism*
  • Disease Models, Animal
  • Glycogen Synthase Kinase 3 beta / metabolism
  • Hippocampus / drug effects
  • Hippocampus / metabolism
  • Long-Term Potentiation / drug effects
  • Male
  • Memory / drug effects
  • Memory Disorders / chemically induced
  • Mice
  • Saponins / metabolism*
  • Scopolamine / pharmacology*

Substances

  • Cholinergic Antagonists
  • Cholinesterase Inhibitors
  • Saponins
  • eclalbasaponin II
  • Scopolamine
  • Glycogen Synthase Kinase 3 beta