Precision of the pacemaker nucleus in a weakly electric fish: network versus cellular influences.

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 x 10(-4) and standard deviation (SD) of 0.12-1.0 micros. 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.

[1]  S. Hagiwara,et al.  Analysis of interval fluctuation of the sensory nerve impulse. , 1954, The Japanese journal of physiology.

[2]  G. P. Moore,et al.  Interspike interval fluctuations in aplysia pacemaker neurons. , 1966, Biophysical journal.

[3]  C. Stevens,et al.  Synaptic Noise as a Source of Variability in the Interval between Action Potentials , 1967, Science.

[4]  M. V. Bennett,et al.  Physiology and ultrastructure of electrotonic junctions. IV. Medullary electromotor nuclei in gymnotid fish. , 1967, Journal of neurophysiology.

[5]  K. Abromeit Music Received , 2023, Notes.

[6]  T Szabo,et al.  Effect of temperature on the discharge rates of the electric organ of some gymnotids. , 1968, Comparative biochemistry and physiology.

[7]  T. Bullock The Reliability of Neurons , 1970, The Journal of general physiology.

[8]  Daniel L. Alkon,et al.  Responses of Photoreceptors in Hermissenda , 1972, The Journal of general physiology.

[9]  Henning Scheich,et al.  The Jamming Avoidance Response of High Frequency Electric Fish , 1972 .

[10]  Donald E. Gustafson,et al.  ECG/VCG Rhythm Diagnosis Using Statistical Signal Analysis-I. Identification of Persistent Rhythms , 1978, IEEE Transactions on Biomedical Engineering.

[11]  J. Miller,et al.  Rapid killing of single neurons by irradiation of intracellularly injected dye. , 1979, Science.

[12]  M. F. Johnston,et al.  Interaction of anaesthetics with electrical synapses , 1980, Nature.

[13]  T. Szabo,et al.  Identification of different cell types in the command (pacemaker) nucleus of several gymnotiform species by retrograde transport of horseradish peroxidase , 1980, Neuroscience.

[14]  Identification of different cells types in the command (pacemaker) nucleus of several gynotiform species by retrograde transport of horseradish peroxidase. , 1980, Neuroscience.

[15]  J. T. Enright Temporal precision in circadian systems: a reliable neuronal clock from unreliable components? , 1980, Science.

[16]  D. Spray,et al.  Physiology and pharmacology of gap junctions. , 1985, Annual review of physiology.

[17]  C. Carr,et al.  A time-comparison circuit in the electric fish midbrain. I. Behavior and physiology , 1986, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[18]  A. Winfree When time breaks down , 1987 .

[19]  C. Carr A time comparison circuit in the electric fish midbrain , 1987 .

[20]  L. Maler,et al.  Gap junction protein in weakly electric fish (gymnotide): Immunohistochemical localization with emphasis on structures of the electrosensory system , 1989, The Journal of comparative neurology.

[21]  C H Keller,et al.  Different classes of glutamate receptors mediate distinct behaviors in a single brainstem nucleus. , 1989, Proceedings of the National Academy of Sciences of the United States of America.

[22]  S. Strogatz,et al.  Phase diagram for the collective behavior of limit-cycle oscillators. , 1990, Physical review letters.

[23]  E. Marder,et al.  The effect of electrical coupling on the frequency of model neuronal oscillators. , 1990, Science.

[24]  W. Heiligenberg,et al.  Different classes of glutamate receptors and GABA mediate distinct modulations of a neuronal oscillator, the medullary pacemaker of a gymnotiform electric fish , 1990, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[25]  Walter Heiligenberg,et al.  Neural Nets in Electric Fish , 1991 .

[26]  W. Heiligenberg,et al.  Development of the jamming avoidance response and its morphological correlates in the gymnotiform electric fish, Eigenmannia. , 1992, Journal of neurobiology.

[27]  R. Yuste,et al.  Extensive dye coupling between rat neocortical neurons during the period of circuit formation , 1993, Neuron.

[28]  W. Metzner The jamming avoidance response in Eigenmannia is controlled by two separate motor pathways , 1993, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[29]  Bifurcations of the respiratory pattern associated with reduced lung volume in the rat. , 1993, Journal of applied physiology.

[30]  W. R. Lieb,et al.  Molecular and cellular mechanisms of general anaesthesia , 1994, Nature.

[31]  Y. S. Lee,et al.  Appearance of phase-locked Wenckebach-like rhythms, devil's staircase and universality in intracellular calcium spikes in non-excitable cell models. , 1995, Journal of theoretical biology.

[32]  Y. Yaari,et al.  Effects of Halothane on Glutamate Receptor-mediated Excitatory Postsynaptic Currents: A Patch-Clamp Study in Adult Mouse Hippocampal Slices , 1995, Anesthesiology.

[33]  N. Syed,et al.  A technique for the primary dissociation of neurons from restricted regions of the vertebrate CNS , 1995, Journal of Neuroscience Methods.

[34]  R. W. Turner,et al.  Localization of nicotinamide adenine dinucleotide phosphate‐diaphorase activity in electrosensory and electromotor systems of a gymnotiform teleost, Apteronotus leptorhynchus , 1995, The Journal of comparative neurology.

[35]  A. Mikulec,et al.  Volatile Anesthetics Depress Glutamate Transmission Via Presynaptic Actions , 1996, Anesthesiology.

[36]  R. Pearce Volatile anaesthetic enhancement of paired‐pulse depression investigated in the rat hippocampus in vitro. , 1996, The Journal of physiology.

[37]  Y. Yaari,et al.  Halothane Blocks Synaptic Excitation of Inhibitory Interneurons , 1996, Anesthesiology.

[38]  A H Bass,et al.  Phenotypic specification of hindbrain rhombomeres and the origins of rhythmic circuits in vertebrates. , 1997, Brain, behavior and evolution.

[39]  J. Feldman,et al.  Bidirectional electrical coupling between inspiratory motoneurons in the newborn mouse nucleus ambiguus. , 1997, Journal of neurophysiology.

[40]  J. Spiro Differential activation of glutamate receptor subtypes on a single class of cells enables a neural oscillator to produce distinct behaviors. , 1997, Journal of neurophysiology.

[41]  C. Wong Afferent and efferent connections of the diencephalic prepacemaker nucleus in the weakly electric fish, Eigenmannia virescens: interactions between the electromotor system and the neuroendocrine axis , 1997, The Journal of comparative neurology.

[42]  J. Simpson,et al.  Microcircuitry and function of the inferior olive , 1998, Trends in Neurosciences.

[43]  Lawrence C. Katz,et al.  Relationship between Dye Coupling and Spontaneous Activity in Developing Ferret Visual Cortex , 1998, Developmental Neuroscience.

[44]  J. Juranek,et al.  Segregation of Behavior-Specific Synaptic Inputs to a Vertebrate Neuronal Oscillator , 1998, The Journal of Neuroscience.

[45]  R. Traub,et al.  Electrical coupling underlies high-frequency oscillations in the hippocampus in vitro , 1998, Nature.

[46]  T. Sejnowski,et al.  Submicrosecond pacemaker precision is behaviorally modulated: the gymnotiform electromotor pathway. , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[47]  R. Traub,et al.  High-frequency population oscillations are predicted to occur in hippocampal pyramidal neuronal networks interconnected by axoaxonal gap junctions , 1999, Neuroscience.

[48]  Carson C. Chow,et al.  Dynamics of Spiking Neurons with Electrical Coupling , 2000, Neural Computation.

[49]  T. Sejnowski,et al.  Gap junction effects on precision and frequency of a model pacemaker network. , 2000, Journal of neurophysiology.