Effects of spinal cord stimulation on WDR dorsal horn network (Zhang et al 2014)

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Accession:168414
" ... To study the mechanisms underlying SCS (Spinal cord stimulation), we constructed a biophysically-based network model of the dorsal horn circuit consisting of interconnected dorsal horn interneurons and a wide dynamic range (WDR) projection neuron and representations of both local and surround receptive field inhibition. We validated the network model by reproducing cellular and network responses relevant to pain processing including wind-up, A-fiber mediated inhibition, and surround receptive field inhibition. ..." See paper for more.
Reference:
1 . Zhang TC, Janik JJ, Grill WM (2014) Modeling effects of spinal cord stimulation on wide-dynamic range dorsal horn neurons: influence of stimulation frequency and GABAergic inhibition. J Neurophysiol 112:552-67 [PubMed]
Model Information (Click on a link to find other models with that property)
Model Type: Realistic Network;
Brain Region(s)/Organism:
Cell Type(s): Wide dynamic range neuron;
Channel(s):
Gap Junctions:
Receptor(s): GabaA; AMPA; NMDA; Glutamate; Glycine;
Gene(s):
Transmitter(s):
Simulation Environment: NEURON;
Model Concept(s):
Implementer(s): Zhang, Tianhe [tz5@duke.edu];
Search NeuronDB for information about:  GabaA; AMPA; NMDA; Glutamate; Glycine;
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ZhangEtAl2014
Critical Mod Files
AMPA_DynSyn.mod
B_A.mod
B_Adapt.mod
B_DR.mod
B_NA.mod
CaIntraCellDyn.mod *
GABAa_DynSyn.mod *
GABAb_DynSyn.mod *
Glycine_DynSyn.mod
HH2.mod *
HH2new.mod *
iCaAN.mod *
iCaL.mod
iKCa.mod *
iNaP.mod *
KDR.mod
KDRI.mod
NK1_DynSyn.mod *
NMDA_DynSyn.mod *
SS.mod
vsource.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
:
:
: 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
:
: "The normal resting [Ca2+]i lies in the range of 30 to 200 nM 
: in living cells." (Hille 2001)
: Parameter changes by Paulo Aguiar and Mafalda Sousa, IBMC, May 2008
: pauloaguiar@fc.up.pt; mafsousa@ibmc.up.pt



INDEPENDENT {t FROM 0 TO 1 WITH 1 (ms)}

NEURON {
	SUFFIX CaIntraCellDyn
	USEION ca READ ica, cai WRITE cai	
        RANGE cai_new, depth, cai_inf, cai_tau
}

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


PARAMETER {
	depth	= 0.1	  (um)		: depth of shell
	cai_tau	= 2.0     (ms)		: rate of calcium removal
	cai_inf	= 50.0e-6 (mM)		: equilibrium intracellular calcium concentration
	cai		  (mM)
}

STATE {
	cai_new		(mM) 
}

INITIAL {

	cai_new = cai_inf
}

ASSIGNED {
	ica		(mA/cm2)
	drive_channel	(mM/ms)
}
	
BREAKPOINT {
	SOLVE state METHOD euler
}

DERIVATIVE state { 

	drive_channel =  - (10000) * ica / (2 * FARADAY * depth)
	if (drive_channel <= 0.) { drive_channel = 0.  }   : cannot pump inward 
         
	cai_new' = drive_channel + (cai_inf-cai_new)/cai_tau
	cai = cai_new
}

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