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J Neurophysiol (December 1, 2002). 10.1152/jn.00350.2002
Submitted on 8 May 2002
Accepted on 8 August 2002
1Department of Neurology and 2Department of Pediatrics, Yale University School of Medicine, New Haven Connecticut 06510
Cummins, Theodore R.,
Sulayman D. Dib-Hajj,
Stephen G. Waxman, and
David F. Donnelly.
Characterization and Developmental Changes of Na+
Currents of Petrosal Neurons With Projections to the Carotid Body. J. Neurophysiol. 88: 2993-3002, 2002. Carotid body
chemoreceptors transduce a decrease in arterial oxygen tension into an
increase in spiking activity on the sinus nerve, and this response
increases with postnatal age over the first week or two of life.
Previous work from our laboratory has suggested a major role of axonal
Na+ channels in the initiation of afferent
spiking activity. Using RT-PCR of the petrosal ganglia we identified
Na+ channel TTX-S isoforms
Nav1.1, Nav1.6, and
Nav1.7 and the TTX-resistant (TTX-R) isoforms
Nav1.8 and Nav1.9 at high
levels. Electrophysiologic recordings (at 3 ages: 3 days, 9 days,
18-20 days) of neurons that project to the carotid body exhibited
predominantly fast-inactivating sodium currents, with a bimodal
recovery from inactivation at
80 mV (fast component ~ 8 ms;
slow component ~90 ms). Developmental age had little effect with no
change in peak current density (approximately 1.4 nA/pF) and was
associated with a slight, but significant increase in the speed of
recovery from inactivation at
140 and
120 mV but not at other
potentials. Assuming that the same Na+ channel
complement is present at the nerve terminal as at the soma, the
association of a sensory modality (chemoreception) with a relatively
uniform Na+ channel profile suggests that the
rapid kinetics of TTX-S channels may be essential for some aspects of
chemoreceptor function beyond mediating simple axonal conduction.
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