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Imaging the Abeta-related neurotoxicity of Alzheimer disease.

Imaging the Abeta-related neurotoxicity of Alzheimer disease. Research Abstract Details 

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  • Imaging the Abeta-related neurotoxicity of Alzheimer disease. Abstract Text:

    herman morenoHerman Moreno,william e wuWilliam E Wu,thomas leeThomas Lee,adam brickmanAdam Brickman,richard mayeuxRichard Mayeux,truman r brownTruman R Brown,scott a smallScott A Small,herman morenoHerman Moreno,william e wuWilliam E Wu,thomas leeThomas Lee,adam brickmanAdam Brickman,richard mayeuxRichard Mayeux,truman r brownTruman R Brown,scott a smallScott A Small,

    BACKGROUND: Neurotoxicity related to the Abeta peptide is thought to be a primary mechanism of dysfunction in Alzheimer disease (AD). Although numerous imaging studies have observed brain dysfunction in AD, whether these imaged defects reflect Abeta-related neurotoxicity remains unknown. OBJECTIVE: To study Abeta-related neurotoxicity by means of functional imaging maps of the hippocampal formation in human patients and mouse models. DESIGN: Cross-sectional study comparing humans with AD and control subjects, cross-sectional study of J20 mice, a transgenic mouse model of AD, and a longitudinal study of flurbiprofen administration to transgenic mice. SETTING: Alzheimer disease research center. Subjects Eleven subjects with probable Alzheimer disease and 11 age-matched controls, plus J20 mice and wild-type littermates. INTERVENTIONS: In the first study, human subjects and controls underwent magnetic resonance imaging. In the second study, mice underwent imaging at 3, 6, 12, 15, and 21 months of age, for a total of 57 imaging experiments. In the third study, 12 J20 mice underwent imaging repeatedly over time; 6 received flurbiprofen to ameliorate Abeta-related neurotoxicity and 6 received vehicle control. MAIN OUTCOME MEASURES: Comparison of hippocampal functional maps. RESULTS: Among all hippocampal subregions, the entorhinal cortex was the dominant site of dysfunction observed in both human patients and J20 mice. Long-term administration of flurbiprofen rescued entorhinal cortex dysfunction in transgenic mice. CONCLUSION: Our results establish that the neurotoxicity related to the Abeta peptide can be captured in vivo by functional imaging and suggest hippocampal subregions most vulnerable to its toxic effects.

    Imaging the Abeta-related neurotoxicity of Alzheimer disease. Publishing Authors By Initials

    h morenoH Moreno,we wuWE Wu,t leeT Lee,a brickmanA Brickman,r mayeuxR Mayeux,tr brownTR Brown,sa smallSA Small,h morenoH Moreno,we wuWE Wu,t leeT Lee,a brickmanA Brickman,r mayeuxR Mayeux,tr brownTR Brown,sa smallSA Small,

    For similar nervous system diseases: neurotoxicity syndromes research abstracts see: nervous system diseases: neurotoxicity syndromes research

    PUBMED ID PMID:

    MEDLINE DATE:

    Imaging the Abeta-related neurotoxicity of Alzheimer disease. Journal Published:

    PUBLICATION TYPE: Research Support, Non-U.S. Gov

    Journal: Archives of neurology

    VOLUME: 64

    Page Numbers: 1467-77

    Journal Abbreviation: Arch. Neurol.

    ISSN: 0003-9942

    DAY: 20

    MONTH: Oct

    YEAR: 2007

    Imaging the Abeta-related neurotoxicity of Alzheimer disease. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 372436

    Imaging the Abeta-related neurotoxicity of Alzheimer disease. Keywords Mesh Terms:

    KEYWORDS: Neurotoxicity Syndromes

    MESH TERMS: pathology

    Chemical & Substance for Abstract: Imaging the Abeta-related neurotoxicity of Alzheimer disease. Information

    Substance Name: Flurbiprofen

    Registry Number: 5104-49-4

    Grant and Affiliation Information for Imaging the Abeta-related neurotoxicity of Alzheimer disease.

    AFFILIATION: Department of Neurology, Robert S. Furchgott Center for Neural and Behavioral Sciences, State University of New York, Downstate Medical Center, Brooklyn, NY, USA.

    Country: United States

    United States Research PublicationUnited States Research Publication

    AGENCY: United States NIA

    GRANT: AG027476

    ACRONYM: AG

    MEDLINETA: Arch Neurol

    REFSOURCE:

    DATABASENAME:

    ACCESSION NUMBER:

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