strychnine and gamma-hydroxy-gamma-ethyl-gamma-phenylbutyramide

strychnine has been researched along with gamma-hydroxy-gamma-ethyl-gamma-phenylbutyramide* in 1 studies

Other Studies

1 other study(ies) available for strychnine and gamma-hydroxy-gamma-ethyl-gamma-phenylbutyramide

Article	Year
Neurophysiological and neurochemical studies on the action of the anticonvulsant gamma-hydroxy, gamma-ethyl, gamma-phenyl-butyramide. Epilepsia, 1979, Volume: 20, Issue:2 The effect of gamma-hydroxy, gamma-ethyl, gamma-phenyl-butyramide (HEPB) on afterdischarges produced by hippocampal stimulation in cats was studied. HEPB notably diminished the duration of afterdischarges and in some cats blocked their propagation into the substantia nigra and the amygdala. HEPB treatment also antagonized the enhancement of afterdischarge duration produced by subconvulsive doses of bicuculline, whereas treatment with diphenylhydantoin strongly potentiated this effect of bicuculline. The intracisternal injection of HEPB or gamma-aminobutyric acid (GABA) in mice resulted in a potentiation of strychnine-induced convulsions. On the other hand, neurochemical experiments in mouse brain cortex slices and in synaptosomes demonstrated that HEPB did not affect the high affinity uptake of [3H] GABA, its spontaneous or Ca2+ dependent release stimulated by depolarizing K+ concentrations, and its Na+ independent binding to synaptic plasma membranes. Topics: Amygdala; Animals; Anticonvulsants; Bicuculline; Brain; Cats; Cerebral Cortex; Drug Synergism; Electric Stimulation; Evoked Potentials; gamma-Aminobutyric Acid; Hippocampus; Mice; Phenylbutyrates; Phenytoin; Potassium; Seizures; Strychnine; Substantia Nigra	1979

Article

Year

Neurophysiological and neurochemical studies on the action of the anticonvulsant gamma-hydroxy, gamma-ethyl, gamma-phenyl-butyramide.

Epilepsia, 1979, Volume: 20, Issue:2

The effect of gamma-hydroxy, gamma-ethyl, gamma-phenyl-butyramide (HEPB) on afterdischarges produced by hippocampal stimulation in cats was studied. HEPB notably diminished the duration of afterdischarges and in some cats blocked their propagation into the substantia nigra and the amygdala. HEPB treatment also antagonized the enhancement of afterdischarge duration produced by subconvulsive doses of bicuculline, whereas treatment with diphenylhydantoin strongly potentiated this effect of bicuculline. The intracisternal injection of HEPB or gamma-aminobutyric acid (GABA) in mice resulted in a potentiation of strychnine-induced convulsions. On the other hand, neurochemical experiments in mouse brain cortex slices and in synaptosomes demonstrated that HEPB did not affect the high affinity uptake of [3H] GABA, its spontaneous or Ca2+ dependent release stimulated by depolarizing K+ concentrations, and its Na+ independent binding to synaptic plasma membranes.

Topics: Amygdala; Animals; Anticonvulsants; Bicuculline; Brain; Cats; Cerebral Cortex; Drug Synergism; Electric Stimulation; Evoked Potentials; gamma-Aminobutyric Acid; Hippocampus; Mice; Phenylbutyrates; Phenytoin; Potassium; Seizures; Strychnine; Substantia Nigra

1979