// FILE IN USE 10/12/2004 -- present
/*
Script to add synapses to GP model but not add channel clusters. Clusters
are handled separately by the read_clusters.g file. Clusters are added to
the compartments listed in {clusterfname}, while STN synapses are added to the
compartments listed in {STNfilename}. GP$1_defaults has these two set to the same,
so the default is to have clusters at all STN synapse locations. Users can
overwrite either or both file names to change the locations of syns & clusters.
STN synapse amplitudes are scaled according to the values in {STN_scale}
*/
//The 2000 used below is only to keep the random numbers for STN and striatum different.
if ({snapgate} == 0)
if ({synBack_synch}==0)
randseed {({rseed_STN_postsnap}+{spikeIdx}+2000)}
echo
echo post snapshot random seed is {({rseed_STN_postsnap}+{spikeIdx}+2000)}
echo
end
else
randseed {rseed_STN}
echo
echo snapshot random seed is {rseed_STN}
echo
end
int i, num
float d,l,surf, scalefac, totscale, meanscale
str stncompartment
//create input element tree outside of the cell path
if (!{exists /inputs})
create neutral /inputs
end
create neutral /inputs/STN
num_STN = 0
int num_compart = 0
// Get mean value of scale factors
openfile {STN_scale} r
scalefac = {readfile {STN_scale}}
totscale = 0
num = 0
while (! {eof {STN_scale}})
totscale = {totscale} + {scalefac}
num = {num} + 1
num_compart = {num_compart} + 1
scalefac = {readfile {STN_scale}}
// echo "num is: " {num}
end
closefile {STN_scale}
meanscale = {totscale} / {num}
echo "totscale: " {totscale}
echo "num: " {num}
echo "meanscale: " {meanscale}
echo "num_compart: " {num_compart}
//clear and open file to list compartment names of all excitatory synapses
// File MUST NOT have any blank lines at the end, or function will fail.
echo
echo STNfilename is {STNfilename}
echo
openfile {STNfilename} r
stncompartment = {readfile {STNfilename}}
openfile {STN_scale} r
scalefac = {readfile {STN_scale}}
//cycle through STN input compartments
while (! {eof {STNfilename}})
num_STN = {num_STN} + 1
//Add AMPA synapses
copy /library/AMPA {cellpath}/{stncompartment}/AMPA
addmsg {cellpath}/{stncompartment}/AMPA \
{cellpath}/{stncompartment} CHANNEL Gk Ek
addmsg {cellpath}/{stncompartment} \
{cellpath}/{stncompartment}/AMPA VOLTAGE Vm
// echo "num_STN is " {num_STN}
//get compartment parameters
d = {getfield {cellpath}/{stncompartment} dia}
l = {getfield {cellpath}/{stncompartment} len}
surf = {d}*{l}*{PI}
// scale synapse amplitude
//echo
setfield {cellpath}/{stncompartment}/AMPA gmax {{G_AMPA}*{scalefac}/{meanscale}}
//echo before {getfield {cellpath}/{stncompartment}/AMPA gmax}
setfield {cellpath}/{stncompartment}/AMPA gmax {{{G_AMPA}*{scalefac}/{meanscale}}*{syngain}}
//echo after {getfield {cellpath}/{stncompartment}/AMPA gmax}
//echo
// echo "synapse " {stncompartment} ": " {getfield {cellpath}/{stncompartment}/AMPA gmax}
//set up timetables
create neutral /inputs/STN/{stncompartment}
create timetable /inputs/STN/{stncompartment}/timetable
if ({STN_rate} > 0)
setfield /inputs/STN/{stncompartment}/timetable \
maxtime 20 act_val 1.0 method 2 \
meth_desc1 {1/{STN_rate}} meth_desc2 0.005 meth_desc3 3
call /inputs/STN/{stncompartment}/timetable TABFILL
end
//set up spikegen
create spikegen /inputs/STN/{stncompartment}/spikegen
setfield /inputs/STN/{stncompartment}/spikegen \
output_amp 1 thresh 0.5
//connect timetables to AMPA synapses
if ({STN_rate} > 0)
addmsg /inputs/STN/{stncompartment}/timetable \
/inputs/STN/{stncompartment}/spikegen INPUT activation
addmsg /inputs/STN/{stncompartment}/spikegen \
{cellpath}/{stncompartment}/AMPA SPIKE
end
// get next compartment name
stncompartment = {readfile {STNfilename}}
scalefac = {readfile {STN_scale}}
if ({eof {STN_scale}})
echo "eof scale"
end
end
closefile {STNfilename}
closefile {STN_scale}
if ({num_STN} != {num})
echo "ERROR: number of scale factors doesn't match number of synapses."
quit
end
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