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J Neurochem ; 40(2): 514-21, 1983 Feb.
Article in English | MEDLINE | ID: mdl-6130128

ABSTRACT

Verapamil at 200 microM, prevented the respiratory stimulation, K+ loss, transmitter release, and 45Ca2+ entry into incubated synaptosomes evoked by veratrine (25 to 75 microM) or by high K+ (56 mM). Verapamil (100 microM) also blocked gamma-aminobutyric acid homoexchange, whilst tetrodotoxin was ineffective. Much lower concentrations of verapamil (less than 1 microM) blocked the 45Ca2+ entry caused by veratrine, but not its action in releasing neurotransmitter or K+. It is concluded that verapamil, at 30 to 200 microM, blocks active Na+ channels, thereby preventing depolarization. At greater than 1 microM, verapamil blocks Ca+ channels selectively.


Subject(s)
Amino Acids/metabolism , Cerebral Cortex/metabolism , Neurotransmitter Agents/metabolism , Synaptosomes/metabolism , Verapamil/pharmacology , Animals , Aspartic Acid/metabolism , Biological Transport, Active , Calcium/metabolism , Cerebral Cortex/drug effects , Female , Glutamates/metabolism , Glutamic Acid , Rats , Rats, Inbred Strains , Synaptosomes/drug effects , Tetrodotoxin/pharmacology , Threonine/metabolism , Veratridine/pharmacology , gamma-Aminobutyric Acid/metabolism
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