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J Neurophysiol (November 1, 2002). 10.1152/jn.00057.2002
Submitted on 29 January 2002
Accepted on 11 June 2002
1Department of Neurobiology, School of Medicine and 2Department of Computer Science, Yale University, New Haven, Connecticut 06520-8001; 3College of Life Science, Zhejiang University, Hangzhou, Zhejiang 310027, China; and 4Department of Medical Physiology, University of Copenhagen, 7400 Copenhagen, Denmark
Chen, Wei R.,
Gongyu Y. Shen,
Gordon M. Shepherd,
Michael L. Hines, and
Jens Midtgaard.
Multiple Modes of Action Potential Initiation and Propagation in
Mitral Cell Primary Dendrite. J. Neurophysiol. 88: 2755-2764, 2002. The mitral cell primary dendrite plays
an important role in transmitting distal olfactory nerve input from
olfactory glomerulus to the soma-axon initial segment. To understand
how dendritic active properties are involved in this transmission, we
have combined dual soma and dendritic patch recordings with
computational modeling to analyze action-potential initiation and
propagation in the primary dendrite. In response to depolarizing
current injection or distal olfactory nerve input, fast
Na+ action potentials were recorded along the
entire length of the primary dendritic trunk. With weak-to-moderate
olfactory nerve input, an action potential was initiated near the soma
and then back-propagated into the primary dendrite. As olfactory nerve input increased, the initiation site suddenly shifted to the distal primary dendrite. Multi-compartmental modeling indicated that this
abrupt shift of the spike-initiation site reflected an independent thresholding mechanism in the distal dendrite. When strong olfactory nerve excitation was paired with strong inhibition to the mitral cell
basal secondary dendrites, a small fast prepotential was recorded at
the soma, which indicated that an action potential was initiated in the
distal primary dendrite but failed to propagate to the soma. As the
inhibition became weaker, a "double-spike" was often observed at
the dendritic recording site, corresponding to a single action
potential at the soma. Simulation demonstrated that, in the course of
forward propagation of the first dendritic spike, the action potential
suddenly jumps from the middle of the dendrite to the axonal
spike-initiation site, leaving the proximal part of primary dendrite
unexcited by this initial dendritic spike. As Na+
conductances in the proximal dendrite are not activated, they become
available to support the back-propagation of the evoked somatic action
potential to produce the second dendritic spike. In summary, the
balance of spatially distributed excitatory and inhibitory inputs can
dynamically switch the mitral cell firing among four different modes:
axo-somatic initiation with back-propagation, dendritic initiation
either with no forward propagation, forward propagation alone, or
forward propagation followed by back-propagation.
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