Electrophysiological effects of guanosine and MK-801 in a quinolinic acid-induced seizure model

• Published in: Experimental neurology Vol. 221; no. 2; pp. 296 - 306
• Main Authors: Torres, Felipe V., da Silva Filho, Manoel, Antunes, Catiele, Kalinine, Eduardo, Antoniolli, Eduardo, Portela, Luis V.C., Souza, Diogo O., Tort, Adriano B.L.
• Format: Journal Article
• Language: English
• Published: Amsterdam Elsevier Inc 01.02.2010; Elsevier
• Subjects: AED; Analysis of Variance; Animals; Biological and medical sciences; Disease Models, Animal; Dizocilpine Maleate - pharmacology; EEG; Epilepsy; Excitatory Amino Acid Antagonists - pharmacology; Gamma; Guanosine - pharmacology; Headache. Facial pains. Syncopes. Epilepsia. Intracranial hypertension. Brain oedema. Cerebral palsy; Male; Medical sciences; Nervous system (semeiology, syndromes); Neurology; Neuroprotection; Quinolinic Acid; Rats; Rats, Wistar; Seizure; Seizures - chemically induced; Seizures - physiopathology; Spectrum Analysis; Theta; Theta Rhythm - drug effects; AED; Gamma; Neuroprotection; EEG; Epilepsy; Seizure; Theta; Nervous system diseases; Guanosine; Electrophysiology; Electroencephalography; Epilepsy provoked by; Cerebral disorder; Convulsion; Central nervous system disease; Models; Neurological disorder
• ISSN: 0014-4886; 1090-2430; 1090-2430
• DOI: 10.1016/j.expneurol.2009.11.013

Quinolinic acid (QA) is an N-methyl- d-aspartate receptor agonist that also promotes glutamate release and inhibits glutamate uptake by astrocytes. QA is used in experimental models of seizures studying the effects of overstimulation of the glutamatergic system. The guanine-based purines (GBPs), including the nucleoside guanosine, have been shown to modulate the glutamatergic system when administered extracellularly. GBPs were shown to inhibit the binding of glutamate and analogs, to be neuroprotective under excitotoxic conditions, as well as anticonvulsant against seizures induced by glutamatergic agents, including QA-induced seizure. In this work, we studied the electrophysiological effects of guanosine against QA-induced epileptiform activity in rats at the macroscopic cortical level, as inferred by electroencephalogram (EEG) signals recorded at the epidural surface. We found that QA disrupts a prominent basal theta (4–10 Hz) activity during peri-ictal periods and also promotes a relative increase in gamma (20–50 Hz) oscillations. Guanosine, when successfully preventing seizures, counteracted both these spectral changes. MK-801, an NMDA-antagonist used as positive control, was also able counteract the decrease in theta power; however, we observed an increase in the power of gamma oscillations in rats concurrently treated with MK-801 and QA. Given the distinct spectral signatures, these results suggest that guanosine and MK-801 prevent QA-induced seizures by different network mechanisms.