Unequal diameters and their effects on time-varying voltages in branched neurons.

A theoretical method, developed in a previous paper, enables one to calculate analytical expressions for time-varying voltages at specific locations in branching dendritic systems in response to synaptic current inputs at other sites. Exact results were obtained for a number of dendritic trees that possessed certain symmetries: all branch lengths had to be integral multiples of one another, and all branch diameters had to be equal. Because the second of these conditions is unrealistic, the method has been generalized to treat dendritic trees whose branches differ in diameter. The method entails adding onto the symmetric results a sum of correction terms. It is found that the correction terms, as well as the symmetric results, can be expressed as combinations of two families of functions. These functions, generalizations of those found in our earlier paper, provide a precise formalism for analyzing how voltage transients depend on the geometrical structure of the dendritic tree. Examples are given that show how the correction terms affect the value of the voltage, and how variations in branch diameters alter the behavior of the propagated postsynaptic potential. The implications of these results for our understanding of neuronal functioning are discussed.

[1]  W. Rall Distinguishing theoretical synaptic potentials computed for different soma-dendritic distributions of synaptic input. , 1967, Journal of neurophysiology.

[2]  Purpura Dp Dendritic differentiation in human cerebral cortex: normal and aberrant developmental patterns. , 1975 .

[3]  D. Durand,et al.  Modelling the postsynaptic location and magnitude of tonic conductance changes resulting from neurotransmitters or drugs , 1981, Neuroscience.

[4]  G. Shepherd The Synaptic Organization of the Brain , 1979 .

[5]  K. Pribram Languages of the Brain: Experimental Paradoxes and Principles in Neuropsychology , 1971 .

[6]  S. Redman The attenuation of passively propagating dendritic potentials in a motoneurone cable model , 1973, The Journal of physiology.

[7]  T. Bliss,et al.  Long‐lasting potentiation of synaptic transmission in the dentate area of the anaesthetized rabbit following stimulation of the perforant path , 1973, The Journal of physiology.

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

[9]  W. Rall Theory of Physiological Properties of Dendrites , 1962, Annals of the New York Academy of Sciences.

[10]  J Rinzel,et al.  Branch input resistance and steady attenuation for input to one branch of a dendritic neuron model. , 1973, Biophysical journal.

[11]  M. Diamond,et al.  A golgi study of dendritic morphology in the occipital cortex of socially reared aged rats , 1981, Experimental Neurology.

[12]  D. Hubel,et al.  The period of susceptibility to the physiological effects of unilateral eye closure in kittens , 1970, The Journal of physiology.

[13]  B. Horwitz Neuronal plasticity: how changes in dendritic architecture can affect the spread of postsynaptic potentials , 1981, Brain Research.

[14]  P. Rakić Local circuit neurons. , 1975, Neurosciences Research Program bulletin.

[15]  R. Llinás,et al.  Electrophysiological properties of dendrites and somata in alligator Purkinje cells. , 1971, Journal of neurophysiology.

[16]  W Rall,et al.  Dendritic location of synapses and possible mechanisms for the monosynaptic EPSP in motoneurons. , 1967, Journal of neurophysiology.

[17]  F. Oberhettinger,et al.  Tables of Laplace Transforms , 1973 .

[18]  Eugene P. Wigner,et al.  Formulas and Theorems for the Special Functions of Mathematical Physics , 1966 .

[19]  B Horwitz,et al.  An analytical method for investigating transient potentials in neurons with branching dendritic trees. , 1981, Biophysical journal.