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  • 1
    ISSN: 1432-1106
    Keywords: Synaptic-Plasticity ; Cerebellum ; Metabotropic-glutamate-receptor ; Rat
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Using an in vitro slice preparation, we studied the effects, on parallel fiber (PF)-mediated EPSPs, of coactivation of metabotropic-glutamate receptors and of voltage-gated calcium (Ca) channels of Purkinje cells (PCs) by bath application of 50 μM trans-1-aminocyclopentyl-1,3-dicarboxylate (trans-ACPD) and by direct depolarization of the cells, respectively. These effects were compared with changes in synaptic efficacy obtained when α-amino-3hydroxy-5-methylisoxalone-4-propionate (AMPA) receptors of PCs were also activated through stimulation of PFs during the pairing protocol, as well as when similar experiments were performed without trans-ACPD in the bath. In a control medium, pairing for 1 min of PF-mediated EPSPs evoked at 1 Hz with Ca spikes evoked by steady depolarization of PCs (n = 13) led to LTD of synaptic transmission in 9 cases whereas for the others EPSPs were not affected. No LTD occurred in 9 out of 10 other cells tested when PF stimulation was omitted during the 1 min period of Ca spike firing of PCs. Bath application of 50 μM trans-ACPD, in conjunction with the same pairing protocol as before (n = 8), led to a significantly larger LTD of PF-mediated EPSPs after washing out of this drug. Moreover, a clearcut LTD of PF-mediated EPSPs was also observed in 5 of the 8 other cells, when PF stimulation was omitted during Ca spike firing in the presence of trans-ACPD. As trans-ACPD alone induced fully reversible depressions of EPSPs, coactivation of metabotropic-glutamate receptors and of voltage-gated Ca channels is therefore likely to be sufficient to induce LTD of PF-mediated EPSPs.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Experimental brain research 107 (1995), S. 197-204 
    ISSN: 1432-1106
    Keywords: Slowly inactivating potassium currents ; Patch-clamp ; Cortical neurons ; Rat
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Slowly inactivating outward currents were examined in neurons from rat anterior cortex dissociated at postnatal day 1 and recorded after 7–48 days in vitro by the use of whole-cell patch-clamp technique, in the presence of 0.5–0.8 μM tetrodotoxin (TTX), 50 μM carbachol and 1–5 mM CsCl2. Experiments were often carried out in the additional presence of 1–5 mM CsCl2, which blocks the anomalous, inwardly rectifying I Q, the fast Ca 2 + -dependent K+ current (I C), and 50 μM carbachol, which depresses the I M current. These currents were evoked by depolarizing steps to -40+-5 mV from a conditioning hyperpolarization to -110+-10 mV. Their sensitivity to elevation from 2.5 to 12.5 mM in extracellular K+ concentration, together with their sensitivity to 5–15 mM tetraethylammonium, suggests that they are mainly carried by K+ ions. Their activation and inactivation curves show that the threshold for activation is -65 mV, that their inactivation is achieved at -75 mV and that potentials more negative than -120 mV are needed to abolish it. The time-dependence of de-inactivation gives a maximal current amplitude for conditioning hyperpolarizations of 2 s and is best described by a monoexponential function with a time constant of 0.7 s. Slow, transient K+ currents were depressed by low doses of 4-aminopyridine (30–100 μM), which indicates the occurrence of an I D-type component in the recorded K+ currents. No slowly declining K+ current was expressed when a recording solution containing 10 mM 1,2-bis(2-aminophenoxy)ethane-N, N,N′-N′-tetraacetic acid (BAPTA), instead of 1–5 mM BAPTA, was used. When recorded without Ca2+ chelator in the pipette, slowly declining K+ currents were blocked by bath-applied 40–50 μM BAPTA-aminoethoxy, revealing a large-amplitude, rapidly inactivating outward current. This residual component is insensitive to 50 μM 4-aminopyridine and may include a current more related to the I A-type. Our data provide evidence that, in cultured cortical neurons from rat, the expression of an I D-like K+ current is highly dependent on internal Ca2+ concentration.
    Type of Medium: Electronic Resource
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