CA3 Network Model of Epileptic Activity (Sanjay et. al, 2015)

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Accession:186768
This computational study investigates how a CA3 neuronal network consisting of pyramidal cells, basket cells and OLM interneurons becomes epileptic when dendritic inhibition to pyramidal cells is impaired due to the dysfunction of OLM interneurons. After standardizing the baseline activity (theta-modulated gamma oscillations), systematic changes are made in the connectivities between the neurons, as a result of step-wise impairment of dendritic inhibition.
Reference:
1 . Sanjay M, Neymotin SA, Krothapalli SB (2015) Impaired dendritic inhibition leads to epileptic activity in a computer model of CA3. Hippocampus 25:1336-50 [PubMed]
Citations  Citation Browser
Model Information (Click on a link to find other models with that property)
Model Type: Realistic Network; Extracellular;
Brain Region(s)/Organism:
Cell Type(s): Hippocampus CA3 pyramidal GLU cell; Hippocampus CA3 interneuron basket GABA cell; Hippocampus CA3 stratum oriens lacunosum-moleculare interneuron;
Channel(s):
Gap Junctions:
Receptor(s): GabaA; AMPA; NMDA;
Gene(s): HCN1; HCN2;
Transmitter(s):
Simulation Environment: NEURON; Python;
Model Concept(s): Activity Patterns; Oscillations; Pathophysiology; Epilepsy; Brain Rhythms;
Implementer(s): Neymotin, Sam [Samuel.Neymotin at nki.rfmh.org]; Sanjay, M [msanjaycmc at gmail.com];
Search NeuronDB for information about:  Hippocampus CA3 pyramidal GLU cell; Hippocampus CA3 interneuron basket GABA cell; GabaA; AMPA; NMDA;
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SanjayEtAl2015
readme.html
CA1ih.mod *
CA1ika.mod *
CA1ikdr.mod *
CA1ina.mod *
caolmw.mod *
capr.mod *
icaolmw.mod *
icapr.mod *
iholmkop.mod *
iholmw.mod *
ihpyrkop.mod *
kahppr.mod *
kaolmkop.mod *
kapyrkop.mod *
kcaolmw.mod *
kcpr.mod *
kdrbwb.mod *
kdrolmkop.mod *
kdrpr.mod *
kdrpyrkop.mod *
misc.mod *
MyExp2Syn.mod *
MyExp2SynAlpha.mod *
MyExp2SynBB.mod *
MyExp2SynNMDA.mod *
MyExp2SynNMDABB.mod *
nafbwb.mod *
nafolmkop.mod *
nafpr.mod *
nafpyrkop.mod *
stats.mod
vecst.mod *
wrap.mod *
aux_fun.inc *
declist.hoc *
decmat.hoc *
decnqs.hoc *
decvec.hoc *
default.hoc *
drline.hoc *
Epileptic Activity.png
geom.hoc *
geom.py *
grvec.hoc *
init.hoc *
labels.hoc *
local.hoc *
misc.h *
mosinit.py
network.py *
networkmsj.py
nqs.hoc *
nqs_utils.hoc *
nrnoc.hoc *
params.py
pyinit.py *
run.py
simctrl.hoc *
stats.hoc *
syncode.hoc *
xgetargs.hoc *
xtmp
                            
// $Id: labels.hoc,v 1.95 2011/01/14 16:46:02 billl Exp $

load_file("declist.hoc")
// keep track of version number for future changes
// eg if (label_hoc_vers>88) rcsopen("labels.hoc",88) // go back to 88
labels_hoc_vers=find_num("$Id: labels.hoc,v 1.95 2011/01/14 16:46:02 billl Exp $","1\\."," ")
objref NCv,CODEv,DELv
objref PRIDv,POIDv,PRv,POv,DISTv,WT0v,WT1v // mo(1) will assign these
declare("ce",nil,"CTYP",new List(),"CPLA",new List(),"TPA",new List(),"nm",new List())
declare("STYP",new List(),"ncells",0,"ZTYP",new List(),"INCOL",new List())
declare("DEND",0,"SOMA",1,"AXON",2) // compartment codes - only 3 for now

//* utility functions
// plmin(val,var)
func plmin() { return $1 + $2*(2*u_rand() - 1) } 

