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An exploratory investigation of brain collateral circulation plasticity after cerebral ischemia in two experimental C57BL/6 mouse models

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Item Type:Article
Title:An exploratory investigation of brain collateral circulation plasticity after cerebral ischemia in two experimental C57BL/6 mouse models
Creators Name:Foddis, M. and Winek, K. and Bentele, K. and Mueller, S. and Blumenau, S. and Reichhart N, N. and Crespo-Garcia, S. and Harnett, D. and Ivanov, A. and Meisel, A. and Joussen, A. and Strauss, O. and Beule, D. and Dirnagl, U. and Sassi, C.
Abstract:Brain collateral circulation is an essential compensatory mechanism in response to acute brain ischemia. To study the temporal evolution of brain macro and microcollateral recruitment and their reciprocal interactions in response to different ischemic conditions, we applied a combination of complementary techniques (T2-weighted magnetic resonance imaging [MRI], time of flight [TOF] angiography [MRA], cerebral blood flow [CBF] imaging and histology) in two different mouse models. Hypoperfusion was either induced by permanent bilateral common carotid artery stenosis (BCCAS) or 60-min transient unilateral middle cerebral artery occlusion (MCAO). In both models, collateralization is a very dynamic phenomenon with a global effect affecting both hemispheres. Patency of ipsilateral posterior communicating artery (PcomA) represents the main variable survival mechanism and the main determinant of stroke lesion volume and recovery in MCAO, whereas the promptness of external carotid artery retrograde flow recruitment together with PcomA patency, critically influence survival, brain ischemic lesion volume and retinopathy in BCCAS mice. Finally, different ischemic gradients shape microcollateral density and size.
Keywords:Stroke, Collateral Vessels, Posterior Communicating Arterie, Middle Cerebral Artery Occlusion, Bilateral Common Carotid Artery Stenosis, Animals, Mice
Source:Journal of Cerebral Blood Flow and Metabolism
ISSN:0271-678X
Publisher:Sage Publications
Volume:40
Number:2
Page Range:276-287
Date:1 February 2020
Official Publication:https://doi.org/10.1177/0271678X19827251
PubMed:View item in PubMed

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