Please use this identifier to cite or link to this item:
|Title:||Comparison of vascular perturbations in an Aβ-injected animal model and in AD brain|
Jae K. Ryu
Patrick L. McGeer
James G. McLarnon
The University of British Columbia
|Keywords:||Biochemistry, Genetics and Molecular Biology;Medicine;Neuroscience|
|Citation:||International Journal of Alzheimer's Disease. (2011)|
|Abstract:||The validity of amyloid-β peptide (A1-42) intrahippocampal injection, as an animal model of Alzheimer's disease (AD), has previously been considered in terms of inflammatory reactivity and neuronal damage. In this work, we have extended the testing of the animal model to vasculature by comparison of selected properties of microvessels in vivo with those in human AD brain tissue. The injection of Aβ 1-42 , relative to control PBS (phosphate buffered saline), increased the mean number of microvessels and diminished the mean length of microvessels in the molecular layer of dentate gyrus. The animal model showed Aβ 1-42 , but not PBS, injection was associated with abnormalities in morphology of microvessels which were characterized as looping, fragmented, knob-like, uneven, and constricted. In particular, numbers of constricted microvessels, defined as vessels with diameters less than 3m, were considerably enhanced for Aβ 1-42 , compared to PBS, injection. In comparison, human AD brain demonstrated an elevated number of microvessels with a diminished mean length relative to nondemented (ND) brain. Additionally, microvessel perturbations in AD brain showed a similar pattern of morphological abnormalities to those observed in A1-42-injected rat hippocampus. Constricted microvessels were a prominent feature of AD brain but were rarely observed in ND tissue. These results provide the first evidence that a peptide-injection animal model exhibits a commonality in perturbations of microvessels compared with those evident in AD brain. © 2011 Nattinee Jantaratnotai et al.|
|Appears in Collections:||Scopus 2011-2015|
Files in This Item:
There are no files associated with this item.
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.