Layer V pyramidal cell functions and schizophrenia genetics (Mäki-Marttunen et al 2019)

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Accession:249463
Study on how GWAS-identified risk genes of shizophrenia affect excitability and integration of inputs in thick-tufted layer V pyramidal cells
Reference:
1 . Mäki-Marttunen T, Devor A, Phillips WA, Dale AM, Andreassen OA, Einevoll GT (2019) Computational modeling of genetic contributions to excitability and neural coding in layer V pyramidal cells: applications to schizophrenia pathology Front. Comput. Neurosci. 13:66
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: Neocortex;
Cell Type(s):
Channel(s): I A; I M; I h; I K,Ca; I Calcium; I A, slow; I Na,t; I Na,p; I L high threshold; I T low threshold;
Gap Junctions:
Receptor(s): AMPA; NMDA; Gaba;
Gene(s):
Transmitter(s): Glutamate; Gaba;
Simulation Environment: NEURON; Python;
Model Concept(s): Schizophrenia; Dendritic Action Potentials; Action Potential Initiation; Synaptic Integration;
Implementer(s): Maki-Marttunen, Tuomo [tuomo.maki-marttunen at tut.fi];
Search NeuronDB for information about:  AMPA; NMDA; Gaba; I Na,p; I Na,t; I L high threshold; I T low threshold; I A; I M; I h; I K,Ca; I Calcium; I A, slow; Gaba; Glutamate;
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l5pc_scz
hay
models
morphologies
README.html
Ca_HVA.mod *
Ca_LVAst.mod *
CaDynamics_E2.mod *
epsp.mod *
Ih.mod *
Im.mod *
K_Pst.mod *
K_Tst.mod *
Nap_Et2.mod *
NaTa_t.mod *
ProbAMPANMDA2.mod *
ProbUDFsyn2.mod *
SK_E2.mod *
SKv3_1.mod *
calcapicalthresholds_control.py
calcapicalthresholds_epsp_control.py
calcifcurves.py
calcifcurves_comb.py
calcnspikesperburst2.py
calcsteadystate.py
calcupdown2responses.py
calcupdownresponses_noisydown.py
calcupdownresponses_noisyup.py
coding.py
coding_comb.py
coding_nonprop_comb_somaticI.py
coding_nonprop_somaticI.py
collectupdownresponses_noisy.py
control_cs.sav
controlamps_cs0.sav
controlamps_cs1.sav
controlamps_cs2.sav
controlamps_cs3.sav
controlamps_cs4.sav
controlamps_cs5.sav
controlamps_cs6.sav
drawfigcomb.py
drawnspikesperburst2.py
drawupdownresponses_noisy.py
findppicoeffs.py
findppicoeffs_comb.py
findppicoeffs_complement.py
findthresholdbasalamps_coding.py
findthresholddistalamps.py
findthresholddistalamps_coding.py
findthresholddistalamps_comb.py
mutation_stuff.py
mytools.py
protocol.py
runcontrols_cs.py
savebasalsynapselocations_coding.py
savesynapselocations.py
savesynapselocations_coding.py
scalemutations_cs.py
scalings_cs.sav
setparams.py
synlocs300.0.sav
                            
:Comment :
:Reference : :		Reuveni, Friedman, Amitai, and Gutnick, J.Neurosci. 1993

NEURON	{
	SUFFIX Ca_HVA
	USEION ca READ eca WRITE ica
	RANGE gCa_HVAbar, gCa_HVA, ica, offma, offmb, offha, offhb, sloma, slomb, sloha, slohb, tauma, taumb, tauha, tauhb
}

UNITS	{
	(S) = (siemens)
	(mV) = (millivolt)
	(mA) = (milliamp)
}

PARAMETER	{
	gCa_HVAbar = 0.00001 (S/cm2) 
        offma = -27 (mV)
        offmb = -75 (mV)
        offha = -13 (mV)
        offhb = -15 (mV)
        sloma = 3.8 (mV)
        slomb = 17 (mV)
        sloha = 50 (mV)
        slohb = 28 (mV)
	tauma = 18.1818 (ms)
	taumb = 1.06383 (ms)
	tauha = 2188.18 (ms)
	tauhb = 153.846 (ms)
}

ASSIGNED	{
	v	(mV)
	eca	(mV)
	ica	(mA/cm2)
	gCa_HVA	(S/cm2)
	mInf
	mTau
	mAlpha
	mBeta
	hInf
	hTau
	hAlpha
	hBeta
}

STATE	{ 
	m
	h
}

BREAKPOINT	{
	SOLVE states METHOD cnexp
	gCa_HVA = gCa_HVAbar*m*m*h
	ica = gCa_HVA*(v-eca)
}

DERIVATIVE states	{
	rates()
	m' = (mInf-m)/mTau
	h' = (hInf-h)/hTau
}

INITIAL{
	rates()
	m = mInf
	h = hInf
}

PROCEDURE rates(){
	UNITSOFF
        if((v == offma) ){        
            v = v+0.0001
        }
		mAlpha =  (offma-v)/tauma/(exp((offma-v)/sloma) - 1)        
		mBeta  =  exp((offmb-v)/slomb)/taumb
		mInf = mAlpha/(mAlpha + mBeta)
		mTau = 1/(mAlpha + mBeta)
		hAlpha =  exp((offha-v)/sloha)/tauha
		hBeta  =  1.0/tauhb/(exp((offhb-v)/slohb)+1)
		hInf = hAlpha/(hAlpha + hBeta)
		hTau = 1/(hAlpha + hBeta)
	UNITSON
}

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