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. 2017 Jun 5;13(6):e1005565. doi: 10.1371/journal.pcbi.1005565

Fig 7. The effect of the lower voltage bound Vlow of oscillations on fres and Zmax constrains the optimal models.

Fig 7

a. An example of the change in Z(f) measured in the biological PD neuron for Vlow = -60mV (black line) and Vlow = -70mV (grey line). Inset shows the bounds of voltage clamp inputs in the two cases. b. Shifting Vlow from -60 mV to -70 mV lowers the value of fres measured in the PD neuron significantly, without influencing Zmax (b. Experimental). fres and Zmax values measured in a random subset of optimal model neurons corresponding to low or high g¯Ca values produced the same fres and Zmax values at Vlow = -60mV (black dots), but distinct fres and Zmax values at Vlow = -70mV (low g¯Ca: red dots; high g¯Ca: cyan dots). A subset of optimal models could reproduce the experimental result in which fres shifted to significantly lower values without affecting Zmax. (grey dots). (c) g¯CaV1/2Cah relationship separating out the different groups of models producing different responses to changes in Vlow (colors correspond to b Model panel). Models depicted by grey dots are referred to as intermediate g¯Ca models. (d1-e3) mean voltage-gated ionic currents ICa, IH and ICa+IH and Itotal, shown as a function of voltage for Vlow = -60 mV (d1-d3) and Vlow = -70 mV (e1-e3). Numbers correspond to the location along the g¯CaV1/2Cah as shown in c. f. The intermediate g¯Ca models (grey dots) show a distinct g¯CaV1/2Cah linear correlation. g. Intermediate g¯Ca models (grey dots) show a distinct and tighter τmCaτhCa correlation compared to all optimal models (black dots). h. Intermediate g¯Ca models (grey dots) show a strong g¯Cag¯H linear correlation that is not observed for all optimal models (black dots).