Based on these observations, the first node either indirectly facilitates high-frequency bursts by generating an inward current at subthreshold potentials or directly initiates APs within a burst. APs during a high-frequency burst are known

to be generated in the axon, but the role of the first node has not been precisely determined (Williams and Stuart, 1999). Rare cases of initiation of APs in the first node have been reported in Purkinje axons (Palmer et al., 2010). To distinguish between the AIS and the node as possible initiation sites, axosomatic delays during high-frequency bursts were determined by making extracellular action potential (eAP) recordings simultaneously from both locations in combination with whole-cell Selleck Target Selective Inhibitor Library somatic recording (Figure 5A). Using fluorescence-guided axon visualization, patch-pipettes filled with extracellular

solution were placed check details near the end of the AIS (on average 40 ± 3 μm) and at the first node of the same axon (162 ± 34 μm distance from the soma). AP bursts were triggered with somatic suprathreshold current injections in IB neurons (98–211 Hz, n = 5). APs within a burst were separately averaged (40–80 trials) by alignment to the onset of the somatic AP (first peak in the d2V/dt2, Figure 5B). The results show that for the first spike in a burst, the eAP onset latency in the AIS was on average −74 ± 9.8 μs (range from −38 to −93 μs, n = 5) and preceding the eAP at the first node (+14 ±

10 μs, p < 0.01, n = 5, Figures 5B and 5C). For each paired recording, the AIS-to-node latency was negative (range from −30 to −110 μs, average −87 ± 16 μs, n = 5), indicating that the first AP within a high-frequency burst is starting in the AIS. This spatiotemporal sequence was almost identical for the second AP in the burst (AIS-to-node latency, −136 ± 20 μs, n = 5, p < 0.01, Figures 5B and 5C). Furthermore, in one case of an AP burst with three spikes, the third AP also had a negative AIS-to-node latency (−148 μs), suggesting spike initiation is robust in the AIS. Based on the distances between recording sites, the AIS-to-soma antidromic conduction velocity was estimated to be 0.67 ± 0.10 m s−1 and 1.48 ± 0.37 m s−1 for the orthodromic propagation through the first internode (n = 5). Thus, all APs Mannose-binding protein-associated serine protease during high-frequency firing are initiated in the AIS, and the importance of the first branchpoint is likely to be indirect (e.g., through a conductance active in the subthreshold voltage range). Voltage-gated Na+ channels are known to produce three types of currents, operationally defined by their distinct kinetics: a large and fast-inactivating Na+ current underlying the AP upstroke (INaT), a transient resurgent current activated during repolarization (INaR), and a noninactivating persistent current active in the subthreshold range (INaP). Since nodes of Ranvier contain a high density of Na+ channels ( Caldwell et al.