Abstract
The benzodiazepine antagonists Ro 15-1788 and CGS 8216 blocked the clonic and tonic convulsions elicited by 3-carbomethoxy-beta-carboline (beta-CCM). The PD50 values for Ro 15-1788, CGS 8216, and diazepam were: 2.0, 0.6, and 2.0 mg/kg, respectively. Neither Ro 15-1788 nor CGS 8216 potentiated the effect of a threshold convulsant dose of beta-CCM. Moreover, these benzodiazepine antagonists neither attenuated nor potentiated the tremorigenic actions of another beta-carboline, harmaline. Diazepam, however, considerably reduced the tremorigenic actions of this drug.
MeSH terms
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Animals
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Benzodiazepinones / pharmacology*
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Carbolines / antagonists & inhibitors*
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Convulsants / antagonists & inhibitors*
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Diazepam / pharmacology*
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Dose-Response Relationship, Drug
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Flumazenil
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Harmaline / pharmacology
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Indoles / antagonists & inhibitors*
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Male
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Mice
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Pyrazoles / pharmacology*
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Seizures / chemically induced
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Seizures / prevention & control*
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Tremor / chemically induced
Substances
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Benzodiazepinones
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Carbolines
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Convulsants
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Indoles
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Pyrazoles
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Flumazenil
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2-phenylpyrazolo(4,3-c)quinolin-3(5H)-one
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Harmaline
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beta-carboline-3-carboxylic acid methyl ester
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Diazepam