Literature DB >> 3900806

The function of dendritic spines: a theoretical study.

F Pongrácz.   

Abstract

A modeling procedure is proposed which introduces the cable equivalent of dendritic spines into the Rall model of spiny interneurons in the spinal cord. At this point combined morphological and physiological works have given some insight into the possible role of a single spine and the function of a single spine has been studied by theoretical computations [Jack, Noble and Tsien (1975) Electric Current Flow in Excitable Cells, pp. 218-223. Oxford University Press, Oxford; Koch and Poggio (1983) Trends Neurosci. 6, 80-83; Perkel (1983) J. Physiol., Paris 78, 695-699]. The goal of the present paper is two-fold: (a) to stress the gross function of the spine system in the excitability of dendrites; and (b) to emphasize the role of spines in the dynamic input/output function of neurons. The simulation procedure is based on the well-known compartmental method. (1) The kinetics of active somatic and dendritic compartments are taken from a currently available spinal interneuron model to match the physiological data of large dorsal horn neurons carrying spines. (2) Beside the prolongation of the somatic excitatory postsynaptic potential, the model suggests that the spiny neuron increases the differences in the latency and height of excitatory postsynaptic potential as a function of the electrotonic position of input. The characteristics of the excitatory postsynaptic potential can be modified by the changes in spine geometry and the ratio of cytoplasmic resistances of spine stalk to that of main dendritic shaft. (3) Dendritic electroresponsiveness, which was already postulated for dorsal horn neurons, is analysed by the model including calcium and slow potassium systems. It is concluded that the participation of the spine stalk in active processes can highly modify the input dependence of response pattern. Depolarization-dependent Ca2+ accumulation in spines may reflect the interaction of spine stalks. (4) Passive antidromic spread of action potential can be suppressed in spiny cells. Analysis of active antidromic spread shows the probable importance of spines located near the soma. Centripetal vs centrifugal conduction of dendritic action potential may depend on the spine distribution along the tree and change in electrical parameters of spines.

Entities:  

Mesh:

Substances:

Year:  1985        PMID: 3900806     DOI: 10.1016/0306-4522(85)90244-1

Source DB:  PubMed          Journal:  Neuroscience        ISSN: 0306-4522            Impact factor:   3.590


  7 in total

1.  A model of NMDA receptor-mediated activity in dendrites of hippocampal CA1 pyramidal neurons.

Authors:  F Pongrácz; N P Poolos; J D Kocsis; G M Shepherd
Journal:  J Neurophysiol       Date:  1992-12       Impact factor: 2.714

2.  Maladaptive dendritic spine remodeling contributes to diabetic neuropathic pain.

Authors:  Andrew M Tan; Omar A Samad; Tanya Z Fischer; Peng Zhao; Anna-Karin Persson; Stephen G Waxman
Journal:  J Neurosci       Date:  2012-05-16       Impact factor: 6.167

3.  Synaptic targets of HRP-filled layer III pyramidal cells in the cat striate cortex.

Authors:  Z F Kisvárday; K A Martin; T F Freund; Z Maglóczky; D Whitteridge; P Somogyi
Journal:  Exp Brain Res       Date:  1986       Impact factor: 1.972

4.  Dendritic spine dysgenesis contributes to hyperreflexia after spinal cord injury.

Authors:  Samira P Bandaru; Shujun Liu; Stephen G Waxman; Andrew M Tan
Journal:  J Neurophysiol       Date:  2014-12-10       Impact factor: 2.714

5.  Dendritic spine remodeling following early and late Rac1 inhibition after spinal cord injury: evidence for a pain biomarker.

Authors:  Peng Zhao; Myriam Hill; Shujun Liu; Lubin Chen; Lakshmi Bangalore; Stephen G Waxman; Andrew M Tan
Journal:  J Neurophysiol       Date:  2016-03-02       Impact factor: 2.714

6.  Dendritic spine dysgenesis in superficial dorsal horn sensory neurons after spinal cord injury.

Authors:  Xiaoyu C Cao; Laura W Pappalardo; Stephen G Waxman; Andrew M Tan
Journal:  Mol Pain       Date:  2017-01       Impact factor: 3.395

7.  Therapeutic potential of Pak1 inhibition for pain associated with cutaneous burn injury.

Authors:  Yiqun Guo; Curtis Benson; Myriam Hill; Stefanie Henry; Philip Effraim; Stephen G Waxman; Sulayman Dib-Hajj; Andrew M Tan
Journal:  Mol Pain       Date:  2018-06-29       Impact factor: 3.395

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.