| Literature DB >> 12177216 |
Thomas Mueggler1, Christine Sturchler-Pierrat, Diana Baumann, Martin Rausch, Matthias Staufenbiel, Markus Rudin.
Abstract
APP23 transgenic mice overexpressing amyloid precursor protein (APP751) reproduce neuropathological changes associated with Alzheimer's disease such as high levels of amyloid plaques, cerebral amyloid angiopathy, and associated vascular pathologies. Functional magnetic resonance imaging (fMRI) was applied to characterize brain functionality in these mice through global pharmacological stimulation. The cerebral hemodynamic response to infusion of the GABA(A) antagonist bicuculline was significantly reduced in aged APP23 mice compared with age-matched wild-type littermates. This is in part attributable to a compromised cerebrovascular reactivity, as revealed by the reduced responsiveness to vasodilatory stimulation by acetazolamide. The study shows that fMRI is a sensitive tool to phenotype genetically engineered animals modeling neuropathologies.Entities:
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Year: 2002 PMID: 12177216 PMCID: PMC6757895 DOI: 20026680
Source DB: PubMed Journal: J Neurosci ISSN: 0270-6474 Impact factor: 6.167