Our voltage-clamp experiments demonstrate that both N- and T-type currents can induce SK channel opening, both when short (2 ms) and long (20 ms) depolarizing voltage steps are produced. L-, R- and P/Q channels are not effective in this respect. These results are consistent with those of Penington & Fox (1995), who did not observe any P-, Q-, or R-Type Ca2+ currents in raphe neurons. It is intriguing that co-application of mibefradil and ω-conotoxin did not inhibit the outward current more than either agent alone after long pulses (see below).

In addition, the combination of the two blockers did not abolish the current in voltage-clamp experiments, suggesting that another, minor, source of Ca2+ could exist in these neurons. However, the percentage block after short pulses amounted to ~90% and the AZD6244 small size of this residual current precluded a thorough analysis of its properties. In current clamp, we only found evidence of a role for N-type channels in

the generation of the mAHP, in apparent contradiction to the voltage-clamp data. However, it should be remembered that voltage-clamp data were obtained in the presence of 5 mm TEA. The use of this compound was needed to block other K+ currents which would otherwise have contaminated our measurements. It is probable that this compound altered the membrane potential waveform in the dendrites as well as the extent of the dendritic compartment that followed the voltage command. Therefore, one reasonable explanation of this discrepancy is that more remote areas learn more of the dendrites were exposed to more depolarized voltages during our voltage-clamp steps than during natural action potentials. This would imply that N-type channels are more proximal to the soma and T-type channels more distal.

There is evidence for this in other neurons. For example, T-type channels are clearly located in distal dendrites of thalamic reticular nucleus neurons (Crandall et al., 2010). It is not possible from our data to infer what the location of SK channels is within serotonergic neurons. However, studies in other types of neurons have suggested that these channels are located both on the soma and on the dendrites, where they may play (-)-p-Bromotetramisole Oxalate different roles. This seems to be the case both in hippocampal pyramidal (Adelman et al., 2012) and in dopaminergic (Deignan et al., 2012) neurons. In the first case, dendritic SK channels are involved in a local negative feedback loop where they inhibit Ca2+ influx through NMDA channels by their hyperpolarizing effect (Ngo-Anh et al., 2005). In this regard, one possible explanation for the lack of additive effect of mibefradil and ω-conotoxin in voltage clamp is that both N- and T-type channels may activate the same population of SK channels in serotonergic neurons. Further experiments are, however, needed to test this hypothesis, as well as to decipher the topography of SK channels and voltage-dependent Ca2+ channels in these neurons.