Assessing functional outcomes following intracerebral hemorrhage in rats

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    Abstract

    Translational neuroprotective and drug development studies need to be gauged against well-characterized functional outcomes, including motor, sensory and cognitive domains. Since intracerebral hemorrhage (ICH) causes dramatic neurological and cognitive deficits in humans, we hypothesized that ICH would result in prolonged motor-sensory and learning/memory deficits in rats. Neurological tests of sensorimotor functions were performed before ICH, 1-3 days and 10 weeks after ICH. Water maze, open field, and rotarod performance was tested 2 and 8 weeks after ICH. Early neurological evaluations revealed significant deficits, with almost full recovery by 10 weeks. The water maze revealed significant learning (but not motor) deficits at 2 weeks, but by 8 weeks, the learning deficits had diminished and significant motor deficits had emerged, coinciding with a drop in activity. The injured hemisphere showed significant atrophy at sacrifice. Therefore, ICH produced detectable cognitive and motor deficits in rats that evolved over a 10-week period, and thereby provides a suitable baseline for analysis of future therapeutic interventions following hemorrhagic stroke. © 2009 Elsevier B.V. All rights reserved.
    Original languageEnglish
    Pages (from-to)148-157
    Number of pages10
    JournalBrain Research
    Volume1280
    DOIs
    StatePublished - Jul 14 2009

    ASJC Scopus Subject Areas

    • General Neuroscience
    • Molecular Biology
    • Clinical Neurology
    • Developmental Biology

    Keywords

    • Collagenase
    • Hemorrhage
    • Learning
    • Memory
    • Motor
    • Body Weight
    • Intracranial Hemorrhages/complications
    • Learning Disabilities/etiology
    • Rats
    • Male
    • Motor Activity
    • Rats, Sprague-Dawley
    • Recovery of Function
    • Neuropsychological Tests
    • Brain/pathology
    • Animals
    • Maze Learning
    • Analysis of Variance
    • Movement Disorders/etiology
    • Time Factors
    • Memory Disorders/etiology
    • Aging

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