The problem of the relationship between stimulus intensity and kindling effect was studied in three groups of cats with bipolar stimulating electrodes implanted in the right posterior sigmoid gyrus (sensorimotor cortex). Daily stimulation with a 1-sec train of 60-Hz rectangular pulses was carried out in 17 cats over a period of from 27 to 265 days. Group I, 3 cats, was stimulated with a current intensity of 200 microA, peak-to-peak, which was subthreshold for afterdischarges (ADs); 6 animals from group II were stimulated with near-threshold currents (0.8--1.1 mA); and in the 8 animals of the group III, the ADs were evoked by threshold currents of 1.0--1.6 mA. The EEG was recorded from the sensorimotor and visual cortices, hippocampus, caudate nucleus, dentate nucleus, and cerebellar cortex. It was found that the low-current stimulation (200 microV) was not effective in inducing kindling. Near-threshold stimulation (below 1 mA) resulted in the development of bioelectrical epileptic activity in most cats. Threshold stimulation for AD resulted in the development of bioelectrical spontaneous activity and in an increase in the duration of ADs, as well as in generalized tonic-clonic seizures during cortical stimulations, in the majority of cats. Differences in hippocampal and neocortical kindling in cats are discussed in terms of ADs and seizure development. It was found that (1) a longer time was required for neocortical than for hippocampal kindling (3--10 weeks), and (2) there was greater variability in the effects of neocortical kindling. Secondary generalized seizures developed in the group with threshold stimulation for AD and were preceded by an increase in the number of ADs. The interictal epileptic activity developed in some cats in the absence of ADs.
Alumina cream epileptic focus was established in the right sensorimotor cortex in 20 split-brain cats (partial or complete). EEG and behavioral observations were made in a period ranging from 24 to 836 days. Four types of EEG changes after alumina cream injection were differentiated. These types could be related to the direct effects of brain damage and to development of epilepsy. Spikes and sharp waves and paroxysmal discharges (focal and multifocal) were observed in about 60% of the cats. Clinical seizures developed in about the same percentage of the animals. These values are below those reported for cats with intact interhemispheric commissures. Diphenylhydantoin (DPH) was given orally in a daily dose of up to 15 mg/kg body weight in 9 animals with developed epileptic EEG activity. Five of them had epileptic seizures. DPH was introduced not earlier than 1.5 months after intracortical alumina cream injection. The plasma level of DPH varied between 7-20 mug/ml. This dose produced chronic symptoms of intoxication. Neither EEG changes nor clinical seizures were entirely controlled by this drug. Additional doses of Relanium (diazepam), and phenobarbital were necessary to stop generalized seizures or status epilepticus.
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