Journal
JOURNAL OF NEUROSCIENCE
Volume 25, Issue 2, Pages 454-463Publisher
SOC NEUROSCIENCE
DOI: 10.1523/JNEUROSCI.3045-04.2005
Keywords
climbing fiber; deep cerebellar nuclei; floccular target neurons; Na channel; internode; action potential burst
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Funding
- NINDS NIH HHS [NS047991, F31 NS047991, R37 NS039395, NS39395, R01 NS039395, R56 NS039395] Funding Source: Medline
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In cerebellar Purkinje neurons, the reliability of propagation of high-frequency simple spikes and spikelets of complex spikes is likely to regulate inhibition of Purkinje target neurons. To test the extent to which a one-to-one correspondence exists between somatic and axonal spikes, we made dual somatic and axonal recordings from Purkinje neurons in mouse cerebellar slices. Somatic action potentials were recorded with a whole-cell pipette, and the corresponding axonal signals were recorded extracellularly with a loose-patch pipette. Propagation of spontaneous and evoked simple spikes was highly reliable. At somatic firing rates of similar to200 spikes/sec, <10% of spikes failed to propagate, with failures becoming more frequent only at maximal somatic firing rates (similar to 260 spikes/sec). Complex spikes were elicited by climbing fiber stimulation, and their somatic waveforms were modulated by tonic current injection, as well as by paired stimulation to depress the underlying EPSCs. Across conditions, the mean number of propagating action potentials remained just above two spikes per climbing fiber stimulation, but the instantaneous frequency of the propagating spikes changed, from similar to 375 Hz during somatic hyperpolarizations that silenced spontaneous firing to similar to 150 Hz during spontaneous activity. The probability of propagation of individual spikelets could be described quantitatively as a saturating function of spikelet amplitude, rate of rise, or preceding interspike interval. The results suggest that ion channels of Purkinje axons are adapted to produce extremely short refractory periods and that brief bursts of forward-propagating action potentials generated by complex spikes may contribute transiently to inhibition of postsynaptic neurons.
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