Pleiotropic effects of SCZ-associated genes (Mäki-Marttunen et al. 2017)

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Accession:187615
Python and MATLAB scripts for studying the dual effects of SCZ-related genes on layer 5 pyramidal cell firing and sinoatrial node cell pacemaking properties. The study is based on two L5PC models (Hay et al. 2011, Almog & Korngreen 2014) and SANC models (Kharche et al. 2011, Severi et al. 2012).
Reference:
1 . Mäki-Marttunen T, Lines GT, Edwards AG, Tveito A, Dale AM, Einevoll GT, Andreassen OA (2017) Pleiotropic effects of schizophrenia-associated genetic variants in neuron firing and cardiac pacemaking revealed by computational modeling. Transl Psychiatry 7:5 [PubMed]
Citations  Citation Browser
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 L5/6 pyramidal GLU cell; Cardiac atrial cell;
Channel(s): I Na,p; I Na,t; I L high threshold; I T low threshold; I A; I K; I M; I h; I K,Ca; I Sodium; I Calcium; I Potassium; I A, slow; Na/Ca exchanger; I_SERCA; Na/K pump; Kir;
Gap Junctions:
Receptor(s):
Gene(s): Nav1.1 SCN1A; Cav3.3 CACNA1I; Cav1.3 CACNA1D; Cav1.2 CACNA1C;
Transmitter(s):
Simulation Environment: NEURON; MATLAB; Python;
Model Concept(s): Schizophrenia;
Implementer(s): Maki-Marttunen, Tuomo [tuomomm at uio.no];
Search NeuronDB for information about:  Neocortex L5/6 pyramidal GLU cell; I Na,p; I Na,t; I L high threshold; I T low threshold; I A; I K; I M; I h; I K,Ca; I Sodium; I Calcium; I Potassium; I A, slow; Na/Ca exchanger; I_SERCA; Na/K pump; Kir;
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pleiotropy
almog
cells
BK.mod *
ca_h.mod
ca_r.mod
cad.mod *
epsp.mod *
ih.mod *
kfast.mod
kslow.mod
na.mod
SK.mod *
best.params *
calcifcurves.py
calcsteadystate.py
cc_run.hoc *
collectfig1.py
collectfig2.py
fig1_curves.mat
fig2_curves.mat
findDCshortthreshold.py
main.hoc *
model.hoc *
mosinit.hoc *
mutation_stuff.py
myrun.hoc *
mytools.py *
params.hoc *
runme.sh *
scalings.sav
                            
:modified 1/7/2007 by Chris Deister for the GP neuron (to remove some of the background current that existed in Mercer 2007)

NEURON {
	SUFFIX sk
	USEION k READ ek WRITE ik
        USEION ca READ cai
        RANGE  gbar,gkahp,ik, inf,tau,g
        GLOBAL Cq10
}

UNITS {
	(mA) = (milliamp)
	(mV) = (millivolt)
	(molar) = (1/liter)
	(mM) = (millimolar)
	(pS) = (picosiemens)
	(um) = (micron)
}

PARAMETER {
	gbar = 0	(pS/um2)
        n = 4
        cai = 50.e-6	(mM)
        b0inv = 16.6666667	(ms)			:1/b0
	celsius = 37	(degC)
	offc = 0.04635023	(mM)                    :(b0/a0)^4
	sloc = 4.0
	Cq10 = 3
}

STATE {	w }

ASSIGNED {
	ik	(mA/cm2)
        g	(pS/um2)
        inf
        tau	(ms)
	a	(1/ms)
        v	(mV)
        ek	(mV)
}

BREAKPOINT {
	SOLVE state METHOD cnexp
	g = gbar*w
	ik = (1e-4)* g*(v-ek)
}

INITIAL {
	rate(cai)
	w=inf
}

DERIVATIVE state {
	rate(cai)
	w' = (inf - w)/tau
}

PROCEDURE rate(cai (mM)) {
	LOCAL q10
	q10 = Cq10^((celsius - 22 (degC))/10 (degC) )
	tau = q10*b0inv/(1+(cai/offc)^sloc)
	inf = 1/(1+(offc/cai)^sloc)
}