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Naunyn Schmiedebergs Arch Pharmacol ; 308(3): 273-9, 1979 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-41193

RESUMO

The influence of adenosine upon the process of transmitter release was investigated in Mg2+-paralyzed frog neuromuscular junction by using conventional microelectrophysiological techniques and binomial statistical analysis. The statistical parameters used were: m (mean number of quanta released per impulse), p (the probability of quantal release) and n (store of quanta available for release). Adenosine decreased the mean quantal content (m) by reducing n. This effect appeared to be dependent upon the free intracellular Ca2+. The nucleoside competed with the transmitter releasing effects of ouabain and increased the amount of effective Ca2+ necessary for quantal release. It did not change the slope of release parameters modification during low-frequency facilitation. The data are discussed in terms of a physical model of release.


Assuntos
Adenosina/farmacologia , Magnésio/farmacologia , Junção Neuromuscular/efeitos dos fármacos , Neurotransmissores/metabolismo , Animais , Anuros , Cálcio/farmacologia , Ouabaína/farmacologia , Ranidae , Fatores de Tempo
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