//* cell types: 
// iex(), returns numeric index associated with a string or string object
func iex () { 
  if (argtype(1)==2) sprint(tstr,"x=%s",$s1) else sprint(tstr,"x=%s",$o1.s)
  execute(tstr) return x 
}
// ice(), returns whether cell is an inhib cell based on its name starting with I
func ice () { local x
  if (argtype(1)==2) return strm($s1,"^I")
  if (argtype(1)==0) x=$1 else if (argtype(1)==1) x=$o1.type 
  return strm(CTYP.o(x).s,"^I")
}
//* GetLyr - return layer of type
func GetLyr () { local x localobj st
  st=new String()
  if (argtype(1)==2) st.s=$s1 else if (argtype(1)==0) st.s=CTYP.o($1).s else {
    st.s=CTYP.o($o1.type).s }
  sscanf(st.s,"%*1s%d",&x)
  return x
}

proc printtype () { local i
  for (i=1;argtype(i)==0;i+=1) if ($i!=-1) printf("%s(%d) ",CTYP.o($i).s,$i)
  if (argtype(i)==2) printf("%s",$si) else print ""
}
proc celltype () { localobj st
  st=new String("\n")
  if (argtype(2)==2) st.s=$s2
  if (argtype(1)==0) printtype(ce.o($1).type,st.s) else printtype($o1.type,st.s) 
}

obfunc names2indices () { local x localobj lo,xo,st
  lo=new List() st=new String()
  split($s1,lo)
  for ltr(xo,lo,&x) { sprint(st.s,"%s=%d",xo.s,x) execute(st.s) }
  return lo
}

// at some point may want to divide up this list into cell type -- eg RS,IB and location
CTYP=names2indices("NU,SM,DP,SU,IN,TC,IRE,ITH,E6,I6,I6C,I6L,E5B,E5R,I5,I5L,E4,I4,I4L,E2,E2B,I2,I2Q,I2C,I2L,RS,IB,LTS,FS,ECA1,ICA1,ICA1L,EDG,IDG,IDGL,ECA3,ICA3,ICA3L,E3,I3,I3L")
CTYPi=CTYP.count  // number of cell types

// 1 cmp nrn, 2 cmp nrn, multi cmp nrn, intfire1, INTF, invlfire, nstim
for scase2(XO,"1-CMP","CMP1","2-CMP","CMP2","MULTI-CMP","MC","IntFire1","IF1","INTF","IF",\
          "INVLF","IFV","NStim","STM") { CPLA.append(XO)
  sprint(tstr,"%s=%d",XO.t,i1) execute(tstr) }
CPLAi=CPLA.count // count of cell templates

for scase2(XO,"REAL","RL","ARTC","AC","SOMA","SO","DEND","DN") {TPA.append(XO)}
TPAi=TPA.count

proc ae () { localobj xo
  STYP.remove_all
  for scase2(xo,"AMPA","AM","NMDA","NM","GABAA","GA","GABAB","GB",\
             "AMPA2","AM2","NMDA2","NM2","GABAA2","GA2","GABAB2","GB2",\
           "IClamp","IC","AMPA/NMDA","EX","GABAA/GABAB2","IX","Exp2Syn","E2Sy"){
    STYP.append(new String2(xo.t,xo.s)) // switch them around here
    sprint(tstr,"%s=%d",xo.t,i1)
    execute(tstr)
  }
  STYPi=STYP.count  // number of cell types
}
ae()

for scase(XO,"DG","CA3","CA1","SUB","PSUB","MEC","LEC") {
  sprint(tstr,"%s=%d",XO.s,i1) execute(tstr) ZTYP.append(new String(XO.s))
}

for scase2(XO,"RIGHT","RIT","INCOL","INC","LEFT","LFT") { INCOL.append(new String(XO.s))
  sprint(tstr,"%s=%d",XO.t,i1) execute(tstr) }
INCOLi=INCOL.count

//* IsLTS - return if type is LTS
func IsLTS () {
  return $1 == I2L || $1 == I4L || $1 == I5L || $1 == I6L 
}
//* IsBurst - return if type is intrinsically bursting
func IsBurst () {
  return $1 == E2B || $1 == E5B
}
//* IsFRB - return true if type is fast regular bursting
func IsFRB () {
  return $1 == E2B
}
//* IsRS - return true if type is regular spiking E cell
func IsRS () {
  return $1 == E2 || $1 == E4 || $1 == E5R || $1 == E6
}
//* IsFS - return true if type is fast spiking interneuron
func IsFS () {
  return $1 == I2 || $1 == I4 || $1 == I5 || $1 == I6 || $1 == ICA3 || $1 == IDG || $1 == ICA1
}

func isartcell () { return sfunc.is_point_process($o1) }