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  • 1
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] Intracellular patch-clamp recordings were performed in acutely isolated dorsal root ganglion cells from 10-13-day-old chick embryos13'14. Figure la shows the change in action potential waveform induced by OAG15 (5 jxm), which was delivered by pressure application through a micropipette ...
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-2013
    Keywords: Key words AMPA receptor-mediated EPSCs ; Cyclothiazide ; Hippocampus ; Kinetics ; Long-term potentiation (LTP) ; Rat
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract  We have analysed whether the expression of long-term potentiation (LTP) in rat hippocampal CA1 neurons involves a change in the kinetics of (S)-α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptor-mediated excitatory postsynaptic currents (EPSCs) (AMPA-EPSCs) or their susceptibility to the AMPA receptor modulator cyclothiazide. AMPA-EPSCs in the CA1 region were evoked by alternate stimulation of two independent Schaffer collateral-commissural inputs of slices of adult rat hippocampus. In the current-clamp mode a strong tetanus (100 Hz, 1 s) applied to one input (input I) induced stable LTP of AMPA-EPSCs in this input, while the control input (input II) remained unaffected. For neither input were EPSC rise time and decay kinetics significantly changed. The application of cyclothiazide prolonged the rise time and the decay time constants of the AMPA-EPSCs in both control and potentiated inputs to the same extent (Input I–rise time: 198±8%, decay: 148±12%; input II–rise time: 212±14%, decay: 144±19%; n=8). Furthermore, when present during tetanization cyclothiazide did not occlude LTP, suggesting that cyclothiazide and tetanic stimulation enhance AMPA-EPSCs via independent mechanisms. Our findings argue against changes in (de-)activation or desensitization of AMPA receptors as the molecular basis for the expression of LTP.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Pflügers Archiv 425 (1993), S. 499-505 
    ISSN: 1432-2013
    Keywords: Helix bursting neurons ; Calcium imaging ; Calcium buffering
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Bursting pacemaker neurons of the snail Helix pomatia were voltage-clamped and Ca currents in response to depolarizing steps were recorded. Simultaneously, changes in intracellular Ca concentrations were measured using the fluorescent dye fura-2 and a highly sensitive digital camera. Ca influx through voltage-gated channels induced a spatially non-uniform increase in intracellular Ca. The Ca signals decayed with a time constant of about 5 s. By increasing the concentration of the indicator dye, its Ca-buffering capacity was enhanced and Ca transients in response to depolarization were diminished. Thereby, the endogenous Ca buffer capacity could be determined and was calculated to be about 480 buffered ions for every free Ca ion. The buffer capacity did not vary significantly with the amount of Ca influx within the range tested, suggesting that the buffer is not saturated at Ca concentrations of up to 1μM.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Cellular and molecular neurobiology 7 (1987), S. 229-236 
    ISSN: 1573-6830
    Keywords: second messengers ; channel gating ; patch clamp ; cyclic AMP ; cyclic GMP ; calcium ions
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary 1. There is widespread belief that intracellular messengers [e.g., Ca2+, cyclic AMP, cyclic GMP, inositol-1,4,5-triphosphate (IP3)] assert their actions primarily through activation of protein kinases. 2. In studies of excitable cells protein kinase activation has been shown to alter membrane ionic conductance, presumably through phosphorylation of ion channels (see Levitan, 1985). However, recent reports from several laboratories indicate that intracellular messengers can also affect membrane ionic conductances directly without invoking protein kinase activation. 3. In this article we examine those examples of direct activation of ionic conductances by intracellular messengers which are supported by single-channel studies of isolated membrane patches. The list of cell types displaying this kind of response is growing and includes cells of neuronal as well as nonneuronal origin.
    Type of Medium: Electronic Resource
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