Distribution and time course of the occurrence of "dark" neurons were compared with the EEG activity and behavior of rats during 4-aminopyridine (4-AP) induced epileptic seizures.A crystal of the K + channel blocker 4-AP (0.5 mg/kg) was placed onto the exposed parietooccipital cortex of Halothane-anesthetized rats for 40 min. Thereafter, the anesthesia was discontinued and the behavioral signs of the epileptic seizure activity were observed. The
IntroductionUnderstanding of the development and generalization of the epileptic seizure activity and the accompanying changes in the molecular structure of the brain cells are great challenges in neurology and neuroscience. It is well known that epileptic convulsions are the end-result of the hyperexcitability of several excitatory neuronal circuits and of the spread of the seizure activity over the whole cerebrum. In addition to the excitatory circuits, the inhibitory interneuron networks are also involved in the progression of epileptic seizure activity (Benardo, 1997;Mody et al., 1992). The epileptic activity causes sustained depolarization in both excitatory and inhibitory neurons with a concomitant elevation of intracellular Ca ++ , in turn, results in both pathological and protective changes in the cellular protein composition (Ogita et al., 2005).The seizure-related, significantly elevated intracellular Ca ++ -concentration is a cellular stress which, on the morphological level, can be manifested in the compaction of the ultrastructure of neurons. Such neurons are traditionally