4.2 Article

Correlation Analysis of Capillary APOE, VEGF and eNOS Expression in Alzheimer Brains

Journal

CURRENT ALZHEIMER RESEARCH
Volume 8, Issue 2, Pages 197-202

Publisher

BENTHAM SCIENCE PUBL LTD
DOI: 10.2174/156720511795256026

Keywords

Alzheimer's disease; APOE; capillaries; blood-brain barrier; AD lesions

Ask authors/readers for more resources

Vasoactive regulatory and transport proteins can modify the transendothelial blood-brain barrier (BBB) transport of beta-amyloid. Dysfunction of one or more of these proteins is hypothesized to contribute to the pathogenesis of Alzheimer's disease (AD). In this study we investigated superior temporal and occipital cortical sections from ten AD and ten control group brains (CG). They were examined using immunohistochemical techniques staining for beta(42) amyloid, APOE, VEGF and eNOS. The densities of senile plaques (SPs) and APOE, VEGF and eNOS positive capillaries in each region and in each AD and CG condition were compared using nonparametric statistical analysis. In the AD cases, there were significant negative correlations between APOE positive capillaries and beta(42) amyloid SPs, and positive correlations between APOE positive capillaries and VEGF and eNOS positive capillaries. These results demonstrate the increased presence of APOE activity in AD brain capillaries, and that there is a positive correlation between the expression of APOE and each of VEGF and eNOS in the capillaries of AD brains. It is possible, therefore, that the down regulation of APOE in AD brains may contribute significantly to the pathogenesis of SP lesion development by modulating brain beta-amyloid burden. The specific interrelationship between APOE, VEGF and eNOS activity at the BBB requires further investigation.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.2
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available