Interaction between free radicals and excitatory amino acids in the formation of ischemic brain edema in rats.
- 1 July 1991
- journal article
- research article
- Published by Wolters Kluwer Health in Stroke
- Vol. 22 (7) , 915-921
- https://doi.org/10.1161/01.str.22.7.915
Abstract
Both oxygen free radicals and excitatory amino acids have been implicated as important cellular toxins in ischemic brain. Recent in vitro studies suggest that there may be a mutual interaction between these two mediators. We explored the relation between oxygen free radicals and excitatory amino acids in the development of ischemic brain edema in vivo. Male Sprague-Dawley rats were treated with the free radical scavenger dimethylthiourea 1 hour before ischemia or with the excitotoxin antagonist MK-801 30 minutes before ischemia produced by occlusion of the middle cerebral artery. Groups of seven or eight animals were treated with vehicle, low-dose (375 mg/kg) dimethylthiourea, high-dose (750 mg/kg) dimethylthiourea, low-dose (0.5 mg/kg) MK-801, high-dose (2.0 mg/kg) MK-801, or both high-dose dimethylthiourea and low-dose MK-801. After 4 hours of ischemia, brain water content was determined. In eight vehicle-treated controls, mean +/- SEM water content of tissue in the center of the ischemic zone was 83.29 +/- 0.18%. A significant reduction of brain edema was observed in all drug-treated groups: for example, 50.2% (p less than 0.001) in the high-dose dimethylthiourea group, 53.7% (p less than 0.001) in the low-dose MK-801 group, and 66.4% (p less than 0.001) in the combined dimethylthiourea and MK-801 group. Combined treatment with dimethylthiourea and MK-801 provided no significant additive effect over that resulting from treatment with MK-801 alone.(ABSTRACT TRUNCATED AT 250 WORDS)Keywords
This publication has 41 references indexed in Scilit:
- 21-Aminosteroids attenuate excitotoxic neuronal injury in cortical cell culturesNeuron, 1990
- Protection by NMDA Antagonists against Selective Cell Loss following Transient IschaemiaJournal of Cerebral Blood Flow & Metabolism, 1990
- Ischemic Damage in Hippocampal CA1 is Dependent on Glutamate Release and Intact Innervation from CA3Journal of Cerebral Blood Flow & Metabolism, 1989
- The Neuroprotective Action of Ketamine and MK-801 after Transient Cerebral Ischemia in RatsAnesthesiology, 1988
- NMDA receptors activate the arachidonic acid cascade system in striatal neuronsNature, 1988
- Small Differences in Intraischemic Brain Temperature Critically Determine the Extent of Ischemic Neuronal InjuryJournal of Cerebral Blood Flow & Metabolism, 1987
- Mechanism of Kainate Toxicity to Cerebellar Neurons In Vitro Is Analogous to Reperfusion Tissue InjuryJournal of Neurochemistry, 1987
- Excitotoxity and the NMDA receptorTrends in Neurosciences, 1987
- Elevation of the Extracellular Concentrations of Glutamate and Aspartate in Rat Hippocampus During Transient Cerebral Ischemia Monitored by Intracerebral MicrodialysisJournal of Neurochemistry, 1984
- Prevention of granulocyte-mediated oxidant lung injury in rats by a hydroxyl radical scavenger, dimethylthiourea.Journal of Clinical Investigation, 1984