Pyramidal neuron coincidence detection tuned by dendritic branching pattern (Schaefer et al 2003)

 Download zip file   Auto-launch 
Help downloading and running models
"... We examined the relationship between dendritic arborization and the coupling between somatic and dendritic action potential (AP) initiation sites in layer 5 (L5) neocortical pyramidal neurons. Coupling was defined as the relative reduction in threshold for initiation of a dendritic calcium AP due to a coincident back-propagating AP. Simulations based on reconstructions of biocytin-filled cells showed that addition of oblique branches of the main apical dendrite in close proximity to the soma (d < 140 um) increases the coupling between the apical and axosomatic AP initiation zones, whereas incorporation of distal branches decreases coupling. ... We conclude that variation in dendritic arborization may be a key determinant of variability in coupling (49+-17%; range 19-83%; n = 37) and is likely to outweigh the contribution made by variations in active membrane properties. Thus coincidence detection of inputs arriving from different cortical layers is strongly regulated by differences in dendritic arborization."
1 . Schaefer AT, Larkum ME, Sakmann B, Roth A (2003) Coincidence detection in pyramidal neurons is tuned by their dendritic branching pattern. J Neurophysiol 89:3143-54 [PubMed]
Model Information (Click on a link to find other models with that property)
Model Type: Neuron or other electrically excitable cell;
Brain Region(s)/Organism:
Cell Type(s): Neocortex V1 L6 pyramidal corticothalamic GLU cell;
Channel(s): I Na,t; I A; I K; I M; I K,Ca; I Calcium;
Gap Junctions:
Simulation Environment: NEURON;
Model Concept(s): Action Potential Initiation; Coincidence Detection;
Implementer(s): Schaefer, Andreas T [andreas.schaefer at];
Search NeuronDB for information about:  Neocortex V1 L6 pyramidal corticothalamic GLU cell; I Na,t; I A; I K; I M; I K,Ca; I Calcium;
cad2.mod *
child.mod *
childa.mod *
epsp.mod *
it2.mod *
kaprox.mod *
kca.mod *
km.mod *
kv.mod *
na.mod *
SlowCa.mod *
TITLE decay of internal calcium concentration
: Internal calcium concentration due to calcium currents and pump.
: Differential equations.
: Simple model of ATPase pump with 3 kinetic constants (Destexhe 92)
:     Cai + P <-> CaP -> Cao + P  (k1,k2,k3)
: A Michaelis-Menten approximation is assumed, which reduces the complexity
: of the system to 2 parameters: 
:       kt = <tot enzyme concentration> * k3  -> TIME CONSTANT OF THE PUMP
:	kd = k2/k1 (dissociation constant)    -> EQUILIBRIUM CALCIUM VALUE
: The values of these parameters are chosen assuming a high affinity of 
: the pump to calcium and a low transport capacity (cfr. Blaustein, 
: TINS, 11: 438, 1988, and references therein).  
: Units checked using "modlunit" -> factor 10000 needed in ca entry
: VERSION OF PUMP + DECAY (decay can be viewed as simplified buffering)
: All variables are range variables
: adopted from the lower model by AS 102199
: This mechanism was published in:  Destexhe, A. Babloyantz, A. and 
: Sejnowski, TJ.  Ionic mechanisms for intrinsic slow oscillations in
: thalamic relay neurons. Biophys. J. 65: 1538-1552, 1993)
: Written by Alain Destexhe, Salk Institute, Nov 12, 1992


	SUFFIX cad2
	USEION ca READ ica, cai WRITE cai
	GLOBAL depth,cainf,taur

	(molar) = (1/liter)			: moles do not appear in units
	(mM)	= (millimolar)
	(um)	= (micron)
	(mA)	= (milliamp)
	(msM)	= (ms mM)
	FARADAY = (faraday) (coulomb)

	depth	= .1	(um)		: depth of shell
	taur	= 80	(ms)		: rate of calcium removal, changed from 200 to 80 (H.Markram)
	cainf	= 100e-6(mM)
	cai		(mM)

	ca		(mM) 

	ca = cainf

	ica		(mA/cm2)
	drive_channel	(mM/ms)
	SOLVE state METHOD euler


	drive_channel =  - (10000) * ica / (2 * FARADAY * depth)
	if (drive_channel <= 0.) { drive_channel = 0. }	: cannot pump inward

	ca' = drive_channel + (cainf-ca)/taur
	cai = ca

Loading data, please wait...