| Literature DB >> 26876114 |
Patrick Lo1, Christian Crouzet2, Vitaly Vasilevko3, Bernard Choi4.
Abstract
Cerebral amyloid angiopathy (CAA) is a neurovascular disease that is strongly associated with an increase in the number and size of spontaneous microbleeds. Conventional methods of magnetic resonance imaging for detection of microbleeds, and positron emission tomography with Pittsburgh Compound B imaging for amyloid deposits, can separately demonstrate the presence of microbleeds and CAA in affected brains in vivo; however, there still is a critical need for strong evidence that shows involvement of CAA in microbleed formation. Here, we show in a Tg2576 mouse model of Alzheimer's disease, that the combination of histochemical staining and an optical clearing method called optical histology, enables simultaneous, co-registered three-dimensional visualization of cerebral microvasculature, microbleeds, and amyloid deposits. Our data suggest that microbleeds are localized within the brain regions affected by vascular amyloid deposits. All observed microhemorrhages (n=39) were in close proximity (0 to 144 μm) with vessels affected by CAA. Our data suggest that the predominant type of CAA-related microbleed is associated with leaky or ruptured hemorrhagic microvasculature. The proposed methodological and instrumental approach will allow future study of the relationship between CAA and microbleeds during disease development and in response to treatment strategies.Entities:
Keywords: Amyloid-β; Cerebral amyloid angiopathy; DiI; Intracerebral hemorrhage; Microhemorrhages; Prussian blue; Stroke; Thioflavin S
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Year: 2016 PMID: 26876114 PMCID: PMC4814270 DOI: 10.1016/j.mvr.2016.02.002
Source DB: PubMed Journal: Microvasc Res ISSN: 0026-2862 Impact factor: 3.514