Extracellular concentrations of the brain metabolite quinolinic acid, an endogenous excitotoxin, were monitored by microdialysis in rat neostriatum and hippocampus/cortex during and following a 30-min period of insulin-induced hypoglycaemia. During hypoglycaemia-induced isoelectricity, extracellular levels of quinolinic acid in the striatum (basal value, 1.1 ± 0.3 pmol per 30-μl fraction) were elevated 1.7 times as compared to the control period. Thirty to ninety minutes following hypoglycaemia a significant increase in extracellular quinolinic acid to 2.2 times basal level was noted. After 2 h recovery, the beginning of neuronal necrosis was observed in the dorsolateral striatum. Implantation of the dialysis probe did not influence the ext...
Although the involvement of oxidative mechanisms in the cytotoxicity of excitatory amino acids has b...
Although the involvement of oxidative mechanisms in the cytotoxicity of excitatory amino acids has b...
Rats were exposed to insulin-induced hypoglycemia resulting in periods of cerebral isoelectricity ra...
Extracellular concentrations of the brain metabolite quinolinic acid, an endogenous excitotoxin, wer...
The excitotoxic hypothesis of Huntington's disease pathogenesis suggests that selective striatal neu...
Excitotoxicity plays a role in the cell death observed in acute forms of neuronal injury including s...
Abstract: An involvement of excitatory amino acid (EAA) transmitter–receptor interactions in the dev...
AbstractExtracellular fluid levels of the neurotoxin quinolinic acid in the corpus striatum of rats,...
Profound hypoglycemia causing the disappearance of spontaneous EEG activity was induced by insulin i...
Abstract: In the cerebral cortices of rats, during insulininduced hypoglycemia, changes in the conce...
Abstract: In the cerebral cortices of rats, during insulininduced hypoglycemia, changes in the conce...
Excessive activation of NMDA glutamate receptors and the resulting loss of intracellular Ca(2+) home...
Injection of excitotoxins, such as quinolinic acid (QA), into the striatum has been extensively used...
Excessive activation of NMDA glutamate receptors and the resulting loss of intracellular Ca(2+) home...
Although the involvement of oxidative mechanisms in the cytotoxicity of excitatory amino acids has b...
Although the involvement of oxidative mechanisms in the cytotoxicity of excitatory amino acids has b...
Although the involvement of oxidative mechanisms in the cytotoxicity of excitatory amino acids has b...
Rats were exposed to insulin-induced hypoglycemia resulting in periods of cerebral isoelectricity ra...
Extracellular concentrations of the brain metabolite quinolinic acid, an endogenous excitotoxin, wer...
The excitotoxic hypothesis of Huntington's disease pathogenesis suggests that selective striatal neu...
Excitotoxicity plays a role in the cell death observed in acute forms of neuronal injury including s...
Abstract: An involvement of excitatory amino acid (EAA) transmitter–receptor interactions in the dev...
AbstractExtracellular fluid levels of the neurotoxin quinolinic acid in the corpus striatum of rats,...
Profound hypoglycemia causing the disappearance of spontaneous EEG activity was induced by insulin i...
Abstract: In the cerebral cortices of rats, during insulininduced hypoglycemia, changes in the conce...
Abstract: In the cerebral cortices of rats, during insulininduced hypoglycemia, changes in the conce...
Excessive activation of NMDA glutamate receptors and the resulting loss of intracellular Ca(2+) home...
Injection of excitotoxins, such as quinolinic acid (QA), into the striatum has been extensively used...
Excessive activation of NMDA glutamate receptors and the resulting loss of intracellular Ca(2+) home...
Although the involvement of oxidative mechanisms in the cytotoxicity of excitatory amino acids has b...
Although the involvement of oxidative mechanisms in the cytotoxicity of excitatory amino acids has b...
Although the involvement of oxidative mechanisms in the cytotoxicity of excitatory amino acids has b...
Rats were exposed to insulin-induced hypoglycemia resulting in periods of cerebral isoelectricity ra...