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Changes in neuropeptide Y protein expression following photothrombotic brain infarction and epileptogenesis.

Changes in neuropeptide Y protein expression following photothrombotic brain infarction and epileptogenesis. Research Abstract Details 

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  • Changes in neuropeptide Y protein expression following photothrombotic brain infarction and epileptogenesis. Abstract Text:

    elena a kharlamovElena A Kharlamov,alexander kharlamovAlexander Kharlamov,kevin m kellyKevin M Kelly,

    This study characterized morphological changes in the cortex and hippocampus of Sprague-Dawley rats following photothrombotic infarction and epileptogenesis with emphasis on the distribution of neuropeptide Y (NPY) expression. Animals were lesioned in the left sensorimotor cortex and compared with age-matched naive and sham-operated controls by immunohistochemical techniques at 1, 3, 7, and 180 days post-lesioning (DPL). NPY immunostaining was assessed by light microscopy and quantified by the optical fractionator technique using unbiased stereological methods. At 1, 3, and 7 DPL, the number of NPY-positive somata in the lesioned cortex was increased significantly compared to controls and the contralateral cortex. At 180 DPL, lesioned epileptic animals with frequent seizure activity demonstrated significant increases of NPY expression in the cortex, CA1, CA3, hilar interneurons, and granule cells of the dentate gyrus. In addition to NPY immunostaining, neuronal degeneration, cell death/cell loss, and astroglial response were assessed with cell-specific markers. Nissl and NeuN staining showed reproducible infarctions at each investigated time point. FJB-positive somata were most abundant in the infarct core at 1 DPL, decreased markedly at 3 DPL, and virtually absent by 7 DPL. Activated astroglia were detected in the cortex and hippocampus following lesioning and the development of seizure activity. In summary, NPY protein expression and morphological changes following cortical photothrombosis were time-, region-, and pathologic state-dependent. Alterations in NPY expression may reflect reactive or compensatory responses of the rat brain to acute infarction and to the development and expression of epileptic seizures.

    Changes in neuropeptide Y protein expression following photothrombotic brain infarction and epileptogenesis. Publishing Authors By Initials

    ea kharlamovEA Kharlamov,a kharlamovA Kharlamov,km kellyKM Kelly,

    For similar genetic processes: gene expression regulation: up-regulation research abstracts see: genetic processes: gene expression regulation: up-regulation research

    PUBMED ID PMID:

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    Changes in neuropeptide Y protein expression following photothrombotic brain infarction and epileptogenesis. Journal Published:

    PUBLICATION TYPE: Research Support, N.I.H., Extr

    Journal: Brain research

    VOLUME: 1127

    Page Numbers: 151-62

    Journal Abbreviation: Brain Res.

    ISSN: 0006-8993

    DAY: 22

    MONTH: 11

    YEAR: 2006

    Changes in neuropeptide Y protein expression following photothrombotic brain infarction and epileptogenesis. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 45503

    Changes in neuropeptide Y protein expression following photothrombotic brain infarction and epileptogenesis. Keywords Mesh Terms:

    KEYWORDS: Up-Regulation

    MESH TERMS: physiology

    Chemical & Substance for Abstract: Changes in neuropeptide Y protein expression following photothrombotic brain infarction and epileptogenesis. Information

    Substance Name: fluoro jade

    Registry Number: 0

    Grant and Affiliation Information for Changes in neuropeptide Y protein expression following photothrombotic brain infarction and epileptogenesis.

    AFFILIATION: Department of Neurology, Allegheny-Singer Research Institute, Allegheny General Hospital, Pittsburgh, PA, USA.

    Country: Netherlands

    Netherlands Research PublicationNetherlands Research Publication

    AGENCY: United States NINDS

    GRANT: R01NS04601

    ACRONYM: NS

    MEDLINETA: Brain Res

    REFSOURCE:

    DATABASENAME:

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