Intracortical synaptic potential modulation by presynaptic somatic potential (Shu et al. 2006, 2007)

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Accession:135787
" ... Here we show that the voltage fluctuations associated with dendrosomatic synaptic activity propagate significant distances along the axon, and that modest changes in the somatic membrane potential of the presynaptic neuron modulate the amplitude and duration of axonal action potentials and, through a Ca21- dependent mechanism, the average amplitude of the postsynaptic potential evoked by these spikes. These results indicate that synaptic activity in the dendrite and soma controls not only the pattern of action potentials generated, but also the amplitude of the synaptic potentials that these action potentials initiate in local cortical circuits, resulting in synaptic transmission that is a mixture of triggered and graded (analogue) signals."
Reference:
1 . Shu Y, Duque A, Yu Y, Haider B, McCormick DA (2007) Properties of action-potential initiation in neocortical pyramidal cells: evidence from whole cell axon recordings. J Neurophysiol 97:746-60 [PubMed]
2 . Shu Y, Hasenstaub A, Duque A, Yu Y, McCormick DA (2006) Modulation of intracortical synaptic potentials by presynaptic somatic membrane potential. Nature 441:761-5 [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; Axon;
Brain Region(s)/Organism:
Cell Type(s): Neocortex L5/6 pyramidal GLU cell;
Channel(s): I Na,t; I L high threshold; I A; I K; I M; I h; I K,Ca; I_AHP; I_KD;
Gap Junctions:
Receptor(s): GabaA; AMPA; NMDA;
Gene(s):
Transmitter(s):
Simulation Environment: NEURON;
Model Concept(s): Action Potential Initiation; Detailed Neuronal Models; Action Potentials; Synaptic Integration;
Implementer(s):
Search NeuronDB for information about:  Neocortex L5/6 pyramidal GLU cell; GabaA; AMPA; NMDA; I Na,t; I L high threshold; I A; I K; I M; I h; I K,Ca; I_AHP; I_KD;
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ShuEtAl20062007
readme.txt
ampa5.mod *
ca.mod *
cad.mod
caL3d.mod *
capump.mod
gabaa5.mod *
Gfluct.mod *
ia.mod *
iahp.mod *
iahp2.mod *
ih.mod
im.mod *
kca.mod *
km.mod *
kv.mod *
na.mod *
NMDA_Mg.mod *
nmda5.mod *
release.mod *
2006_Nature.pdf
2006_Nature_supp.pdf
best_full_axon_decay.hoc
best_full_axon_spike_init.hoc
decay_constant.gif
for_decay.m
for_initiation.m
j4a.hoc *
j4a_removedendrite.hoc
j4a_removedendrite1.hoc
j7.hoc *
j8.hoc *
j8_removedendrite.hoc
lcAS3.hoc *
mosinit.hoc
spike_initiation.gif
                            
TITLE Fluctuating conductances

COMMENT
-----------------------------------------------------------------------------

	Fluctuating conductance model for synaptic bombardment
	======================================================

THEORY

  Synaptic bombardment is represented by a stochastic model containing
  two fluctuating conductances g_e(t) and g_i(t) descibed by:

     Isyn = g_e(t) * [V - E_e] + g_i(t) * [V - E_i]
     d g_e / dt = -(g_e - g_e0) / tau_e + sqrt(D_e) * Ft
     d g_i / dt = -(g_i - g_i0) / tau_i + sqrt(D_i) * Ft

  where E_e, E_i are the reversal potentials, g_e0, g_i0 are the average
  conductances, tau_e, tau_i are time constants, D_e, D_i are noise diffusion
  coefficients and Ft is a gaussian white noise of unit standard deviation.

  g_e and g_i are described by an Ornstein-Uhlenbeck (OU) stochastic process
  where tau_e and tau_i represent the "correlation" (if tau_e and tau_i are 
  zero, g_e and g_i are white noise).  The estimation of OU parameters can
  be made from the power spectrum:

     S(w) =  2 * D * tau^2 / (1 + w^2 * tau^2)

  and the diffusion coeffient D is estimated from the variance:

     D = 2 * sigma^2 / tau


NUMERICAL RESOLUTION

  The numerical scheme for integration of OU processes takes advantage 
  of the fact that these processes are gaussian, which led to an exact
  update rule independent of the time step dt (see Gillespie DT, Am J Phys 
  64: 225, 1996):

     x(t+dt) = x(t) * exp(-dt/tau) + A * N(0,1)

  where A = sqrt( D*tau/2 * (1-exp(-2*dt/tau)) ) and N(0,1) is a normal
  random number (avg=0, sigma=1)


IMPLEMENTATION

  This mechanism is implemented as a nonspecific current defined as a
  point process.


