Electrotonic transform and EPSCs for WT and Q175+/- spiny projection neurons (Goodliffe et al 2018)

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Accession:236310
This model achieves electrotonic transform and computes mean inward and outward attenuation from 0 to 500 Hz input; and randomly activates synapses along dendrites to simulate AMPAR mediated EPSCs. For electrotonic analysis, in Elec folder, the entry file is MSNelec_transform.hoc. For EPSC simulation, in Syn folder, the entry file is randomepsc.hoc. Run read_EPSCsims_mdb_alone.m next with the simulated parameter values specified to compute the mean EPSC.
Reference:
1 . Goodliffe JW, Song H, Rubakovic A, Chang W, Medalla M, Weaver CM, Luebke JI (2018) Differential changes to D1 and D2 medium spiny neurons in the 12-month-old Q175+/- mouse model of Huntington's Disease. PLoS One 13:e0200626 [PubMed]
Model Information (Click on a link to find other models with that property)
Model Type: Synapse;
Brain Region(s)/Organism: Striatum;
Cell Type(s): Neostriatum spiny neuron;
Channel(s):
Gap Junctions:
Receptor(s): AMPA;
Gene(s):
Transmitter(s):
Simulation Environment: NEURON;
Model Concept(s): Detailed Neuronal Models; Membrane Properties; Electrotonus; Synaptic-input statistic; Huntington's;
Implementer(s):
Search NeuronDB for information about:  AMPA;
/
GoodliffeEtAl2018
Syn
tau_tables
bkkca.mod
cadyn.mod *
caL.mod
caL13.mod
caldyn.mod
can.mod
caq.mod *
car.mod
cat.mod
kaf.mod
kas.mod
kdr.mod
kir.mod *
krp.mod *
linearIclamp.mod
naf.mod
nap.mod
skkca.mod
stim.mod *
actionPotentialPlayer.hoc *
all_tau_vecs.hoc
analyticFunctions.hoc *
analyze_EPSC.m
aux_procs.hoc
baseline_values.txt
basic_procs.hoc
createFit_WTD1.m
electro_procs.hoc
fixnseg.hoc *
load_scripts.hoc
msp_template.hoc
PFC-V1_AddSynapses.hoc
PFC-V1_AddSynapses_fix.hoc
PFC-V1_AddSynapses_neg.hoc
PFC-V1_AddSynapses_negexp.hoc
plot_seClamp_i.ses
ran_test.hoc
randomepsc.hoc
ranstream.hoc
read_EPSCsims_mdb_alone.m
readcell.hoc
readNRNbin_Vclamp.m
                            
//****************************************************************************
// basic_procs.hoc defines procedures for setting conductances and range
// variables of channels - these are primarily used to change variables
// from the gui

proc set_pas() {NEW_GPAS = $1
    forall if (ismembrane("pas")) {
        Ra      = RA
        Cm      = CM
        g_pas   = 0.0001437349
        e_pas   = -79.2586192087
    }
    forsec "axon_myelin" { cm = CM * CM_MYELINFAC }
}

proc set_naf() {		NEW_GBAR = $1
	nG_NAF = NEW_GBAR
	forall if (ismembrane("naf")) {gnabar_naf = G_NAF_AIS}
	forsec "soma" {gnabar_naf = nG_NAF}
	forsec proximal {gnabar_naf = nG_NAF*0.273/9}
	forsec middend {gnabar_naf = nG_NAF*0.273/9}
	forsec distal {gnabar_naf = nG_NAF*0.0975/9}
	
}

proc set_nap() {		NEW_GBAR = $1
	nG_NAP = NEW_GBAR
	forsec "soma" {gnabar_nap = nG_NAP}
	forsec "dend" {gnabar_nap = nG_NAP*0.013802/4}
}

proc set_shifts() {
	forall if (ismembrane("naf")) {
		mshift_naf = mshift_na
		hshift_naf = hshift_na
	}
	forall if (ismembrane("nap")) {
		mshift_nap = mshift_na
		hshift_nap = hshift_na
	}
	forall if (ismembrane("kas")) {
		mshift_kas = mshift_ka
		hshift_kas = hshift_ka
		htaushift_kas = HTAUSHIFT_KAS - mshift_ka
	}
	forall if (ismembrane("kaf")) {
		mshift_kaf = mshift_ka
		hshift_kaf = hshift_ka
	}
	forall if (ismembrane("kdr")) {
		ashift_kdr = ashift_k
		bshift_kdr = bshift_k
	}
	forall if (ismembrane("naf")) {
		mshift_naf = mshift_na
		hshift_naf = hshift_na
	}
	forall if (ismembrane("bkkca")) {
		m1half_bkkca = M1HALF_BK - mshift_ka
	    m2half_bkkca = M2HALF_BK - mshift_ka
	    m3half_bkkca = M3HALF_BK - mshift_ka
	    m4half_bkkca = M4HALF_BK - mshift_ka
	}
	forall if (ismembrane("caL")) {
		mshift_caL = mshift_ca
	    hshift_caL = hshift_ca
	    mshift_caL13 = mshift_ca
	    hshift_caL13 = hshift_ca
	    mshift_can = mshift_ca
	    hshift_can = hshift_ca
	    mshift_car = mshift_ca
	    hshift_car = hshift_ca
	    mshift_cat = mshift_ca
	    hshift_cat = hshift_ca
	}
}

