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148 lines
3.2 KiB
148 lines
3.2 KiB
2 years ago
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TITLE detailed model of Glycine receptors
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COMMENT
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-----------------------------------------------------------------------------
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Kinetic model of Glycine-A receptors
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====================================
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C -- C1 -- C2
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O1 O2
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-----------------------------------------------------------------------------
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This mod file does not include mechanisms for the release and time course
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of transmitter; it is to be used in conjunction with a sepearate mechanism
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to describe the release of transmitter and that provides the concentration
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of transmitter in the synaptic cleft (to be connected to pointer C here).
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-----------------------------------------------------------------------------
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Based on models
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Destexhe, A., Mainen, Z.F. and Sejnowski, T.J. Kinetic models of
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synaptic transmission. In: Methods in Neuronal Modeling (2nd edition;
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edited by Koch, C. and Segev, I.), MIT press, Cambridge, 1998, pp. 1-25.
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(electronic copy available at http://cns.iaf.cnrs-gif.fr)
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Written by Alain Destexhe, Laval University, 1995
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-----------------------------------------------------------------------------
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Modified Paul Manis, UNC Chapel Hill, 2009
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Changed name, pointer name, kinetics are range variables, and kinetic values
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are estimated from VCN glycine receptors.
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This model does not have a desensitization state.
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-----------------------------------------------------------------------------
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ENDCOMMENT
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INDEPENDENT {t FROM 0 TO 1 WITH 1 (ms)}
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NEURON {
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POINT_PROCESS GLYa5
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POINTER XMTR
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RANGE C0, C1, C2, O1, O2, Open
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RANGE g, gmax, f1, f2
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RANGE Erev
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RANGE kf1, kf2, kb1, kb2, a1, b1, a2, b2
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NONSPECIFIC_CURRENT i
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}
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UNITS {
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(nA) = (nanoamp)
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(mV) = (millivolt)
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(pS) = (picosiemens)
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(umho) = (micromho)
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(mM) = (milli/liter)
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(uM) = (micro/liter)
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}
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PARAMETER {
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Erev = -70 (mV) : reversal potential
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gmax = 500 (pS) : maximal conductance
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: Rates
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: from fits to averaged ipsc data, stellate cells 1/1/10
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: kf1 = 0.002930 (/uM /ms) : binding
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: kf2 = 0.005936 (/uM /ms) : binding
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: kb1 = 2.793 (/ms) : unbinding
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: kb2 = 1.445 (/ms) : unbinding
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: a1 = 1e-6 (/ms) : opening
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: b1 = 129.0 (/ms) : closing
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: a2 = 5.10 (/ms) : opening
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: b2 = 2.79 (/ms) : closing
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: from fits to averaged ipsc data, bushy cells 1/1/10
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kf1 = 0.0278 (/uM /ms) : binding
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kf2 = 1e-6 (/uM /ms) : binding
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kb1 = 0.000054 (/ms) : unbinding
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kb2 = 0.000855 (/ms) : unbinding
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a1 = 1e-6 (/ms) : opening
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b1 = 129.0 (/ms) : closing
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a2 = 5.10 (/ms) : opening
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b2 = 2.79 (/ms) : closing
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}
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ASSIGNED {
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v (mV) : postsynaptic voltage
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i (nA) : current = g*(v - Erev)
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g (pS) : conductance
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XMTR (mM) : pointer to glycine concentration
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f1 (/ms) : binding
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f2 (/ms) : binding
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Open (1)
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}
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STATE {
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: Channel states (all fractions)
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C0 : unbound
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C1 : single bound
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C2 : double bound
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O1 : open
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O2 : open
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}
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INITIAL {
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C0 = 1
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C1 = 0
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C2 = 0
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O1 = 0
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O2 = 0
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XMTR = 0.0
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}
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BREAKPOINT {
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SOLVE kstates METHOD sparse
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Open = (O1 + O2)
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g = gmax * Open
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i = (1e-6) * g * (v - Erev)
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}
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KINETIC kstates {
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f1 = kf1 * (1e3) * XMTR
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f2 = kf2 * (1e3) * XMTR
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~ C0 <-> C1 (f1,kb1)
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~ C1 <-> C2 (f2,kb2)
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~ C1 <-> O1 (a1,b1)
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~ C2 <-> O2 (a2,b2)
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CONSERVE C0+C1+C2+O1+O2 = 1
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}
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