TY - JOUR
T1 - Brain Synapses
T2 - An in Vitro Model for the Study of Seizures
AU - Escueta, Antonio V.
AU - Appel, Stanley H.
PY - 1972/2
Y1 - 1972/2
N2 - Electrophysiological studies have recently emphasized abnormal synaptic function as an important factor in the generation of seizure discharges. To further delineate these abnormalities, synaptic terminals (synaptosomes) were isolated from brains of animals with seizures. After repeated electroconvulsions (a model used to study the effects of seizures), the level of potassium decreased while that of sodium increased within synaptic terminals because of an enhanced downhill movement of cations. In epileptogenic foci of freezing lesions (a model used to study epileptogenesis), K influx mediated by the Na-K pump was markedly impaired with synaptic terminals. Both pathologic processes in membrane function were corrected by diphenylhydantoin through its stimulation of the Na-K pump. In epileptogenic foci, diphenylhydantoin may also have a direct action on the synapse membrane, apart from its effects on the Na-K pump.
AB - Electrophysiological studies have recently emphasized abnormal synaptic function as an important factor in the generation of seizure discharges. To further delineate these abnormalities, synaptic terminals (synaptosomes) were isolated from brains of animals with seizures. After repeated electroconvulsions (a model used to study the effects of seizures), the level of potassium decreased while that of sodium increased within synaptic terminals because of an enhanced downhill movement of cations. In epileptogenic foci of freezing lesions (a model used to study epileptogenesis), K influx mediated by the Na-K pump was markedly impaired with synaptic terminals. Both pathologic processes in membrane function were corrected by diphenylhydantoin through its stimulation of the Na-K pump. In epileptogenic foci, diphenylhydantoin may also have a direct action on the synapse membrane, apart from its effects on the Na-K pump.
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U2 - 10.1001/archinte.1972.00320020177015
DO - 10.1001/archinte.1972.00320020177015
M3 - Article
C2 - 4258091
AN - SCOPUS:0015290514
SN - 0003-9926
VL - 129
SP - 333
EP - 344
JO - Archives of Internal Medicine
JF - Archives of Internal Medicine
IS - 2
ER -