# XPP scripts for supplementary Figure S4C left of 
# Maex R, Grinevich VP, Grinevich V, Budygin E, Bencherif M, Gutkin B (2014)
# Understanding the role a7 nicotinic receptors play in dopamine efflux
# in nucleus accumbens. ACS Chemical Neuroscience 5, 1032-1040.
#
# Desensitization model of Figure 2B; varying the DC50 of a7 inactivation.

# Output is accumbal dopamine concentration in microM.


# Naming conventions 
#
# V_      = membrane voltage of (neuron or neuron population)
# R_      = release of (transmitter)
# C_      = concentration of (transmitter)
# I_      = membrane current of (channel or receptor)
# P_      = presynatic membrane current of (receptor)
# tau_    = time-constant of
# tmin_ = minimum value of time-constant of
# tmax_ = maximum value of time-constant of
# inf_    = steady-state value of
# act_    = level of activation of (receptor)
# des_    = level of desensitisation of (receptor)
# w_      = weight of
# EC50_   = halfmax concentration of steady-state response
# Ktau_   = halfmax concentration of time-constant
# stim_   = stimulation by

# glu  = glutamate or glu-ergic neuron (population)
# dop  = dopamine or dopamine-ergic neuron (population)
# gab  = gaba or gaba-ergic neuron (population)
# ach  = acetylcholine
# nic  = nicotine
# a7   = alpha7-type nicACh receptor
# a4b2 = alpha4-beta2-type nicACh receptor
# bas  = basal
#


# Units 
# time seconds
# concentration microMolar (nanoMolar in printed figures)


# Transfer functions (input-output) 
# sigmoid
f(x) = 1/(1 + exp(-x)) 
# halfwave rectification
hwr(x) = heav(x) * x    
# clipped at 0 and 1
clip(x) = (1 + (x-1) * (heav (1-x))) * heav(x) 
# Hill equation
# Hill(x,K,n) = 1 / (1 + (K/x)^n)
Hill(x,K,n) = x^n / (x^n + K^n) 
# competitive Hill ---THIS IS NEW and allows for competitive inhibition between up to three compounds --- 
compHill(x,y,z,wx,wy,wz,Kx,Ky,Kz,n) = \
  (wx * x^n/(x^n + Kx^n * (1 + (y/Ky)^n + (z/Kz)^n))) + \
  (wy * y^n/(y^n + Ky^n * (1 + (x/Kx)^n + (z/Kz)^n))) + \
  (wz * z^n/(z^n + Kz^n * (1 + (x/Kx)^n + (y/Ky)^n)))
# rectangular pulse
rect_pulse(t,from,to,amp) = amp * (heav (t-from) - heav (t-to))



# THE MODEL (some of this code is based on Graupner & Gutkin)

# We now have two neuron populations sharing inputs from
# glu neurons (mostly a7-driven) and through a4b2 receptors.
# The parameter coefficients r and s specify the balance 
# between these inputs.

   par s=0.8,r=0.8


# the dynamics of the dopaminergic neuron population V_dop

   V_dop' = (-V_dop - I_gab + hwr (I_basDop + s*I_glu + r*I_b2)) / tau_Vdop

   par tau_Vdop=0.02,I_basDop=0.1
   aux aux_hwr=hwr (I_basDop + s*I_glu + r*I_b2)


# the dynamics of the gaba-ergic neuron population V_gab

   V_gab' = (-V_gab + hwr ((1-s)*I_glu + (1-r)*I_b2)) / tau_Vgab

   par tau_Vgab=0.02


# the (stationary) glutamatergic input I_glu to dopamine (and GABA) neurons

   I_glu = w_glu * clip (V_glu + P_glu)

   par w_glu=1,V_glu=0.1


# the (varying) gaba-ergic input I_gab to dopamine neurons

   I_gab = w_gab * clip (V_gab + I_basGab)

   aux auxI_gab=I_gab
   par w_gab=1.5 
   par I_basGab=-0.05
   aux auxI_gab=I_gab

# the presynaptic facilitation of glu input to dopamine (and GABA) neurons

   P_glu = P_a7


# the dynamics of presynaptic a7 receptors (same single variable for 
# glu inputs to dopamine cells in VTA and medium spiny neurons in striatum)

   P_a7 = act_a7 * (1 - des_a7)
   aux auxP_a7=P_a7
   aux auxact_a7=act_a7
   aux auxsen_a7=1-des_a7


#   /* activation of alpha7 */

   act_a7' = (- act_a7 + inf_actA7) / tau_actA7

   inf_actA7 = compHill(C_ach,    C_nic,        C_agA7, \
                            1, w_actNicA7,   w_actAgA7, \
                   EC50_A7ach, EC50_A7nic,   EC50_A7ag, Hill_actA7)


   par EC50_A7=80
   par EC50_A7ach=68
   par EC50_A7nic=13
   par Hill_actA7=1.73
   par EC50_A7ag=0.03 
   par w_actNicA7=0.8 
   par w_actAgA7=0.3
   par tau_actA7=0.005


