Terbium modulation of single γ-aminobutyric acid-activated chloride channels in rat dorsal root ganglion neurons

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Abstract

We have previously reported that lanthanides markedly potentiate the GABA- induced chloride current by acting at a distinct site on the GABA(A) receptor-channel complex (Ma and Narahashi, 1993a,b). These studies have now been extended to the single-channel level and changes in gating kinetics of GABA(A) receptor currents caused by 100 μM terbium (Tb3+) are reported. The GABA-induced currents were recorded from outside-out membrane patches isolated from rat dorsal root ganglion neurons in primary culture at a holding potential of -60 mV. At least two conductance levels were recorded, a main conductance of about 26 pS (70-80% of events) and a subconductance of about 19 pS (20-30 % of events). These two conductances and the ratio of main- and subconductance state currents with respect to the number of events were not changed by Tb3+. The frequency of channel openings was also unchanged in the presence of Tb3+. The frequency histograms of open, close, and burst durations of the main-conductance state were best fitted by a sum of three exponential functions. All of the time constants remained unchanged by application of Tb3+ while the relative proportions of the longest open and burst duration time constants were increased and the relative proportion of longest closed time constant was decreased. We suggest that Tb3+ binds to an allosteric site on the GABA(A) receptor-channel complex to increase the apparent mean open time of the channel by increasing the affinity of GABA for the GABA binding site, and/or by shifting the distribution toward the open states so that the frequency of occurrence of longer open states is stabilized. Tb3+ and other lanthanides will become useful tools to study the structure and function of the GABA receptor-channel complex.

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APA

Ma, J. Y., Reuveny, E., & Narahashi, T. (1994). Terbium modulation of single γ-aminobutyric acid-activated chloride channels in rat dorsal root ganglion neurons. Journal of Neuroscience, 14(6), 3835–3841. https://doi.org/10.1523/jneurosci.14-06-03835.1994

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