Quantitative assessment of microvasculopathy in arcAβ mice with USPIO-enhanced gradient echo MRI
Author(s)
Klohs, JanDeistung, Andreas
Ielacqua, Giovanna D
Seuwen, Aline
Kindler, Diana
Schweser, Ferdinand
Vaas, Markus
Kipar, Anja
Reichenbach, Jürgen R
Rudin, Markus
Keywords
Institute of Pharmacology and ToxicologyInstitute of Veterinary Pathology
Institute of Biomedical Engineering
170 Ethics
610 Medicine & health
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https://dx.doi.org/10.5167/uzh-119398Abstract
Magnetic resonance imaging employing administration of iron oxide-based contrast agents is widely used to visualize cellular and molecular processes in vivo. In this study, we investigated the ability of [Formula: see text] and quantitative susceptibility mapping to quantitatively assess the accumulation of ultrasmall superparamagnetic iron oxide (USPIO) particles in the arcAβ mouse model of cerebral amyloidosis. Gradient-echo data of mouse brains were acquired at 9.4 T after injection of USPIO. Focal areas with increased magnetic susceptibility and [Formula: see text] values were discernible across several brain regions in 12-month-old arcAβ compared to 6-month-old arcAβ mice and to non-transgenic littermates, indicating accumulation of particles after USPIO injection. This was concomitant with higher [Formula: see text] and increased magnetic susceptibility differences relative to cerebrospinal fluid measured in USPIO-injected compared to non-USPIO-injected 12-month-old arcAβ mice. No differences in [Formula: see text] and magnetic susceptibility were detected in USPIO-injected compared to non-injected 12-month-old non-transgenic littermates. Histological analysis confirmed focal uptake of USPIO particles in perivascular macrophages adjacent to small caliber cerebral vessels with radii of 2-8 µm that showed no cerebral amyloid angiopathy. USPIO-enhanced [Formula: see text] and quantitative susceptibility mapping constitute quantitative tools to monitor such functional microvasculopathies.Date
2015-12-01Type
Journal ArticleIdentifier
oai:www.zora.uzh.ch:119398http://dx.doi.org/10.5167/uzh-119398
info:doi/10.1177/0271678X15621500
info:pmid/26661253