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Bacopa monniera extract reduces amyloid levels in PSAPP mice

Bibliographic

Year of Publication:
2006
Contact PI Name:
Bala V. Manyam
Contact PI Affiliation:
Department of Neurology, Texas A&M University System HSC College of Medicine, Temple, Texas, USA
Co-Authors:
Leigh A. Holcomb, Muralikrishnan Dhanasekaran, Angie R. Hitt, Keith A. Young, Mark Riggs
Primary Reference (PubMED ID):
Funding Source:
Scott Sherwood and Brindley Foundation
Helen Vosburg, McCrillus Plummer and Robert Edward Lee Plummer Jr. Endowed Fund
United States Department of Veterans Affairs (VA)
Study Goal and Principal Findings:

PSAPP mice expressing the “Swedish” amyloid precursor protein and M146L presenilin-1 mutations are a well characterized model for spontaneous amyloid plaque formation. Bacopa monniera has a long history of use in India as an anti-aging and memory-enhancing ethnobotanical therapy. To evaluate the effect of Bacopa monniera extract (BME) on amyloid (Aβ) pathology in PSAPP mice, two doses of BME (40 or 160 mg/kg/day) were administered starting at 2 months of age for either 2 or 8 months. The present data suggests that BME lowers Aβ 1-40 and 1-42 levels in cortex by as much as 60%, and reverses Y-maze performance and open field hyperlocomotion behavioral changes present in PSAPP mice. The areas encompassed by Congo Red-positive fibrillar amyloid deposits, however, were not altered by BME treatment. The data suggest that BME has potential application in Alzheimer’s disease therapeutics.

Therapeutic Agent

Therapeutic Information:
Therapy Type:
Natural Product
Therapeutic Agent:
Bacopa Monniera Extract (BME)
Therapeutic Target:
Multi Target

Animal Model

Model Information:
Species:
Mouse
Model Type:
APPxPS1
Strain/Genetic Background:
B6SJL

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
Behavioral
Y Maze
Open Field Test
Histopathology
beta Amyloid Load
Dense-core/Compact Plaques
Biochemical
Brain-beta Amyloid Peptide 40
Brain-beta Amyloid Peptide 42
Pharmacodynamics
Target Engagement (Reduction beta Amyloid Peptides-Brain)
Toxicology
Body Weight