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  • 1
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Biochemical and Biophysical Research Communications 152 (1988), S. 1185-1192 
    ISSN: 0006-291X
    Keywords: [abr] Alpha 39; the alpha subunits of Go ; [abr] Gi; the identified regulatory components of adenylate cyclase ; [abr] Go; the major G protein from membranes of bovine brain ; [abr] Gs; the identified regulatory components of adenylate cyclase ; [abr] IEF; isoelectrofocusing ; [abr] PT; pertussis toxin ; [abr] SDS-PAGE; sodium dodecyl sulfate polyacrylamide gel ; [abr] alpha 40; the alpha subunits of Gi-like ; [abr] alpha 41; the alpha subunits of proteins
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Biochemical and Biophysical Research Communications 152 (1988), S. 1185-1192 
    ISSN: 0006-291X
    Keywords: [abr] Alpha 39; the alpha subunits of Go ; [abr] Gi; the identified regulatory components of adenylate cyclase ; [abr] Go; the major G protein from membranes of bovine brain ; [abr] Gs; the identified regulatory components of adenylate cyclase ; [abr] IEF; isoelectrofocusing ; [abr] PT; pertussis toxin ; [abr] SDS-PAGE; sodium dodecyl sulfate polyacrylamide gel ; [abr] alpha 40; the alpha subunits of Gi-like ; [abr] alpha 41; the alpha subunits of proteins
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 3
    ISSN: 1432-2013
    Keywords: Key words cAMP ; Neurons ; Patch-clamp ; Potassium channels
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract  Previously, we have described prolonged cAMP-induced inhibition of a K+ current in cultured colliculi neurons. The aim of the present study was to characterize the channel responsible for this cAMP-dependent effect. We detected the presence of a non-inactivating voltage-dependent 16-pS K+ channel that displayed long-lasting inhibition upon a brief application of cAMP and greater sensitivity to tetraethylammonium than to 4-aminopyridine. In addition to this channel, colliculi neurons express two other voltage-sensitive, non-inactivating K+ channels (8 and 49 pS) whose activity is facilitated by a brief application of cAMP, the effect of which is also long-lasting. These results suggest the presence of common sustained cAMP-dependent processes responsible for both up- and down-regulation of these channels in the neurons studied. They indicate that the 16-pS, but not the 8-pS or the 49-pS channels, participates in the cAMP-inhibited macroscopic K+ current.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1432-2013
    Keywords: Cerebellum ; Potassium channels ; Dihydropyridines ; Mouse
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract In cultured cerebellar granule cells, we examined the effects of dihydropyridines (DHPs) on K+ currents, using the whole-cell recording configuration of the patch-clamp technique and on Ca2+-activated K+ channels (“maxi K+ channels”) using outside-out patches. We found that micromolar concentrations of nicardipine, nifedipine, (+) and (−) BAY K 8644, nitrendipine, nisoldipine and (−) nimodipine block 10–60% of macroscopic K+ currents. The most potent of these DHPs was nicardipine and the least potent, (−) BAY K 8644. (+) Nimodipine had no effect on this current. The inhibitory effects of nifedipine and nicardipine were not additive with those of 1 mM tetraethylammonium (TEA). Outside-out recordings of “maxi K+ channels” showed a main conductance of 200 pS (in 77% of the patches) and two subconductance states (in 23% of the patches). Neither nifedipine nor nicardipine affected the main conductance, but decreased the values of the subconductance levels. In 10% of these patches, nicardipine induced a flickering activity of the channel. These findings show that both Ca2+ and K+ channels have DHP-sensitive sites, suggesting similarity in electrostatic binding properties of these channels. Furthermore, cerebellar granule cells may express different subtypes of “maxi K+ channels” having different sensitivities to DHPs. These drugs may provide new tools for the molecular study of K+ channels.
    Type of Medium: Electronic Resource
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