Efficient mapping from neuroanatomical to electrotonic space

Previous studies documented the importance of electrotonic structure in single-neuron computations. Here we elaborate a new approach to electrotonic theory and analysis. We begin with a more versatile measure Lij of the electrotonic distance between any two locations i and j on a neuron. If Vi is the voltage at the origin and Vj is the voltage at Some other point, the electrotonic distance is Lij=ln(Vi/Vj). Voltage decays e-fold per unit of L for any two points on the neuron, regardless of its electrotonic architecture. Lij increases as the sinusoidal frequency of Vi increases. If j lies on the direct path between i and k, then Lik=Lij+Ljk. This relation enables electrotonic transforms of the neuron—graphical mappings from neuroanatomical to electrotonic space. For each neuron, there exists an infinite number of such transforms, which can be done from any reference location on the neuron, as a function of voltage transfer to or from that location, and for any frequency of input signal. Sets of these trans...

[1]  J. Jack,et al.  Electric current flow in excitable cells , 1975 .

[2]  D. Perkel,et al.  Calibrating compartmental models of neurons. , 1978, The American journal of physiology.

[3]  T. H. Brown,et al.  Passive electrical constants in three classes of hippocampal neurons. , 1981, Journal of neurophysiology.

[4]  N T Carnevale,et al.  Electrophysiological characterization of remote chemical synapses. , 1982, Journal of neurophysiology.

[5]  T. H. Brown,et al.  Interpretation of voltage-clamp measurements in hippocampal neurons. , 1983, Journal of neurophysiology.

[6]  M. Hines,et al.  Efficient computation of branched nerve equations. , 1984, International journal of bio-medical computing.

[7]  Segal Sj NORPLANT contraceptive implants advancing. , 1984 .

[8]  T. H. Brown,et al.  Conductance mechanism responsible for long-term potentiation in monosynaptic and isolated excitatory synaptic inputs to hippocampus. , 1986, Journal of neurophysiology.

[9]  D. Amaral,et al.  A light and electron microscopic analysis of the mossy fibers of the rat dentate gyrus , 1986, The Journal of comparative neurology.

[10]  Elaine S. Oran,et al.  Numerical Simulation of Reactive Flow , 1987 .

[11]  M Hines,et al.  A program for simulation of nerve equations with branching geometries. , 1989, International journal of bio-medical computing.

[12]  G. Shepherd,et al.  Comparisons between Active Properties of Distal Dendritic Branches and Spines: Implications for Neuronal Computations , 1989, Journal of Cognitive Neuroscience.

[13]  E. W. Kairiss,et al.  Hebbian synapses: biophysical mechanisms and algorithms. , 1990, Annual review of neuroscience.

[14]  C F Stevens,et al.  Two different ways evolution makes neurons larger. , 1990, Progress in brain research.

[15]  D. Johnston,et al.  Induction of long-term potentiation at hippocampal mossy-fiber synapses follows a Hebbian rule. , 1990, Journal of neurophysiology.

[16]  Anthony M. Zador,et al.  Self-organization of Hebbian Synapses in Hippocampal Neurons , 1990, NIPS.

[17]  W M Cowan,et al.  Quantitative, three‐dimensional analysis of granule cell dendrites in the rat dentate gyrus , 1990, The Journal of comparative neurology.

[18]  B. Claiborne,et al.  Dendritic growth and regression in rat dentate granule cells during late postnatal development. , 1990, Brain research. Developmental brain research.

[19]  Anthony M. Zador,et al.  Hebbian computations in hippocampal dendrites and spines , 1992 .

[20]  Brenda J. Claiborne,et al.  Use of Computers for Quantitative, Three-Dimensional Analysis of Dendritic Trees , 1992 .

[21]  Edward W. Kairiss,et al.  Dendritic Control of Hebbian Computations , 1992 .

[22]  Anthony M. Zador,et al.  Computational models of hippocampal neurons , 1992 .

[23]  D. Johnston,et al.  NMDA-receptor-independent long-term potentiation. , 1992, Annual review of physiology.

[24]  N. Spruston,et al.  Perforated patch-clamp analysis of the passive membrane properties of three classes of hippocampal neurons. , 1992, Journal of neurophysiology.

[25]  B. Claiborne,et al.  Morphology of intracellularly labeled interneurons in the dentate gyrus of the immature rat , 1992, The Journal of comparative neurology.

[26]  William R. Holmes,et al.  Electrotonic models of neuronal dendrites and single neuron computation , 1992 .

[27]  Michael L. Hines,et al.  NEURON — A Program for Simulation of Nerve Equations , 1993 .

[28]  T. H. Brown,et al.  Hippocampal circuitry complicates analysis of long‐term potentiation in mossy fiber synapses , 1993, Hippocampus.

[29]  N. Spruston,et al.  Voltage- and space-clamp errors associated with the measurement of electrotonically remote synaptic events. , 1993, Journal of neurophysiology.

[30]  T. H. Brown,et al.  Confocal laser scanning microscopy reveals voltage-gated calcium signals within hippocampal dendritic spines. , 1994, Journal of neurobiology.

[31]  Nicholas T. Carnevale,et al.  Hebbian learning is jointly controlled by electrotonic and input structure , 1994 .

[32]  D. H. Edwards,et al.  Changes in synaptic integration during the growth of the lateral giant neuron of crayfish. , 1994, Journal of neurophysiology.

[33]  Michael L. Hines,et al.  The Neuron Simulation Program , 1994 .

[34]  T. H. Brown,et al.  Confocal imaging of dendritic Ca2+ transients in hippocampal brain slices during simultaneous current‐ and voltage‐clamp recording , 1994, Microscopy research and technique.

[35]  A. C. Greenwood,et al.  Quantal mechanism of long-term potentiation in hippocampal mossy-fiber synapses. , 1994, Journal of neurophysiology.

[36]  Nicholas T. Carnevale,et al.  Qualitative Electrotonic Comparison of Three Classes of Hippocampal Neurons in the Rat , 1995 .