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Electrophysiological properties of the tongue epithelium of the toad Bufo marinus

Timothy K. Baker, Karina Rios and Stanley D. Hillyard*

Department of Biological Sciences, University of Nevada Las Vegas, Las Vegas, NV 89154-4004, USA



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Fig. 1. A recording from a typical experiment in which NaCl and KCl Ringer were exchanged sequentially as the mucosal and serosal bathing solutions. The solution changes (mucosal/serosal) are indicated on the figure. Isc, short-circuit current.

 


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Fig. 2. Power spectra obtained from experiments with (A) NaCl Ringer as the mucosal and serosal bathing solutions, (B) NaCl Ringer as the serosal solution and KCl Ringer as the mucosal solution and (C) NaCl Ringer as the mucosal solution and KCl Ringer as the serosal solution. Note the presence of two Lorentzian components in C. The spectra from A and B are from sequential treatments of the same preparation as depicted in Fig. 1. Sf, spectral density. The arrows on the spectra indicate the range of data points selected for the computer fit of the spectra using equation 1.

 


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Fig. 3. The inhibition of short-circuit current (Isc) by the addition of Ba2+ to the mucosal Ringer's solution. The x axis scale reflects the sequence of treatments, which were applied at approximately regular intervals. In these experiments, the mucosal and serosal baths were NaCl Ringer. Isc values marked with an asterisk are significantly inhibited relative to the control value. Removal of Ba2+ restores Isc to its control value. The changes in the power density of the Lorentzian plateau at low frequencies (So) and the corner frequency (fc) are not significant. Values are means ± S.E.M., N=6.

 


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Fig. 4. Direct linear plots for Ba2+ inhibition of short-circuit current (Isc). (A) Experiments with NaCl as the mucosal and serosal bathing solution; the mean control value of Isc was -13.00 µA cm-2 (the y intercepts are the means for six experiments). (B) Experiments with NaCl and KCl as the mucosal and serosal solutions, respectively (N=4). The mean control Isc for these experiments was -30.37 µA cm-2. Note that the lines do not all intersect at a common point as would be predicted if the Ba2+ inhibition were due to binding to a single site with a single binding affinity. The broken lines indicate the x intercept in A and B, which is the Ki value for Ba2+ inhibition at lower concentrations. In B, the broken horizontal line indicates the blocker-sensitive Isc (not drawn in A).

 


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Fig. 5. The inhibition of short-circuit current (Isc) by 10 and 100 µmol l-1 quinine added to the mucosal Ringer. Note that removal of quinine does not reverse the inhibition of Isc, while the addition of 10 mmol l-1 Ba2+ does produce a further inhibition that is reversible. In all experiments, NaCl Ringer was the mucosal and serosal bathing solution. The values for the Lorentzian plateau at low frequencies (So) decrease with Isc as the quinine concentration is increased and remain low after quinine wash-out and during Ba2+ treatment. So does increase when Isc values return to more negative values following the removal of Ba2+. Values marked with an asterisk indicate that Isc and So are reduced significantly relative to the control values. The value marked with a dagger indicates that the value of Isc following treatment with 10 mmol l-1 Ba2+ is significantly different from the quinine wash-out value. The corner frequencies (fc) do not change significantly over the course of the mucosal solution changes. Values are means ± S.E.M., N=6.

 





© The Company of Biologists Ltd 2002