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J Neurochem ; 40(2): 514-21, 1983 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-6130128

RESUMO

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.


Assuntos
Aminoácidos/metabolismo , Córtex Cerebral/metabolismo , Neurotransmissores/metabolismo , Sinaptossomos/metabolismo , Verapamil/farmacologia , Animais , Ácido Aspártico/metabolismo , Transporte Biológico Ativo , Cálcio/metabolismo , Córtex Cerebral/efeitos dos fármacos , Feminino , Glutamatos/metabolismo , Ácido Glutâmico , Ratos , Ratos Endogâmicos , Sinaptossomos/efeitos dos fármacos , Tetrodotoxina/farmacologia , Treonina/metabolismo , Veratridina/farmacologia , Ácido gama-Aminobutírico/metabolismo
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