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Reductions in levels of the Alzheimer’s amyloid peptide after oral administration of ginsenosides

Bibliographic

Year of Publication:
2006
Contact PI Name:
Christopher B. Eckman
Contact PI Affiliation:
Mayo Clinic College of Medicine, Departments of Pharmacology and Neuroscience, Jacksonville, Florida, USA
Co-Authors:
Feng Chen, Elizabeth A. Eckman
Primary Reference (PubMED ID):
Funding Source:
Not Reported
Study Goal and Principal Findings:

The study goal is to investigate effects of ginsenosides on Aβ levels. Ginsenosides, such asRe, Rg1, Rg3, Rb1, Rb2, panaxadiol, panaxatriol, pseudoginsenoside F11, and notoginsenoside R1, are a Chinese remedy commonly used in China to treat Alzheimer's disease-like symptoms. Ginseng has low toxicity when taken orally. In this study, they measured Aβ levels in cell and animal models. Results showed in the cell-based model system that ginseng reduced levels of Aβ in the conditioned medium. Other ginsenosides also reduced Aβ concentrations in a dose-dependent manner, especially Rg3 with an IC50 under 25 µM. In Tg2576 mice, the ginsenosides reduced brain Aβ levels after a single dose. These results imply that ginsenosides could be beneficial for AD patients.

Therapeutic Agent

Therapeutic Information:
Therapy Type:
Natural Product
Therapeutic Agent:
Gensenosides
Therapeutic Target:
Multi Target

Animal Model

Model Information:
Species:
Mouse
Model Type:
APP
Strain/Genetic Background:
Not Reported

Experimental Design

Is the following information reported in the study?:
Power/Sample Size Calculation
Randomized into Groups
Blinded for Treatment
Blinded for Outcome Measures
Pharmacokinetic Measures
Pharmacodynamic Measures
Toxicology Measures
ADME Measures
Biomarkers
Dose
Formulation
Route of Delivery
Duration of Treatment
Frequency of Administration
Age of Animal at the Beginning of Treatment
Age of Animal at the End of Treatment
Sex as a Biological Variable
Study Balanced for Sex as a Biological Variable
Number of Premature Deaths
Number of Excluded Animals
Statistical Plan
Genetic Background
Inclusion/Exclusion Criteria Included
Conflict of Interest

Outcomes

Outcome Measured
Outcome Parameters
Biochemical
Intracellular beta Amyloid Peptide
Brain-beta Amyloid Peptide 40
Brain-beta Amyloid Peptide 42
Cell Biology
Cell Viability
Pharmacodynamics
Target Engagement (Reduction beta Amyloid Peptides-Brain)