Applications of quantitative measurements for assessing glutamate neurotoxicity.
- 1 June 1988
- journal article
- research article
- Published by Proceedings of the National Academy of Sciences in Proceedings of the National Academy of Sciences
- Vol. 85 (11) , 4071-4074
- https://doi.org/10.1073/pnas.85.11.4071
Abstract
The role of the N-methyl-D-aspartate receptor channel in glutamate neurotoxicity was investigated in cultured hippocampal neurons of the CA1 region. An equation, the survival function, was developed to quantify the effects of putative modulators of neurotoxicity. 2-Amino-5-phosphonovaleric acid (30 .mu.M) reduced the neuronal sensitivity to glutamate by a factor > 20, whereas glycine (1 .mu.M) enhanced it by a factor of 7.5 .+-. 2.5. Neurons were protected by increasing Mg2+ concentrations in a predictable way based on the ion''s ability to block the N-methyl-D-aspartate channel. These findings provide a quantitative basis for the assessment of various neuroprotective agents and add further support to the hypothesis that the N-methyl-D-aspartate channel is central to glutamate neurotoxicity.This publication has 32 references indexed in Scilit:
- Glycine potentiates the NMDA response in cultured mouse brain neuronsNature, 1987
- Glutamate activates multiple single channel conductances in hippocampal neuronsNature, 1987
- Glutamic Acid as a Putative Transmitter of the Interhemispheric Corticocortical Connections in the RatJournal of Neurochemistry, 1986
- Mechanisms of MemoryScience, 1986
- Neurotoxicity of excitatory amino acid receptor agonists in rat cerebellar slices: Dependence on calcium concentrationNeuroscience Letters, 1986
- NMDA-receptor activation increases cytoplasmic calcium concentration in cultured spinal cord neuronesNature, 1986
- Glutamate neurotoxicity in cortical cell culture is calcium dependentNeuroscience Letters, 1985
- Magnesium gates glutamate-activated channels in mouse central neuronesNature, 1984
- Glutamate: A Neurotransmitter in Mammalian BrainJournal of Neurochemistry, 1984
- Synaptic Activity Mediates Death of Hypoxic NeuronsScience, 1983