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1.
Neuropharmacology ; 39(2): 235-45, 2000 Jan 04.
Artigo em Inglês | MEDLINE | ID: mdl-10670419

RESUMO

Loreclezole had two different effects on GABA(A) receptor (GABAR) currents. When applied to GABARs that contained a beta2 or beta3 subunit subtype, but not a beta1 subtype, loreclezole potentiated the peak current evoked by sub-maximal concentrations of GABA. Loreclezole also increased the rate and degree of apparent desensitization of GABAR whole-cell currents, an effect that was independent of the beta subunit subtype, suggesting that potentiation and inhibition of GABAR current by loreclezole occurred through separate sites. We used patch-clamp recording from outside-out and inside-out patches from L929 fibroblasts transiently transfected with rat GABAR subunits to examine the properties of inhibition of alpha1beta1gamma2L single channel currents by loreclezole. Loreclezole decreased the mean open time of the channel by decreasing the average durations of the open states. Loreclezole also increased the occurrence of a closed component with an average duration near 20 ms. Inhibition by loreclezole was not voltage-dependent. Loreclezole was equally effective when applied to the intracellular side of the receptor, suggesting that its binding site was readily accessible from both sides of the membrane. Pre-application of loreclezole effectively inhibited the GABAR current in macropatches, indicating that binding did not require an open channel. These findings were consistent with a mechanism of allosteric modulation at a site formed by the membrane spanning regions of the receptor.


Assuntos
Antagonistas de Receptores de GABA-A , Triazóis/farmacologia , Animais , Anticonvulsivantes/farmacologia , Encéfalo/fisiologia , Células Cultivadas , Citoplasma/efeitos dos fármacos , Citoplasma/fisiologia , Eletrofisiologia , Moduladores GABAérgicos/farmacologia , Humanos , Cinética , Potenciais da Membrana/efeitos dos fármacos , Camundongos , Técnicas de Patch-Clamp , Isoformas de Proteínas/antagonistas & inibidores , Isoformas de Proteínas/genética , Isoformas de Proteínas/fisiologia , Ratos , Receptores de GABA-A/genética , Receptores de GABA-A/fisiologia , Proteínas Recombinantes
2.
Behav Neurosci ; 108(1): 94-9, 1994 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-8192854

RESUMO

The ciliate protozoa, Stentor and Paramecium, have been reported to escape from the bottom end of narrow capillary tubes into a larger volume of medium with increasing rapidity over the course of trials. This change in behavior has been considered an apparent example of associative learning. This decrease in escape time is not due to a change in the protozoa's environment, their swimming speed, frequency of ciliary reversals, or the proportion of time spent forward or backward swimming. Instead, most of the decrease results from a decrease in the proportion of time spent in upward swimming. However, a similar decrease in upward swimming occurs when the task is altered to require escape from the upper end of the capillary tubes. Because the protozoa exhibit the same change in behavior regardless of the reinforcing stimulus, tube-escape learning is not associative learning.


Assuntos
Aprendizagem por Associação , Cilióforos , Condicionamento Clássico , Reação de Fuga , Animais , Orientação , Tempo de Reação , Retenção Psicológica , Meio Social
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