#   /* desensitisation of alpha7 */

   des_a7' = (- des_a7 + inf_desA7) / tau_desA7

   inf_desA7 = compHill(    0,      C_nic,      C_agA7, \
                            1,          1,           1, \
                            1, IC50_A7nic,   IC50_A7ag, Hill_desA7)

   par IC50_A7nic=1.3
   par Hill_desA7=2


# THIS IS THE PARAMETER VARIED IN THE FIGURE
   par IC50_A7ag=0.002
#   par IC50_A7ag=0.004
#   par IC50_A7ag=0.01
#   par IC50_A7ag=0.1

   tau_desA7 = tmin_desA7 + \ 
               tmax_desA7 * (1 - inf_desA7)
   aux aux_tdA7=tau_desA7

   par tmin_desA7=0.05
   par tmax_desA7=120


# the dynamics of somatic a4b2 receptors on the soma/dendrite of dopamine neurons

   I_b2 = act_b2 * (1 - des_b2)

   aux auxI_b2=I_b2
   aux auxact_b2=act_b2
   aux auxsen_b2=1-des_b2


#   /* activation of alpha4beta2 */

   act_b2' = (- act_b2 + inf_actB2) / tau_actB2

   inf_actB2 = compHill(C_ach,      C_nic,        C_agB2, \
                            1, w_actNicB2,   w_actAgB2, \
                   EC50_B2ach, EC50_B2nic,   EC50_B2ag, Hill_actB2)


   par EC50_actB2=30
   par EC50_B2ach=30
   par EC50_B2ag=30
   par EC50_B2nic=0.23
   par Hill_actB2=1.05
   par w_actNicB2=2
   par w_actAgB2=1
   par tau_actB2=0.005


#   /* desensitisation */

   des_b2' = (- des_b2 + inf_desB2) / tau_desB2

   inf_desB2 = Hill (C_nic + C_agB2, EC50_desB2, Hill_desB2)

   tau_desB2 = tmin_desB2 + \ 
               tmax_desB2 * Hill (Ktau_desB2, C_nic + C_agB2, Htau_desB2)

   aux aux_tdB2=tau_desB2

   par EC50_desB2=0.061
   par Hill_desB2=0.5
   par tmin_desB2=0.5
   par tmax_desB2=600
   par Ktau_desB2=0.11
   par Htau_desB2=3


# the dynamics of dopamine release AND RE-UPTAKE
# This is a bit complicated because for a fair comparison, all dopamine levels
# are normalized to the same fixed baseline (about 50 nanoMolar). Hence we assume
# that homeostatic mechanisms are at work that keep the baseline fixed under variable
# parameter conditions (mostly varying cholinergic tones).

   R_dop' = (C_basDop * (1 + (V_dop-ss_Vdop) / ss_Vdop) - R_dop) / tau_Rdop - R_dop * Vmax_Rdop / (R_dop + EC50_Rdop)

   par tau_Rdop=0.2,P_a7bas=0.01
   par C_basDop=0.1
# the following values are from Chen and Budygin 2007
   par Vmax_Rdop=1.3
   par EC50_Rdop=0.2


# the physiological (ach) and pharmacological (nic, specific a7 and a4b2 agonists) stimuli

#  /* acetylcoline */
   par C_ach=20
#   par C_ach=30

#   /* nicotine */
   stim_nic = bas_nic + rect_pulse (t, 66, 67, dose_Nic)
   par dose_Nic=5

# we now simulate an alpha function as a second-order ode
# the alpha-function is area normalized
# to calculate its peak, take amplitude and divide by 10*e

   C_nic_nic' = (-C_nic_nic + stim_nic)/tau1_nic
   C_nic' = (-C_nic + C_nic_nic)/tau2_nic

    par tau1_nic=10,tau2_nic=10,bas_nic=0 


#   /* alpha7 agonist */

   stim_a7 = rect_pulse (t, 36, 37, dose_Aga7)
   par dose_Aga7=0.3

   C_agA7A7' = (-C_agA7A7 + stim_a7) / tau1_agA7
   C_agA7' = (-C_agA7 + C_agA7A7) / tau2_agA7

   par tau1_agA7=10,tau2_agA7=10 


#   /* alpha4 beta2 agonist */

   stim_b2 = rect_pulse (t, 60, 61, 0)
   C_agB2' = (-C_agB2 + stim_b2) / tau_agB2

   par tau_agB2=10


# /* calculating the steady-states (in reverse order) */
    ss_Ib2 = compHill(   C_ach,          0,           0, \
                            1, w_actNicB2,   w_actAgB2, \
                   EC50_B2ach, EC50_B2nic,   EC50_B2ag, Hill_actB2)
    ss_Pa7 = compHill(   C_ach,          0,           0, \
                            1, w_actNicA7,   w_actAgA7, \
                   EC50_A7ach, EC50_A7nic,   EC50_A7ag, Hill_actA7)
    ss_Pglu = ss_Pa7
    ss_Iglu = w_glu * clip (V_glu + ss_Pglu)
    ss_Vgab = hwr ((1-s)*ss_Iglu + (1-r)*ss_Ib2)
    ss_Igab = w_gab * clip (ss_Vgab + I_basGab)
    ss_Vdop = - ss_Igab + hwr (I_basDop + s*ss_Iglu + r*ss_Ib2)
# aux auxss_Vdop=ss_Vdop


# the initial conditions
act_a7(0)=0
des_a7(0)=0
act_b2(0)=0
des_b2(0)=0
V_dop(0)=0
V_gab(0)=0
C_nic(0)=bas_nic
C_nic_nic(0)=bas_nic


# the numerical parameters
@ MAXSTOR=500000
@ BOUNDS=1e+8
@ DT=0.005
@ TOTAL=150
@ xlo=20
@ xhi=120
@ ylo=0
@ yhi=0.12
@ METHOD=rk
@ NJMP=20
@ YP=r_dop
done