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The Journal of Neurophysiology Vol. 83 No. 2 February 2000, pp. 971-983
Copyright ©2000 by the American Physiological Society
1Howard Hughes Medical Institute, Computational Neurobiology Laboratory, The Salk Institute, La Jolla 92037; and 2Department of Physics, 3Neurobiology Unit, Scripps Institution of Oceanography, 4Department of Neuroscience, and 5Department of Biology, University of California, San Diego, La Jolla, California 92093
Moortgat, Katherine T.,
Theodore H. Bullock, and
Terrence J. Sejnowski.
Precision of the Pacemaker Nucleus in a Weakly Electric Fish:
Network Versus Cellular Influences. J. Neurophysiol. 83: 971-983, 2000. We investigated the relative
influence of cellular and network properties on the extreme spike
timing precision observed in the medullary pacemaker nucleus (Pn) of
the weakly electric fish Apteronotus leptorhynchus. Of
all known biological rhythms, the electric organ discharge of this and
related species is the most temporally precise, with a coefficient of
variation (CV = standard deviation/mean period) of 2 × 10
4 and standard deviation (SD) of 0.12-1.0 µs. The
timing of the electric organ discharge is commanded by neurons of the
Pn, individual cells of which we show in an in vitro preparation to
have only a slightly lesser degree of precision. Among the 100-150 Pn
neurons, dye injection into a pacemaker cell resulted in dye coupling
in one to five other pacemaker cells and one to three relay cells, consistent with previous results. Relay cell fills, however, showed profuse dendrites and contacts never seen before: relay cell dendrites dye-coupled to one to seven pacemaker and one to seven relay cells. Moderate (0.1-10 nA) intracellular current injection had no effect on
a neuron's spiking period, and only slightly modulated its spike
amplitude, but could reset the spike phase. In contrast, massive
hyperpolarizing current injections (15-25 nA) could force the cell to
skip spikes. The relative timing of subthreshold and full spikes
suggested that at least some pacemaker cells are likely to be intrinsic
oscillators. The relative amplitudes of the subthreshold and full
spikes gave a lower bound to the gap junctional coupling coefficient of
0.01-0.08. Three drugs, called gap junction blockers for their mode of
action in other preparations, caused immediate and substantial
reduction in frequency, altered the phase lag between pairs of neurons,
and later caused the spike amplitude to drop, without altering the
spike timing precision. Thus we conclude that the high precision of the
normal Pn rhythm does not require maximal gap junction conductances
between neurons that have ordinary cellular precision. Rather, the
spiking precision can be explained as an intrinsic cellular property
while the gap junctions act to frequency- and phase-lock the network oscillations.
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