8 ± 64.1 MΩ in control solution, and 277.8 ± 65.6 MΩ after

washin of 30 μM ZD7288, n = 3). This GSK1210151A mw finding is also consistent with the absence of a hyperpolarizing voltage sag both in somatic and dendritic recordings (Figures S1E and S1F). We calculated the Fourier transforms of the somatic and dendritic voltage traces for current injections to the dendritic (Figure 5C) or the somatic electrode (Figure 5D). The frequency-dependent voltage transfer was estimated by computing the ratio of dendritic to somatic Fourier transforms (Figure 5G, filled lines, red: dendrite to soma, blue: soma to dendrite, dark gray indicates SD, n = 6 and n = 9, respectively, distance >50 μm from the soma). These data confirm a strong frequency-dependence of voltage attenuation, with a significantly stronger attenuation at higher frequencies (Wilcoxon signed-rank test of steady-state attenuation (at 0.5 Hz) versus attenuation at 25 Hz, D → S p = 0.031, S → D p = 0.004). These experiments were repeated at depolarized (Figure 5E) and hyperpolarized (Figure 5F) membrane

potentials (average change in dendritic membrane potential +20.5 ± 3.4 and −15.7 ± 0.9 mV, n = 8 and n = 4, respectively). The frequency-dependent voltage transfer was not significantly altered (Wilcoxon rank tests at 0, 5, and 25 Hz, Figure 5G). The frequency-dependent voltage transfer properties assessed with ZAP functions were well replicated in the computational model with passive dendrites (data not shown). During physiological activity granule cell dendrites receive correlated synaptic input with varying degrees www.selleckchem.com/products/BKM-120.html of synchrony. The frequency-dependent properties of granule cell dendrites described above suggest that voltage transfer of highly synchronous synaptic input may be less efficient than inputs with low synchrony. We therefore injected dendritic compound mock EPSCs mimicking inputs of different synchrony.

Compound EPSCs consisted of 5 individual EPSCs separated by a variable time interval Δt ranging Dipeptidyl peptidase from 0.1 to 100 ms (Figures 6A and 6B, current injections shown in black, examples shown for Δt of 0.1 and 10 ms, respectively; red and blue indicate dendritic and somatic voltage recordings). Both types of stimuli were strongly attenuated, but the relative attenuation of the compound EPSP with a Δt of 10 ms was less pronounced (Figure 6C, traces as in Figures 6A and 6B, but scaled to the same peak value at Δt = 0.1 ms). When the peak voltage attained during compound EPSPs at the dendritic and somatic recording sites was plotted versus Δt, both parameters decline with increasing Δt. However, the somatic EPSP was stable over a larger range of Δt (Figure 6D). This effect was due to an enhanced voltage transfer around a Δt of approximately 10 ms (Figure 6E, n = 12, distance >50 μm from the soma).