Effects of AWD 140-190 on stimulus-induced field potentials and on different patterns of epileptiform activity induced by low calcium or low magnesium in rat entorhinal cortex hippocampal slices
Autor: | Uwe Heinemann, V. Armand, C. Rundfeldt |
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Rok vydání: | 1997 |
Předmět: |
Proline
Morpholines medicine.medical_treatment Stimulation In Vitro Techniques Stimulus (physiology) Hippocampal formation Hippocampus medicine Extracellular Animals Entorhinal Cortex Magnesium Rats Wistar Evoked Potentials Epilepsy Chemistry Low magnesium Entorhinal cortex Electric Stimulation Rats Anticonvulsant Neurology Cortical spreading depression Potassium Biophysics Anticonvulsants Calcium Neurology (clinical) Neuroscience |
Zdroj: | Epilepsy Research. 29:59-69 |
ISSN: | 0920-1211 |
DOI: | 10.1016/s0920-1211(97)00066-1 |
Popis: | AWD 140-190 a potent new anticonvulsant was tested on several types of epileptiform activities in entorhinal cortex hippocampal slices. AWD 140-190 suppressed completely and in a dose-dependent manner spontaneous seizure-like events induced by lowering extracellular Ca2+. In the low magnesium model, AWD 140-190 applied with 200 microM reduced recurrent short discharges in area CA1 by 48.1 +/- 14.7%, while in the entorhinal cortex seizure-like events were not depressed. Late recurrent discharges were increased in frequency to 213.8 +/- 78.1 and reduced in amplitude by 50.1 +/- 14.4%. Responses to paired pulse stimuli with intervals ranging from 20 to 150 ms were reduced both with alvear and stratum radiatum stimulation. Decreases in [Ca2+]0 and associated slow field potentials evoked by repetitive stimulation of stratum radiatum were also depressed in a dose-dependent manner. AWD 140-190 also reduced stimulus-induced rises in [K+]0. AWD 140-190 200 microM diminished the amplitude of slow field potentials observed during high K(+)-induced spreading depression by about 17% in CA1 and 34% in entorhinal cortex without any significant effect on SD-associated rises in [K+]0. These results suggest that AWD 140-190 has an anticonvulsant effect presumably by interfering with repetitive generation of action potentials. AWD 140-190 may also possess modulatory effects on glial cells as suggested by the strong depression of SD-associated slow negative potential shifts. |
Databáze: | OpenAIRE |
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