Olfactory Bulb Network (Davison et al 2003)

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Accession:2730
A biologically-detailed model of the mammalian olfactory bulb, incorporating the mitral and granule cells and the dendrodendritic synapses between them. The results of simulation experiments with electrical stimulation agree closely in most details with published experimental data. The model predicts that the time course of dendrodendritic inhibition is dependent on the network connectivity as well as on the intrinsic parameters of the synapses. In response to simulated odor stimulation, strongly activated mitral cells tend to suppress neighboring cells, the mitral cells readily synchronize their firing, and increasing the stimulus intensity increases the degree of synchronization. For more details, see the reference below.
Reference:
1 . Davison AP, Feng J, Brown D (2003) Dendrodendritic inhibition and simulated odor responses in a detailed olfactory bulb network model. J Neurophysiol 90:1921-35 [PubMed]
Citations  Citation Browser
Model Information (Click on a link to find other models with that property)
Model Type: Realistic Network;
Brain Region(s)/Organism: Olfactory bulb;
Cell Type(s): Olfactory bulb main mitral cell; Olfactory bulb main interneuron granule MC cell;
Channel(s): I Na,t; I L high threshold; I A; I K; I K,leak; I M; I K,Ca; I Sodium; I Calcium; I Potassium;
Gap Junctions:
Receptor(s): GabaA; AMPA; NMDA;
Gene(s):
Transmitter(s): Gaba; Glutamate;
Simulation Environment: NEURON;
Model Concept(s): Oscillations; Synchronization; Spatio-temporal Activity Patterns; Olfaction;
Implementer(s): Davison, Andrew [Andrew.Davison at iaf.cnrs-gif.fr];
Search NeuronDB for information about:  Olfactory bulb main mitral cell; Olfactory bulb main interneuron granule MC cell; GabaA; AMPA; NMDA; I Na,t; I L high threshold; I A; I K; I K,leak; I M; I K,Ca; I Sodium; I Calcium; I Potassium; Gaba; Glutamate;
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bulbNet
README *
cadecay.mod *
flushf.mod *
kA.mod *
kca.mod *
kfasttab.mod *
kM.mod *
kslowtab.mod *
lcafixed.mod *
nafast.mod *
nagran.mod *
nmdanet.mod *
bulb.hoc
calcisilag.hoc *
ddi_baseline.gnu *
ddi_baseline.ses *
experiment_ddi_baseline.hoc *
experiment_odour_baseline.hoc *
granule.tem *
init.hoc *
input.hoc *
input1 *
mathslib.hoc *
mitral.tem *
mosinit.hoc *
odour_baseline.connect
odour_baseline.gnu *
odour_baseline.ses *
parameters_ddi_baseline.hoc *
parameters_odour_baseline.hoc *
screenshot.png *
tabchannels.dat *
tabchannels.hoc *
                            
// experiment_ddi_baseline.hoc
// Olfactory bulb network model: experiment file
//   for dendrodendritic inhibition.
// Andrew Davison, The Babraham Institute, 2000.

// *** Set inputs and connections
set_no_input()
glomshock(20,2,5)
randomise_NMDA(NMDAweight,(0.5*NMDAweight)^2)

// *** Voltage clamp mitral cell
mit[3][3].GABAA.e = 0 // mV
objref vclamp
mit[3][3].soma vclamp = new SEClamp(0.5)
vclamp.rs = 2 // Mohm
vclamp.dur1 = 1
vclamp.amp1 = -65
vclamp.dur2 = 4000
vclamp.amp2 = -70
vclamp.dur3 = 0
vclamp.amp3 = -65

// *** Set-up recording
objref igabaa, tvec, vgran, vmit, iclamp
record_step = 0.1
record_vec_size = int(tstop/record_step)+1
igabaa = new Vector(record_vec_size)
tvec = new Vector(record_vec_size)
vgran = new Vector(record_vec_size)
vmit = new Vector(record_vec_size)
iclamp = new Vector(record_vec_size)
record_step = 0.1
igabaa.record(&mit[3][3].GABAA.i,record_step)
tvec.record(&t,record_step)
vgran.record(&gran[0][6].periph.v(0.5),record_step)
vmit.record(&mit[0][0].dend.v(0.5),record_step)
iclamp.record(&vclamp.i,record_step)

// *** Process data and print out results
proc print_results() {
  xopen("calcisilag.hoc")
  print_raster(fileroot)
  print_gran_raster(fileroot)
  print_gran_hist(1,fileroot)
  sprint(filename,"%s.curvs",fileroot)
  outfile.wopen(filename)
  for i = 0, tvec.size()-1 {
    outfile.printf("%8.3g %8.3g %8.3g %8.3g %8.3g \n",tvec.x[i],igabaa.x[i],vmit.x[i],vgran.x[i],iclamp.x[i])
  }
  outfile.close()
  print "Results printed to files"
}

xopen("ddi_baseline.ses")