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Acteoside of Callicarpa dichotoma attenuates scopolamine-induced memory impairments.

Abstract
We previously reported that ten phenylethanoid glycosides including acteoside isolated from the leaves and twigs of Callicarpa dichotoma significantly attenuated glutamate-induced neurotoxicity. In the present study, we examined anti-amnesic activity of acteoside using scopolamine-induced (1 mg/kg body weight, s.c.) amnesic mice with both passive avoidance and Morris water maze tests. Acute oral treatment (single administration prior to scopolamine treatment) of mice with acteoside (1.0, 2.5 mg/kg body weight) significantly mitigated scopolamine-induced memory deficits in the passive avoidance test. It is interesting to note that prolonged oral daily treatment of mice with much lower amount (0.1 mg/kg body weight) of acteoside for 10 d reversed the scopolamine-induced memory deficits. In the Morris water maze, prolonged oral treatment with acteoside (prolonged daily administration of 1.0 mg/kg body weight for 10 d) significantly ameliorated scopolamine-induced memory deficits showing the formation of long-term and/or short-term spatial memory. We suggest, therefore, that acteoside has anti-amnesic activity that may ultimately hold significant therapeutic value in alleviating certain memory impairment observed in Alzheimer's disease.
AuthorsKi Yong Lee, Eun Ju Jeong, Heum-Sook Lee, Young Choong Kim
JournalBiological & pharmaceutical bulletin (Biol Pharm Bull) Vol. 29 Issue 1 Pg. 71-4 (Jan 2006) ISSN: 0918-6158 [Print] Japan
PMID16394513 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Glucosides
  • Muscarinic Antagonists
  • Phenols
  • acteoside
  • Scopolamine
Topics
  • Animals
  • Avoidance Learning (drug effects)
  • Callicarpa (chemistry)
  • Cognition (drug effects)
  • Glucosides (pharmacology)
  • Male
  • Maze Learning (drug effects)
  • Memory Disorders (chemically induced, prevention & control)
  • Mice
  • Mice, Inbred ICR
  • Muscarinic Antagonists (toxicity)
  • Phenols (pharmacology)
  • Scopolamine (antagonists & inhibitors, toxicity)

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