This program project focuses research clinicians and basic neurobiology investigators on the analysis and modeling of human epileptogenic tissue. The surgically resected tissue will come from two well-defined human seizure disorders, temporal lobe epilepsy associated with medial temporal sclerosis (medial temporal lobe epilepsy (MTLE), and epilepsy associated with chronic tumors (tumor associated epilepsy (TAE). Experimental neurobiological techniques will be used to address specific hypotheses relating to the electrophysiology, anatomy, and biochemistry of the hippocampus and parahippocampus in MTLE and of the tumor with surrounding cortex in TAE. The program is divided into three major sections. The first defines the tissues' electrophysiological characteristics using depth electrodes and intraoperative recording and stimulating techniques (Project 1, S. Spencer). This same tissue is then studied in slice preparations asking similar questions at an intracellular and network level (Project 2, A. Williamson). The second section uses immunohistochemical, autoradiographical, and molecular techniques to characterize structure (Project 3, N. de Lanerolle). Data from all three projects is correlated and compared with a heat-kindled rat model (Project 3, N. de Lanerolle). The third section studies the neurobiology of ion-regulating proteins in the tissue of these two human focal epileptic conditions attempting to understand what cellular (particularly glial) events predispose to neuronal death and resultant excitability and more specifically, Dr. A. Cornell-Bell (Project 5) will characterize glial Ca++ physiology and glutamate pharmacology in human and animal tissue using optical imaging techniques.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Program Projects (P01)
Project #
5P01NS030619-03
Application #
2268594
Study Section
Neurological Disorders Program Project Review A Committee (NSPA)
Project Start
1993-02-01
Project End
1998-01-31
Budget Start
1995-02-01
Budget End
1996-01-31
Support Year
3
Fiscal Year
1995
Total Cost
Indirect Cost
Name
Yale University
Department
Surgery
Type
Schools of Medicine
DUNS #
082359691
City
New Haven
State
CT
Country
United States
Zip Code
06520
van den Pol, A N; Spencer, D D (2000) Differential neurite growth on astrocyte substrates: interspecies facilitation in green fluorescent protein-transfected rat and human neurons. Neuroscience 95:603-16
Jiang, W; Duong, T M; de Lanerolle, N C (1999) The neuropathology of hyperthermic seizures in the rat. Epilepsia 40:5-19
Telfeian, A E; Spencer, D D; Williamson, A (1999) Lack of correlation between neuronal hyperexcitability and electrocorticographic responsiveness in epileptogenic human neocortex. J Neurosurg 90:939-45
O'Connor, E R; Sontheimer, H; Spencer, D D et al. (1998) Astrocytes from human hippocampal epileptogenic foci exhibit action potential-like responses. Epilepsia 39:347-54
de Lanerolle, N C; Eid, T; von Campe, G et al. (1998) Glutamate receptor subunits GluR1 and GluR2/3 distribution shows reorganization in the human epileptogenic hippocampus. Eur J Neurosci 10:1687-703
Haak, L L; Heller, H C; van den Pol, A N (1997) Metabotropic glutamate receptor activation modulates kainate and serotonin calcium response in astrocytes. J Neurosci 17:1825-37
von Campe, G; Spencer, D D; de Lanerolle, N C (1997) Morphology of dentate granule cells in the human epileptogenic hippocampus. Hippocampus 7:472-88
Brines, M L; Sundaresan, S; Spencer, D D et al. (1997) Quantitative autoradiographic analysis of ionotropic glutamate receptor subtypes in human temporal lobe epilepsy: up-regulation in reorganized epileptogenic hippocampus. Eur J Neurosci 9:2035-44
de Lanerolle, N C; Williamson, A; Meredith, C et al. (1997) Dynorphin and the kappa 1 ligand [3H]U69,593 binding in the human epileptogenic hippocampus. Epilepsy Res 28:189-205
Van Den Pol, A N; Obrietan, K; Belousov, A (1996) Glutamate hyperexcitability and seizure-like activity throughout the brain and spinal cord upon relief from chronic glutamate receptor blockade in culture. Neuroscience 74:653-74

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