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The Journal of Neurophysiology Vol. 84 No. 6 December 2000, pp. 2896-2903
Copyright ©2000 by the American Physiological Society
Department of Molecular and Integrative Physiology and Neuroscience Program, University of Illinois at Urbana-Champaign, Urbana, Illinois 61801
Fan, Yi-Ping,
Eric M. Horn, and
Tony G. Waldrop.
Biophysical Characterization of Rat Caudal Hypothalamic Neurons:
Calcium Channel Contribution to Excitability. J. Neurophysiol. 84: 2896-2903, 2000. Neurons in the
caudal hypothalamus (CH) are responsible for the modulation of various
processes including respiratory and cardiovascular output. Previous
results from this and other laboratories have demonstrated in vivo that
these neurons have firing rhythms matched to the respiratory and
cardiovascular cycles. The goal of the present study was to
characterize the biophysical properties of neurons in the CH with
particular emphasis in those properties responsible for rhythmic firing
behavior. Whole cell, patch-clamped CH neurons displayed a resting
membrane potential of
58.0 ± 1.1 mV and an input resistance of
319.3 ± 16.6 M
when recorded in current-clamp mode in an in
vitro brain slice preparation. A large proportion of these neurons
displayed postinhibitory rebound (PIR) that was dependent on the
duration and magnitude of hyperpolarizing current as well as the
resting membrane potential of the cell. Furthermore these neurons
discharged tonically in response to a depolarizing current pulse at a
depolarized resting membrane potential (more positive than
65 mV) but
switched to a rapid burst of firing to the same stimulus when the
resting membrane potential was lowered. The PIR observed in these
neurons was calcium dependent as demonstrated by the ability to block
its amplitude by perfusion of Ca2+-free bath
solution or by application of Ni2+ (0.3-0.5 mM)
or nifedipine (10 µM). These properties suggest that
low-voltage-activated (LVA) calcium current is involved in the PIR and
bursting firing of these CH neurons. In addition, high-voltage-activated calcium responses were detected after blockade of outward potassium current or in
Ba2+-replacement solution. In addition, almost
all of the CH neurons studied showed spike frequency adaptation that
was decreased following Ca2+ removal, indicating
the involvement of Ca2+-dependent
K+ current
(IK,Ca) in these cells. In conclusion,
CH neurons have at least two different types of calcium currents that
contribute to their excitability; the dominant current is the LVA or
T-type. This LVA current appears to play a significant role in the
bursting characteristics that may underlie the rhythmic firing of CH neurons.
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