Local generation of fast ripples in epileptic brain.
|Title||Local generation of fast ripples in epileptic brain.|
|Publication Type||Journal Article|
|Year of Publication||2002|
|Authors||Bragin, A, Mody I, Wilson CL, Engel J|
|Journal||The Journal of neuroscience : the official journal of the Society for Neuroscience|
|Date Published||2002 Mar 1|
|Keywords||Action Potentials, Animals, Biological Clocks, Brain, Brain Mapping, Chronic Disease, Dentate Gyrus, Disease Models, Animal, Electric Stimulation, Entorhinal Cortex, Epilepsy, Evoked Potentials, Feedback, GABA Antagonists, Hippocampus, Kainic Acid, Male, Microelectrodes, Neural Inhibition, Perforant Pathway, Rats, Rats, Sprague-Dawley, Reaction Time|
Aperiodic high-frequency oscillations (>100 Hz) reflect a short-term synchronization of neuronal electrical activity. It has been shown in the epileptic brain that spontaneous oscillations in the frequency range of 250-600 Hz reflect action potential population bursts of synchronously discharging neuronal clusters. These oscillations occur in the early stages of epileptogenesis in areas adjacent to the brain lesion and may trigger the formation of seizure-generating neuronal networks. We studied the extent of the area generating oscillations in the frequency range of 250-600 Hz [fast ripples (FRs)] in intrahippocampal kainic acid-treated rats with spontaneous seizures, by analyzing voltage versus depth profiles of FRs in hippocampal and parahippocampal areas in freely moving animals and by spatial mapping in hippocampal slice preparations in vitro. The strength of inhibition was compared in areas with and without FRs using a paired-pulse paradigm. The extent of the areas generating FRs did not exceed 1 mm(3). The areas generating FRs became broader after the application of the GABA(A) receptor antagonist bicuculline. Paired-pulse fast inhibition at 15-30 msec intervals was similar in areas generating FRs and areas not generating FRs. Our data illustrate that hypothesized clusters of highly interconnected neurons are capable of overcoming interneuron feedback inhibition, resulting in generation of epileptiform bursts, eventually leading to seizure activity.
|Alternate Journal||J. Neurosci.|