Literature DB >> 2213137

Computer simulation of group Ia EPSPs using morphologically realistic models of cat alpha-motoneurons.

I Segev1, J W Fleshman, R E Burke.   

Abstract

1. Morphological and electrophysiological data on the electrotonic structure of six triceps surae alpha-motoneurons and on the number and location of 202 Group Ia synapses making contact with ankle extensor motoneurons, previously obtained in this laboratory, were used to construct computer models to examine the generation of composite monosynaptic Group Ia excitatory postsynaptic potentials (EPSPs). 2. A total of 300 active synapses, each generating conductance transients based on voltage-clamp data and having activation times temporally dispersed (range approximately 1.3 ms) according to the conduction velocity profile of Group Ia-afferents, were used to generate composite EPSPs. 3. The shape indexes (foot-to-peak rise times and half widths) of simulated EPSPs matched those of experimentally observed Ia EPSPs reasonably well, although the rise times were, on average, approximately 0.25 ms longer in the simulated EPSPs. This may indicate that the effective temporal dispersion of actual Group Ia monosynaptic EPSPs is less than that the temporal asynchrony used in the simulations. 4. The peak amplitudes of simulated composite EPSPs (6-14 mV), as well as EPSPs produced by single somatic synapses (80-300 microV), were comparable to those found in experimental data. 5. Simulated EPSPs in motoneuron models with two forms of nonuniform Rm distribution ("step" increase from low values of Rm on the soma to much higher but uniform values in the dendrites, versus gradual monotonic "sigmoidal" increases from soma to distal dendrites) were similar in shape and amplitude. This prevented choosing one or the other Rm model as more "correct." 6. Transmembrane voltages at synaptic sites in motoneuron dendrites during generation of composite Ia EPSPs had peak amplitudes less than twice those of the somatic EPSP. The amount of nonlinearity during EPSP production was assessed by making the delivery of synaptic current independent of the local transmembrane voltage. This non-linearity was modest (less than 10%) during composite EPSP generation, consistent with previous experimental evidence. 7. The local voltages produced in various parts of different dendrites during composite EPSP generation depended on the number and location of active synapses and on the electrotonic structure of the particular dendrite. The results show that dendrites that project in different directions away from the motoneuron soma could, in principle, exhibit different degrees of interaction between Ia and other synaptic inputs. 8. Although produced by the same number of active synapses, the simulated composite Ia EPSPs varied over a two-fold range of peak amplitude in relation to motor-unit type, cell input resistance, and cell size (total membrane area).(ABSTRACT TRUNCATED AT 400 WORDS)

Mesh:

Year:  1990        PMID: 2213137     DOI: 10.1152/jn.1990.64.2.648

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


  25 in total

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2.  Comparison of alternative designs for reducing complex neurons to equivalent cables.

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

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Journal:  J Comput Neurosci       Date:  2009-04-22       Impact factor: 1.621

6.  The effects of model composition design choices on high-fidelity simulations of motoneuron recruitment and firing behaviors.

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7.  Simulation of Ca2+ persistent inward currents in spinal motoneurones: mode of activation and integration of synaptic inputs.

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8.  The transformation of synaptic to system plasticity in motor output from the sacral cord of the adult mouse.

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Journal:  J Neurophysiol       Date:  2015-07-22       Impact factor: 2.714

9.  Development of modified cable models to simulate accurate neuronal active behaviors.

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Journal:  J Appl Physiol (1985)       Date:  2014-10-02

10.  The recurrent case for the Renshaw cell.

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