Afferent Integration in the NAcb MSP Cell (Wolf et al. 2005)

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Accession:112834
"We describe a computational model of the principal cell in the nucleus accumbens (NAcb), the medium spiny projection (MSP) neuron. The model neuron, constructed in NEURON, includes all of the known ionic currents in these cells and receives synaptic input from simulated spike trains via NMDA, AMPA, and GABAA receptors. ... results suggest that afferent information integration by the NAcb MSP cell may be compromised by pathology in which the NMDA current is altered or modulated, as has been proposed in both schizophrenia and addiction."
Reference:
1 . Wolf JA, Moyer JT, Lazarewicz MT, Contreras D, Benoit-Marand M, O'Donnell P, Finkel LH (2005) NMDA/AMPA ratio impacts state transitions and entrainment to oscillations in a computational model of the nucleus accumbens medium spiny projection neuron. J Neurosci 25:9080-95 [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): Nucleus accumbens spiny projection neuron;
Channel(s): I Na,p; I Na,t; I L high threshold; I N; I T low threshold; I A; I h; I K,Ca; I Krp; I R; I Q;
Gap Junctions:
Receptor(s): GabaA; AMPA; NMDA;
Gene(s):
Transmitter(s):
Simulation Environment: NEURON;
Model Concept(s): Oscillations; Schizophrenia; Addiction;
Implementer(s): Wolf, John A. [johnwolf at warpmail.net]; Moyer, Jason [jtmoyer at seas.upenn.edu];
Search NeuronDB for information about:  GabaA; AMPA; NMDA; I Na,p; I Na,t; I L high threshold; I N; I T low threshold; I A; I h; I K,Ca; I Krp; I R; I Q;
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nacb_msp
tau_tables
readme.html
AMPA.mod
bkkca.mod *
cadyn.mod *
caL.mod *
caL13.mod *
caldyn.mod
can.mod *
caq.mod *
car.mod *
cat.mod *
GABA.mod *
kaf.mod *
kas.mod *
kir.mod *
krp.mod *
naf.mod *
nap.mod *
NMDA.mod
skkca.mod *
stim.mod *
_run_me.hoc
all_tau_vecs.hoc *
baseline_values.txt *
basic_procs.hoc
create_mspcells.hoc *
current_clamp.ses *
make_netstims.hoc
mosinit.hoc *
msp_template.hoc
nacb_main.hoc
netstims_template.hoc *
screenshot.jpg
screenshot2.jpg
stimxout_jns_sqwave.dat
synapse_templates.hoc
                            
TITLE    AMPA synapse for nucleus accumbens model
: see comments below

NEURON {
	POINT_PROCESS AMPA
	RANGE gbar, tau_r, tau_d, scale, spkcnt, countflag, i, t1, ca_ratio, ical, itmp, qfact
	NONSPECIFIC_CURRENT i
 	USEION cal WRITE ical VALENCE 2

}

UNITS {
	(nA) = (nanoamp)
	(mV) = (millivolt)
	(umho) = (micromho)
}

PARAMETER {
	gbar = 8.5e-4   (umho) 	: approx 0.5:1 NMDA:AMPA ratio (Myme 2003)
							:   with mg = 0, vh = -70, one pulse, NMDA = 300 pS
							:   here AMPA = 593 pS (NMDA set to Dalby 2003)
	tau_r = 2.2 	(ms)   	: Gotz 1997, Table 1 - rise tau
	tau_d = 11.5  	(ms)   	: Gotz 1997, Table 1 - decay tau
	
	Erev = 0    	(mV)   	: reversal potential, Jahn 1998
	saturate = 1.2 			: causes the conductance to saturate - matched to 
							:    Destexhe's reduced model in [1]
	qfact = 2				: convert 22 degC to 35 degC
	ca_ratio = 0.005			: ratio of calcium current to total current
}							: Burnashev/Sakmann J Phys 1995 485:403-418
							: with Carter/Sabatini Neuron 2004 44:483-493


ASSIGNED {
	g (umho)
	v (mV)   		: postsynaptic voltage
	itmp	(nA)	: temp value of current
	i (nA)   		: nonspecific current = g*(v - Erev)
	ical (nA)		: calcium current through AMPA synapse (Carter/Sabatini)
	t1 (ms)
	
	y1_add (/ms)    : value added to y1 when a presynaptic spike is registered
	y1_loc (/ms)

	countflag		: start/stop counting spikes delivered
	spkcnt			: counts number of events delivered to synapse
	scale			: scale allows the current to be scaled by weight
}					: so NetCon(...,2) gives 2*the current as NetCon(...,1)


STATE { 
	y1 (/ms) 
	y2    			: sum of beta-functions, describing the total conductance
}

INITIAL {
  	y1_add = 0
	scale = 0
	spkcnt = 0
	countflag = 0
	t1 = 0
	y1_loc = 0
}

BREAKPOINT {
  	SOLVE betadyn METHOD cnexp
	g = gbar * y2
  	itmp = scale * g * (v - Erev)
  	i = (1-ca_ratio) * itmp
  	ical = ca_ratio * itmp
}

DERIVATIVE betadyn {
	: dynamics of the beta-function, from [2]
	y1' = -y1 / (tau_d/qfact)
	y2' = y1 - y2 / (tau_r/qfact)
}

NET_RECEIVE( weight, y1_loc (/ms) ) {
	: updating the local y1 variable
	y1_loc = y1_loc*exp( -(t - t1) / (tau_d/qfact) )

	: y1_add is dependent on the present value of the local
	: y1 variable, y1_loc
	y1_add = (1 - y1_loc/saturate)

	: update the local y1 variable
	y1_loc = y1_loc + y1_add

	: presynaptic spike is finaly registered
	y1 = y1 + y1_add

	: store the spike time
	t1 = t

	spkcnt = spkcnt + 1

	scale = weight
}


COMMENT
Author Johan Hake (c) spring 2004
:     Summate input from many presynaptic sources and saturate 
:     each one of them during heavy presynaptic firing

: [1] Destexhe, A., Z. F. Mainen and T. J. Sejnowski (1998)
:     Kinetic models of synaptic transmission
:     In C. Koch and I. Segev (Eds.), Methods in Neuronal Modeling

: [2] Rotter, S. and M. Diesmann (1999) Biol. Cybern. 81, 381-402
:     Exact digital simulation of time-invariant linear systems with application 
:     to neural modeling



Dalby, N. O., and Mody, I. (2003). Activation of NMDA receptors in rat
dentate gyrus granule cells by spontaneous and evoked transmitter
release. J Neurophysiol 90, 786-797.

Gotz, T., Kraushaar, U., Geiger, J., Lubke, J., Berger, T., and Jonas,
P. (1997). Functional properties of AMPA and NMDA receptors expressed in
identified types of basal ganglia neurons. J Neurosci 17, 204-215.

Jahn K, Bufler J, Franke C (1998) Kinetics of AMPA-type glutamate
receptor channels in rat caudate-putamen neurones show a wide range of
desensitization but distinct recovery characteristics. Eur J Neurosci
10:664-672.

Myme, C. I., Sugino, K., Turrigiano, G. G., and Nelson, S. B. (2003).
The NMDA-to-AMPA ratio at synapses onto layer 2/3 pyramidal neurons is
conserved across prefrontal and visual cortices. J Neurophysiol 90,
771-779.

Gutfreund H, Kinetics for the Life Sciences, Cambridge University Press,
1995, pg 234.  (suggested by Ted Carnevale)
ENDCOMMENT


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