PARAMETERS

  The mechanism takes the following parameters:

     E_e = 0  (mV)		: reversal potential of excitatory conductance
     E_i = -75 (mV)		: reversal potential of inhibitory conductance

     g_e0 = 0.0121 (umho)	: average excitatory conductance
     g_i0 = 0.0573 (umho)	: average inhibitory conductance

     std_e = 0.0030 (umho)	: standard dev of excitatory conductance
     std_i = 0.0066 (umho)	: standard dev of inhibitory conductance

     tau_e = 2.728 (ms)		: time constant of excitatory conductance
     tau_i = 10.49 (ms)		: time constant of inhibitory conductance


Gfluct2: conductance cannot be negative


REFERENCE

  Destexhe, A., Rudolph, M., Fellous, J-M. and Sejnowski, T.J.  
  Fluctuating synaptic conductances recreate in-vivo--like activity in
  neocortical neurons. Neuroscience 107: 13-24 (2001).

  (electronic copy available at http://cns.iaf.cnrs-gif.fr)


  A. Destexhe, 1999

-----------------------------------------------------------------------------
ENDCOMMENT



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

NEURON {
	POINT_PROCESS Gfluct2
	RANGE g_e, g_i, E_e, E_i, g_e0, g_i0, g_e1, g_i1
	RANGE std_e, std_i, tau_e, tau_i, D_e, D_i
	RANGE new_seed
	NONSPECIFIC_CURRENT i
}

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

PARAMETER {
	dt		(ms)

	E_e	= 0 	(mV)	: reversal potential of excitatory conductance
	E_i	= -75 	(mV)	: reversal potential of inhibitory conductance

	g_e0	= 0.0121 (umho)	: average excitatory conductance
	g_i0	= 0.0573 (umho)	: average inhibitory conductance

	std_e	= 0.0030 (umho)	: standard dev of excitatory conductance
	std_i	= 0.0066 (umho)	: standard dev of inhibitory conductance

	tau_e	= 2.728	(ms)	: time constant of excitatory conductance
	tau_i	= 10.49	(ms)	: time constant of inhibitory conductance
}

ASSIGNED {
	v	(mV)		: membrane voltage
	i 	(nA)		: fluctuating current
	g_e	(umho)		: total excitatory conductance
	g_i	(umho)		: total inhibitory conductance
	g_e1	(umho)		: fluctuating excitatory conductance
	g_i1	(umho)		: fluctuating inhibitory conductance
	D_e	(umho umho /ms) : excitatory diffusion coefficient
	D_i	(umho umho /ms) : inhibitory diffusion coefficient
	exp_e
	exp_i
	amp_e	(umho)
	amp_i	(umho)
}

INITIAL {
	g_e1 = 0
	g_i1 = 0
	if(tau_e != 0) {
		D_e = 2 * std_e * std_e / tau_e
		exp_e = exp(-dt/tau_e)
		amp_e = std_e * sqrt( (1-exp(-2*dt/tau_e)) )
	}
	if(tau_i != 0) {
		D_i = 2 * std_i * std_i / tau_i
		exp_i = exp(-dt/tau_i)
		amp_i = std_i * sqrt( (1-exp(-2*dt/tau_i)) )
	}
}

BREAKPOINT {
	SOLVE oup
	if(tau_e==0) {
	   g_e = std_e * normrand(0,1)
	}
	if(tau_i==0) {
	   g_i = std_i * normrand(0,1)
	}
	g_e = g_e0 + g_e1
	if(g_e < 0) { g_e = 0 }
	g_i = g_i0 + g_i1
	if(g_i < 0) { g_i = 0 }
	i = g_e * (v - E_e) + g_i * (v - E_i)
}


PROCEDURE oup() {		: use Scop function normrand(mean, std_dev)
   if(tau_e!=0) {
	g_e1 =  exp_e * g_e1 + amp_e * normrand(0,1)
   }
   if(tau_i!=0) {
	g_i1 =  exp_i * g_i1 + amp_i * normrand(0,1)
   }
}