Propagation of dendritic spikes mediated by excitable spines: a continuum theory.

1. Neuroscientists are currently hypothesizing on how voltage-dependent channels, in dendrites with spines, may be spatially distributed or how their numbers may divide between spine heads and the dendritic base. A new cable theory is formulated to investigate electrical interactions between many excitable and/or passive dendritic spines. The theory involves a continuum formulation in which the spine density, the membrane potential in spine heads, and the spine stem current vary continuously in space and time. The spines, however, interact only indirectly by voltage spread along the dendritic shaft. Active membrane in the spine heads is modeled with Hodgkin-Huxley (HH) kinetics. Synaptic currents are generated by transient conductance increases. For most simulations the membrane of spine stems and dendritic shaft is assumed passive. 2. Action-potential generation and propagation occur as localized excitatory synaptic input into spine heads causes a few excitable spines to fire, which then initiates a chain reaction of spine firings along a branch. This sustained wavelike response is possible for a certain range of spine densities and electrical parameters. Propagation is precluded for spine stem resistance (Rss) either too large or too small. Moreover, even if Rss lies in a suitable range for the local generation of an action potential (resulting from local synaptic excitatory input), this range may not be suitable to initiate a chain reaction of spine firings along the dendrite; success or failure of impulse propagation depends on an even narrower range of Rss values. 3. The success or failure of local excitation to spread as a chain reaction depends on the spatial distribution of spines. Impulse propagation is unlikely if the excitable spines are spaced too far apart. However, propagation may be recovered by redistributing the same number of equally spaced spines into clusters. 4. The spread of excitation in a distal dendritic arbor is also influenced by the branching geometry. Input to one branch can initiate a chain reaction that accelerates into the sister branch but rapidly attenuates as it enters the parent branch. In branched dendrites with many excitable and passive spines, regions of decreased conductance load (e.g., near sealed ends) can facilitate attenuating waves and enhance waves that are successfully propagating. Regions of increased conductance load (e.g., near common branch points) promote attenuation and tend to block propagation. Non-uniform loading and/or nonuniform spine densities can lead to complex propagation characteristics. 5. Some analytic results of classical cable theory are generalized for the case of a passive spiny dendritic cable.(ABSTRACT TRUNCATED AT 400 WORDS)

[1]  T. Powell,et al.  Morphological variations in the dendritic spines of the neocortex. , 1969, Journal of cell science.

[2]  C. Koch,et al.  The dynamics of free calcium in dendritic spines in response to repetitive synaptic input. , 1987, Science.

[3]  M. Colonnier Synaptic patterns on different cell types in the different laminae of the cat visual cortex. An electron microscope study. , 1968, Brain research.

[4]  W. N. Ross,et al.  Mapping calcium transients in the dendrites of Purkinje cells from the guinea‐pig cerebellum in vitro. , 1987, The Journal of physiology.

[5]  E. Fifková,et al.  Long-lasting morphological changes in dendritic spines of dentate granular cells following stimulation of the entorhinal area , 1977, Journal of neurocytology.

[6]  Robert M. Miura,et al.  Some mathematical questions in biology, neurobiology , 1982 .

[7]  W. Greenough,et al.  Experiential modification of the developing brain. , 1975, American scientist.

[8]  E. Gray,et al.  Axo-somatic and axo-dendritic synapses of the cerebral cortex: an electron microscope study. , 1959, Journal of anatomy.

[9]  C. Wilson,et al.  Passive cable properties of dendritic spines and spiny neurons , 1984, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[10]  T. Poggio,et al.  A theoretical analysis of electrical properties of spines , 1983, Proceedings of the Royal Society of London. Series B. Biological Sciences.

[11]  P. Groves,et al.  Three-dimensional structure of dendritic spines in the rat neostriatum , 1983, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[12]  KM Harris,et al.  Dendritic spines of CA 1 pyramidal cells in the rat hippocampus: serial electron microscopy with reference to their biophysical characteristics , 1989, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[13]  W Rall,et al.  Changes of action potential shape and velocity for changing core conductor geometry. , 1974, Biophysical journal.

[14]  D. Perkel,et al.  Dendritic spines: role of active membrane in modulating synaptic efficacy , 1985, Brain Research.

[15]  G. Major,et al.  The modelling of pyramidal neurones in the visual cortex , 1989 .

[16]  Curtis F. Gerald Applied numerical analysis , 1970 .

[17]  W. Levy,et al.  Insights into associative long-term potentiation from computational models of NMDA receptor-mediated calcium influx and intracellular calcium concentration changes. , 1990, Journal of neurophysiology.

[18]  H C Tuckwell,et al.  A mathematical model for spreading cortical depression. , 1978, Biophysical journal.

[19]  Idan Segev,et al.  Compartmental models of complex neurons , 1989 .

[20]  W Rall,et al.  Computational study of an excitable dendritic spine. , 1988, Journal of neurophysiology.

[21]  J. Miller,et al.  Synaptic amplification by active membrane in dendritic spines , 1985, Brain Research.

[22]  K. Harris,et al.  Dendritic spines of rat cerebellar Purkinje cells: serial electron microscopy with reference to their biophysical characteristics , 1988, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[23]  Idan Segev,et al.  Signal enhancement in distal cortical dendrites by means of interactions between active dendritic spines. , 1985, Proceedings of the National Academy of Sciences of the United States of America.

[24]  D H Perkel,et al.  The function of dendritic spines: a review of theoretical issues. , 1985, Behavioral and neural biology.

[25]  John Rinzel,et al.  Neuronal plasticity (learning) , 1982 .

[26]  Gray Eg Axo-somatic and axo-dendritic synapses of the cerebral cortex: An electron microscope study , 1959 .

[27]  Curtis F. Gerald,et al.  APPLIED NUMERICAL ANALYSIS , 1972, The Mathematical Gazette.

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

[29]  A. Hodgkin,et al.  A quantitative description of membrane current and its application to conduction and excitation in nerve , 1990 .

[30]  G. Shepherd,et al.  Computer simulation of a dendrodendritic synaptic circuit for self- and lateral-inhibition in the olfactory bulb , 1979, Brain Research.

[31]  A. Peters,et al.  The small pyramidal neuron of the rat cerebral cortex. The perikaryon, dendrites and spines. , 1970, The American journal of anatomy.

[32]  D. Prince,et al.  Synaptic control of excitability in isolated dendrites of hippocampal neurons , 1984, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[33]  M Kawato,et al.  Electrical properties of dendritic spines with bulbous end terminals. , 1984, Biophysical journal.

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

[35]  G. Yaşargil,et al.  Synaptic function in the fish spinal cord: dendritic integration. , 1969, Progress in brain research.

[36]  E. Fifková,et al.  Swelling of dendritic spines in the fascia dentata after stimulation of the perforant fibers as a mechanism of post-tetanic potentiation , 1975, Experimental Neurology.