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The Journal of Neurophysiology Vol. 84 No. 4 October 2000, pp. 1814-1825
Copyright ©2000 by the American Physiological Society
1Neuroscience Program and 2Department of Cell and Molecular Biology, Tulane University, New Orleans, Louisiana 70118
Luther, Jason A.,
Katalin
Cs. Halmos, and
Jeffrey G. Tasker.
A Slow Transient Potassium Current Expressed in a Subset of
Neurosecretory Neurons of the Hypothalamic Paraventricular Nucleus. J. Neurophysiol. 84: 1814-1825, 2000. Type I putative magnocellular neurosecretory cells of the
hypothalamic paraventricular nucleus (PVN) express a prominent
transient outward rectification generated by an A-type potassium
current. Described here is a slow transient outward current that alters cell excitability and firing frequency in a subset of type I PVN neurons (38%). Unlike most of the type I neurons (62%), the transient outward current in these cells was composed of two kinetically separable current components, a fast activating, fast inactivating component, resembling an A-type potassium current, and a slowly activating [10-90% rise time: 20.4 ± 12.8 (SE) ms],
slowly inactivating component (time constant of inactivation:
= 239.0 ± 66.1 ms). The voltage dependence of activation and
inactivation and the sensitivity to block by 4-aminopyridine (5 mM) and
tetraethylammonium chloride (10 mM) of the fast and slow components
were similar. Compared to the other type I neurons, the neurons that
expressed the slow transient outward current were less excitable when
hyperpolarized, requiring larger current injections to elicit an action
potential (58.5 ± 13.2 vs. 15.4 ± 2.4 pA; 250-ms duration;
P < 0.01), displaying a longer delay to the first
spike (184.9 ± 15.7 vs. 89.7 ± 8.8 ms with 250- to
1,000-ms, 50-pA current pulses; P < 0.01), and firing
at a lower frequency (18.7 ± 4.6 vs. 37.0 ± 5.5 Hz with 100-pA current injections; P < 0.05). These data
suggest that a distinct subset of type I PVN neurons express a novel
slow transient outward current that leads to a lower excitability.
Based on double labeling following retrograde transport of systemically
administered fluoro-gold and intracellular injection of biocytin, these
cells are neurosecretory and are similar morphologically to
magnocellular neurosecretory cells, although it remains to be
determined whether they are magnocellular neurons.
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