Literature DB >> 2313349

Voltage behavior along the irregular dendritic structure of morphologically and physiologically characterized vagal motoneurons in the guinea pig.

R Nitzan1, I Segev, Y Yarom.   

Abstract

1. Intracellular recordings from neurons in the dorsal motor nucleus of the vagus (vagal motoneurons, VMs) obtained in the guinea pig brain stem slice preparation were used for both horseradish peroxidase (HRP) labeling of the neurons and for measurements of their input resistance (RN) and time constant (tau 0). Based on the physiological data and on the morphological reconstruction of the labeled cells, detailed steady-state and compartmental models of VM were built and utilized to estimate the range of membrane resistivity, membrane capacitance, and cytoplasm resistivity values (Rm, Cm, and Ri, respectively) and to explore the integrative properties of these cells. 2. VMs are relatively small cells with a simple dendritic structure. Each cell has an average of 5.3 smooth (nonspiny), short (251 microns) dendrites with a low order (2) of branching. The average soma-dendritic surface area of VMs is 9,876 microns 2. 3. Electrically, VMs show remarkably linear membrane properties in the hyperpolarizing direction; they have an average RN of 67 +/- 23 (SD) M omega and a tau 0 of 9.4 +/- 4.1 ms. Several unfavorable experimental conditions precluded the possibility of faithfully recovering ("peeling") the first equalizing time constant (tau 1) and, thereby, of estimating the electrotonic length (Lpeel) of VMs. 4. Reconciling VM morphology with the measured RN and tau 0 through the models, assuming an Ri of 70 omega.cm and a spatially uniform Rm, yielded an Rm estimate of 5,250 omega.cm2 and a Cm of 1.8 microF/cm2. Peeling theoretical transients produced by these models result in an Lpeel of 1.35. Because of marked differences in the length of dendrites within a single cell, this value is larger than the maximal cable length of the dendrites and is twice as long as their average cable length. 5. The morphological and physiological data could be matched indistinguishably well if a possible soma shunt (i.e., Rm, soma less than Rm, dend) was included in the model. Although there is no unique solution for the exact model Rm, a general conclusion regarding the integrative capabilities of VM could be drawn. As long as the model is consistent with the experimental data, the average input resistance at the dendritic terminals (RT) and the steady-state central (AFT----S) and peripheral (AFS----T) attenuation factors are essentially the same in the different models. With Ri = 70 omega.cm, we calculated RT, AFS----T, and AFT----S to be, on the average, 580 M omega, 1.1, and 13, respectively.(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1990        PMID: 2313349     DOI: 10.1152/jn.1990.63.2.333

Source DB:  PubMed          Journal:  J Neurophysiol        ISSN: 0022-3077            Impact factor:   2.714


  12 in total

1.  Signals in stochastically generated neurons.

Authors:  J L Winslow; S F Jou; S Wang; J M Wojtowicz
Journal:  J Comput Neurosci       Date:  1999-01       Impact factor: 1.621

2.  Modelling the electrotonic structure of starburst amacrine cells in the rabbit retina: a functional interpretation of dendritic morphology.

Authors:  R R Poznanski
Journal:  Bull Math Biol       Date:  1992-11       Impact factor: 1.758

3.  Monosynaptic EPSPs elicited by single interneurones and spindle afferents in trigeminal motoneurones of anaesthetized rats.

Authors:  P D Grimwood; K Appenteng; J C Curtis
Journal:  J Physiol       Date:  1992-09       Impact factor: 5.182

4.  Derivation of cable parameters for a reduced model that retains asymmetric voltage attenuation of reconstructed spinal motor neuron dendrites.

Authors:  Hojeong Kim; Lora A Major; Kelvin E Jones
Journal:  J Comput Neurosci       Date:  2009-04-22       Impact factor: 1.621

5.  A novel theoretical approach to the analysis of dendritic transients.

Authors:  H Agmon-Snir
Journal:  Biophys J       Date:  1995-11       Impact factor: 4.033

6.  Electrical consequences of spine dimensions in a model of a cortical spiny stellate cell completely reconstructed from serial thin sections.

Authors:  I Segev; A Friedman; E L White; M J Gutnick
Journal:  J Comput Neurosci       Date:  1995-06       Impact factor: 1.621

Review 7.  Solutions for transients in arbitrarily branching cables: I. Voltage recording with a somatic shunt.

Authors:  G Major; J D Evans; J J Jack
Journal:  Biophys J       Date:  1993-07       Impact factor: 4.033

8.  Physiology, morphology and detailed passive models of guinea-pig cerebellar Purkinje cells.

Authors:  M Rapp; I Segev; Y Yarom
Journal:  J Physiol       Date:  1994-01-01       Impact factor: 5.182

9.  Ionic basis of membrane potential changes induced by anoxia in rat dorsal vagal motoneurones.

Authors:  A I Cowan; R L Martin
Journal:  J Physiol       Date:  1992-09       Impact factor: 5.182

10.  An analysis of the long-lasting after-hyperpolarization of guinea-pig vagal motoneurones.

Authors:  S D Hocherman; R Werman; Y Yarom
Journal:  J Physiol       Date:  1992-10       Impact factor: 5.182

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