Distinct current modules shape cellular dynamics in model neurons (Alturki et al 2016)

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Accession:223649
" ... We hypothesized that currents are grouped into distinct modules that shape specific neuronal characteristics or signatures, such as resting potential, sub-threshold oscillations, and spiking waveforms, for several classes of neurons. For such a grouping to occur, the currents within one module should have minimal functional interference with currents belonging to other modules. This condition is satisfied if the gating functions of currents in the same module are grouped together on the voltage axis; in contrast, such functions are segregated along the voltage axis for currents belonging to different modules. We tested this hypothesis using four published example case models and found it to be valid for these classes of neurons. ..."
Reference:
1 . Alturki A, Feng F, Nair A, Guntu V, Nair SS (2016) Distinct current modules shape cellular dynamics in model neurons. Neuroscience 334:309-331 [PubMed]
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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: Hippocampus; Amygdala;
Cell Type(s): Abstract single compartment conductance based cell;
Channel(s):
Gap Junctions:
Receptor(s):
Gene(s):
Transmitter(s):
Simulation Environment: NEURON;
Model Concept(s): Simplified Models; Activity Patterns; Oscillations; Methods; Olfaction;
Implementer(s):
/
AlturkiEtAl2016
2_Pospischil
Original
README.html *
cadecay_destexhe.mod *
HH_traub.mod *
IL_gutnick.mod
IM_cortex.mod
IT_huguenard.mod
demo_IN_FS.hoc *
demo_PY_IB.hoc *
demo_PY_IBR.hoc *
demo_PY_LTS.hoc *
demo_PY_RS.hoc *
fig5b.jpg *
mosinit.hoc *
rundemo.hoc *
sIN_template *
sPY_template *
sPYb_template *
sPYbr_template *
sPYr_template *
                            
TITLE Fast mechanism for submembranal Ca++ concentration (cai)
:
: Takes into account:
:
:	- increase of cai due to calcium currents
:	- extrusion of calcium with a simple first order equation
:
: This mechanism is compatible with the calcium pump "cad" and has the 
: same name and parameters; however the parameters specific to the pump
: are dummy here.
:
: Parameters:
:
:	- depth: depth of the shell just beneath the membran (in um)
:	- cainf: equilibrium concentration of calcium (2e-4 mM)
:	- taur: time constant of calcium extrusion (must be fast)
:	- kt,kd: dummy parameters
:
: Written by Alain Destexhe, Salk Institute, 1995
:

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

NEURON {
	SUFFIX cad
	USEION ca READ ica, cai WRITE cai
	RANGE depth,kt,kd,cainf,taur
}

UNITS {
	(molar) = (1/liter)			: moles do not appear in units
	(mM)	= (millimolar)
	(um)	= (micron)
	(mA)	= (milliamp)
	(msM)	= (ms mM)
}

CONSTANT {
	FARADAY = 96489		(coul)		: moles do not appear in units
:	FARADAY = 96.489	(k-coul)	: moles do not appear in units
}

PARAMETER {
	depth	= .1	(um)		: depth of shell
	taur	= 5	(ms)		: rate of calcium removal
	cainf	= 2e-4	(mM)
	kt	= 0	(mM/ms)		: dummy
	kd	= 0	(mM)		: dummy
}

STATE {
	cai		(mM) 
}

INITIAL {
	cai = cainf
}

ASSIGNED {
	ica		(mA/cm2)
	drive_channel	(mM/ms)
}
	
BREAKPOINT {
	SOLVE state METHOD derivimplicit
}

DERIVATIVE state { 

	drive_channel =  - (10000) * ica / (2 * FARADAY * depth)

	if (drive_channel <= 0.) { drive_channel = 0. }	: cannot pump inward

	cai' = drive_channel + (cainf-cai)/taur
}