The long-range goal of this project is a comprehensive study of the effects of hypoxia on central nervous tissue of mammals. Since the objective is the effect of oxygen deprivation, separated from indirect effects caused by systemic changes, in vitro preparations are used in many experiments. Recordings from the brains of anesthetized rats will be used to compare effects observed in vitro to the responses of brain in situ. Cerebral hypoxia leads to: I. reversible failure of synaptic functions; II. irreversible loss of function; III. delayed deterioration after initial recovery following reoxygenation. A set of hypotheses has been developed, in part from the literature, and in part from the results of past work in our laboratory concerning the mechanism of this sequence of processes. This proposal is for the testing of key elements of the hypothetical hypoxic process. Experiments planned for this budget period fall into six sub-projects: 1.Hypoxic conduction failure in spinal presynaptic terminals in isolated mouse spinal cord. 2.The changes of EPSP, threshold, membrane potential and membrane current in the reversible phase of hypoxia in hippocampal tissue slices. 3.Intracellular recordings during and after hypoxic and normoxic spreading depression (SD) in hippocampal tissue slices. 4.Reversibility of prolonged, K+-induced SD in cerebral cortex and in hippocampus in the brain of anesthetized rats. 5.Comparison of hypoxic changes in CA1, CA3 and in fascia dentata (FD) of the brain of anesthetized rats. 6.Delayed post-hypoxic changes in hippocampal tissue slices.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
2R01NS018670-07A2
Application #
3398710
Study Section
Neurology A Study Section (NEUA)
Project Start
1982-07-01
Project End
1992-11-30
Budget Start
1989-12-01
Budget End
1990-11-30
Support Year
7
Fiscal Year
1990
Total Cost
Indirect Cost
Name
Duke University
Department
Type
Schools of Medicine
DUNS #
071723621
City
Durham
State
NC
Country
United States
Zip Code
27705
Fayuk, Dmitriy; Aitken, Peter G; Somjen, George G et al. (2002) Two different mechanisms underlie reversible, intrinsic optical signals in rat hippocampal slices. J Neurophysiol 87:1924-37
Muller, M (2000) Effects of chloride transport inhibition and chloride substitution on neuron function and on hypoxic spreading-depression-like depolarization in rat hippocampal slices. Neuroscience 97:33-45
Borgdorff, A J; Somjen, G G; Wadman, W J (2000) Two mechanisms that raise free intracellular calcium in rat hippocampal neurons during hypoosmotic and low NaCl treatment. J Neurophysiol 83:81-9
Somjen, G G; Muller, M (2000) Potassium-induced enhancement of persistent inward current in hippocampal neurons in isolation and in tissue slices. Brain Res 885:102-10
Somjen, G G (2000) Enhancement of persistent sodium current by internal fluorescence in isolated hippocampal neurons. Brain Res 885:94-101
Bahar, S; Fayuk, D; Somjen, G G et al. (2000) Mitochondrial and intrinsic optical signals imaged during hypoxia and spreading depression in rat hippocampal slices. J Neurophysiol 84:311-24
Kager, H; Wadman, W J; Somjen, G G (2000) Simulated seizures and spreading depression in a neuron model incorporating interstitial space and ion concentrations. J Neurophysiol 84:495-512
Muller, M; Somjen, G G (2000) Na(+) and K(+) concentrations, extra- and intracellular voltages, and the effect of TTX in hypoxic rat hippocampal slices. J Neurophysiol 83:735-45
Muller, M; Somjen, G G (2000) Na(+) dependence and the role of glutamate receptors and Na(+) channels in ion fluxes during hypoxia of rat hippocampal slices. J Neurophysiol 84:1869-80
Balestrino, M; Young, J; Aitken, P (1999) Block of (Na+,K+)ATPase with ouabain induces spreading depression-like depolarization in hippocampal slices. Brain Res 838:37-44

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