/************************************************
proc set_nafa() {		NEW_GBAR = $1
	nG_NAF_AIS = NEW_GBAR
	forsec "axon[0]" {gnabar_naf = nG_NAF_AIS 
		mslope_naf = SOMA_MSLOPE_NAF * AXON_MSLOPEFAC
        mshift_naf = mshift_na - AXON_MSHIFT
        hshift_naf = hshift_na - AXON_HSHIFT}
    forsec "axon[1]" {gnabar_naf = nG_NAF_AIS 
		mslope_naf = SOMA_MSLOPE_NAF * AXON_MSLOPEFAC
        mshift_naf = mshift_na - AXON_MSHIFT
        hshift_naf = hshift_na - AXON_HSHIFT}
    
}

proc set_napa() {		NEW_GBAR = $1
	nG_NAP_AIS = NEW_GBAR
	forsec "axon[0]" {gnabar_nap = 4e-05}
	forsec "axon[1]" {gnabar_nap = 4e-05}
}

proc set_kafa() {		NEW_GBAR = $1
	nG_KAF_AIS = NEW_GBAR
	forsec "axon[0]" {gkbar_kaf = nG_KAF_AIS mshift_kaf = 0}
	forsec "axon[1]" {gkbar_kaf = nG_KAF_AIS hshift_kaf = 0}
}

proc set_kasa() {		NEW_GBAR = $1
	nG_KAS_AIS = NEW_GBAR
	forsec "axon[0]" {gkbar_kas = nG_KAS_AIS}
	forsec "axon[1]" {gkbar_kas = nG_KAS_AIS}
}

proc set_kdra() {		NEW_GBAR = $1
	nG_KDR_AIS = NEW_GBAR
	forsec "axon[0]" {gkbar_kdr = nG_KDR_AIS}
	forsec "axon[1]" {gkbar_kdr = nG_KDR_AIS}
}

***********************************************/

proc set_ek() {	newEK = $1
	forsec "MSP" {ek = newEK}
	EK = newEK
}

proc set_kir() {		NEW_GBAR = $1
	nG_KIR = NEW_GBAR
	forall if (ismembrane("kir")) {gkbar_kir = G_KIR
	qfact_kir = 0.36 
	mshift_kir = 105.8433503124
	mslope_kir = 14.9975692214
	}
}

proc set_kas() {		NEW_GBAR = $1
	nG_KAS = NEW_GBAR
	forsec "soma" {gkbar_kas = nG_KAS}
	forsec middend {gkbar_kas = nG_KAS*0.3893/3.601}
	forsec distal {gkbar_kas = nG_KAS*0.3893/3.601}
}

proc set_kaf() {		NEW_GBAR = $1
	nG_KAF = NEW_GBAR
	forsec "soma" {gkbar_kaf = nG_KAF}
	
	forsec proximal {gkbar_kaf = nG_KAF}
	
	forsec middend {gkbar_kaf = nG_KAF*0.016821/0.076524}
	

	
	forsec distal {gkbar_kaf = nG_KAF*0.011214/0.076524}

}

proc set_kdr() {		NEW_GBAR = $1
	nG_KDR = NEW_GBAR
	forsec "soma" {gkbar_kdr = nG_KDR}
	forsec "dend"  {gkbar_kdr = nG_KDR}
}

proc set_bkkca() {		NEW_GBAR = $1
	nG_BKKCA = NEW_GBAR
	forall if(ismembrane("bkkca")) {gkbar_bkkca = NEW_GBAR}
}

proc set_skkca() {		NEW_GBAR = $1
	nG_SKKCA = NEW_GBAR
	forall if(ismembrane("skkca")) {gkbar_skkca = NEW_GBAR}
}


proc set_caL() {		NEW_PBAR = $1
	nP_CAL = NEW_PBAR
	forall if (ismembrane("caL")) {pbar_caL = NEW_PBAR}
}

proc set_caL13() {		NEW_PBAR = $1
	nP_CAL13 = NEW_PBAR
	forall if (ismembrane("caL13")) {pcaLbar_caL13 = NEW_PBAR}
}

proc set_can() {		NEW_PBAR = $1
	nP_CAN = NEW_PBAR
	forall if (ismembrane("can")) {pbar_can = NEW_PBAR}
}

proc set_car() {		NEW_PBAR = $1
	nP_CAR = NEW_PBAR
	forall if (ismembrane("car")) {pcarbar_car = NEW_PBAR}
}

proc set_caq() {		NEW_PBAR = $1
	nP_CAQ = NEW_PBAR
	forall if (ismembrane("caq")) {pcarbar_caq = NEW_PBAR}
}

proc set_cat() {		NEW_PBAR = $1
	nP_CAT = NEW_PBAR
	forall if (ismembrane("cat")) {pcatbar_cat = NEW_PBAR}
}

//******************
// Calcium dynamics procs

proc set_cainf() {	NEW_CAINF = $1
	nCA_INF = NEW_CAINF
	forall if (ismembrane("cadyn")) {cainf_cadyn = CAINF}
	forall if (ismembrane("caldyn")) {cainf_caldyn = CAINF}
}

proc set_taur() {	NEW_TAUR = $1
	nCA_TAUR = NEW_TAUR
	forall if (ismembrane("cadyn")) {taur_cadyn = TAUR}
	forall if (ismembrane("caldyn")) {taur_caldyn = TAUR}
}
proc set_cadrive() { 	NEW_DRIVE = $1
	nCA_DRIVE = NEW_DRIVE
	forall if (ismembrane("cadyn")) {drive_cadyn = CA_DRIVE}
	forall if (ismembrane("caldyn")) {drive_caldyn = CA_DRIVE}
}
proc set_pump() {	NEW_PUMP = $1
	nCA_PUMP = NEW_PUMP
	forall if (ismembrane("cadyn")) {pump_cadyn = CA_PUMP}
	forall if (ismembrane("caldyn")) {pump_caldyn = CA_PUMP}
}
//******************

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