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Enhanced Phosphodiestric Breakdown of Phosphatidylinositol Bisphosphate After Experimental Brain Injury

Authors

  • M. Renuka Prasad,

    Corresponding author
    1. Departments of Surgery, Anatomy, and Neurobiology, University of Kentucky Chandler Medical Center, Lexington, Kentucky, U.S.A.
      Address correspondence and reprint requests to Dr. M. R. Prasad at Division of Neurosurgery, Department of Surgery, University of Kentucky Chandler Medical Center, Lexington, KY 40536-0084, U.S.A.
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  • H. S. Dhillon,

    1. Departments of Surgery, Anatomy, and Neurobiology, University of Kentucky Chandler Medical Center, Lexington, Kentucky, U.S.A.
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  • T. Carbary,

    1. Departments of Surgery, Anatomy, and Neurobiology, University of Kentucky Chandler Medical Center, Lexington, Kentucky, U.S.A.
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  • R. J. Dempsey,

    1. Departments of Surgery, Anatomy, and Neurobiology, University of Kentucky Chandler Medical Center, Lexington, Kentucky, U.S.A.
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  • S. W. Scheff

    1. Departments of Surgery, Anatomy, and Neurobiology, University of Kentucky Chandler Medical Center, Lexington, Kentucky, U.S.A.
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Address correspondence and reprint requests to Dr. M. R. Prasad at Division of Neurosurgery, Department of Surgery, University of Kentucky Chandler Medical Center, Lexington, KY 40536-0084, U.S.A.

Abstract

Abstract: Regional levels of lactate and inositol 1,4,5-trisphosphate (IP3), a cellular second messenger of the excitatory neurotransmitter system, were measured after lateral fluid percussion (FP) brain injury in rats. At 5 min postinjury, tissue lactate concentrations were significantly elevated in the cortices and hippocampi of both the ipsilateral and contralateral hemispheres. By 20 min postinjury, lactate concentrations were elevated only in the cortices and hippocampus of the ipsilateral hemisphere. Whereas the IP3 concentrations were elevated in the hippocampi of the ipsilateral and contralateral hemisphere and in the cortex of ipsilateral hemisphere at 5 min postinjury, no elevation in these sites was found at 20 min postinjury. Histologic analysis revealed neuronal damage in the cortex and CA3 regions of hippocampus ipsilateral to the injury at 24 h postinjury. The present results suggest activation of the phosphoinositide signal transduction pathway at the onset of injury and of a possible requirement of early persistent metabolic dysfunction (>20 min) such as the lactate accumulation in the delayed neuronal damage.

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