Stoichiometry of the Heteromeric Nicotinic Receptors of the Renshaw Cell

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Figure 6.
Figure 6.

Effects of Zn (10 and 100 μm) on the sEPSCs and the eEPSCs. A1, Effects of Zn (10 and 100 μm) on eEPSCs (10 traces). CTL: a1 −308 pA, a2 −25.4 pA, τ1 10.6 ms, τ2 81.3 ms, τw 16.0 ms. Zn 10 μm: a1 −293 pA, a2 −25.9 pA, τ1 11.4 ms, τ2 78.4 ms, τw 16.8 ms. Zn 100 μm: a1 −134 pA, a2 −21.3 pA, τ1 12.6 ms, τ2 87.7 ms, τw 22.9 ms. A2, Effects of Zn (100 μm) on the sEPSCs (inset) (same experiment as in A1). The records illustrated correspond to sEPSCs recorded on a 150 ms time base and fit with a single exponential (control: 194 events, −12 pA, td 8.8 ms; Zn 10 μm: 356 events, −14.5 pA, td 9.1 ms; Zn 100 μm: 592 events −13 pA, td = 12.8 ms). The values of the kinetic parameters for a dual exponential fit were also measured on a 540 ms time base, but this reduced the number of events. B1, Effects of Zn (100 μm) on eEPSCs. There was no significant change in the two time constants of the decay. The reduction of the amplitude was more important for a1 than for a2. B2, Effects on eEPSCs of reducing the external Ca concentration from 2 to 1 mm. There was no significant change in the two time constants of the decay. The reduction of the amplitude was slightly higher for a1 than for a2, leading to a slight increase in the ratio a2/a1 (p = 0.016; n = 7). C, Ratio of the two amplitudes a1 and a2 in presence of Zn (100 μm) and in reduced Ca (1 mm). The ratio is increased by Zn from 0.14 ± 0.06 to 0.61 ± 0.41 (n = 7; p = 0.01; C1) and unchanged (control 0.27 ± 0.12; reduced Ca 0.15 ± 0.03; n = 7; p = 0.07 bilateral paired t test) when the release is reduced presynaptically by lowering the Ca concentration (C2).

  1. The Journal of Neuroscience vol. 38 no. 21 4943-4956
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