Dopamine-modulated medium spiny neuron, reduced model (Humphries et al. 2009)

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Accession:128818
We extended Izhikevich's reduced model of the striatal medium spiny neuron (MSN) to account for dopaminergic modulation of its intrinsic ion channels and synaptic inputs. We tuned our D1 and D2 receptor MSN models using data from a recent (Moyer et al, 2007) large-scale compartmental model. Our new models capture the input-output relationships for both current injection and spiking input with remarkable accuracy, despite the order of magnitude decrease in system size. They also capture the paired pulse facilitation shown by MSNs. Our dopamine models predict that synaptic effects dominate intrinsic effects for all levels of D1 and D2 receptor activation. Our analytical work on these models predicts that the MSN is never bistable. Nonetheless, these MSN models can produce a spontaneously bimodal membrane potential similar to that recently observed in vitro following application of NMDA agonists. We demonstrate that this bimodality is created by modelling the agonist effects as slow, irregular and massive jumps in NMDA conductance and, rather than a form of bistability, is due to the voltage-dependent blockade of NMDA receptors
Reference:
1 . Humphries MD, Lepora N, Wood R, Gurney K (2009) Capturing dopaminergic modulation and bimodal membrane behaviour of striatal medium spiny neurons in accurate, reduced models. Front Comput Neurosci 3:26 [PubMed]
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:
Cell Type(s): Neostriatum medium spiny direct pathway GABA cell;
Channel(s):
Gap Junctions:
Receptor(s): D1; D2; GabaA; AMPA; NMDA;
Gene(s):
Transmitter(s): Dopamine;
Simulation Environment: MATLAB;
Model Concept(s): Action Potential Initiation; Parameter Fitting; Simplified Models; Parkinson's; Bifurcation;
Implementer(s): Humphries, Mark D [m.d.humphries at shef.ac.uk];
Search NeuronDB for information about:  Neostriatum medium spiny direct pathway GABA cell; D1; D2; GabaA; AMPA; NMDA; Dopamine;
%%%% script to show effects of D2 intrinsic model

clear all
cl_fig

% found values
% basic tuned model from stage 1....
load fit_model_results_NEWtuning
k = izipars(1); a = izipars(2); b = izipars(3); c = izipars(4); vr = izipars(5); vpeak = izipars(6);

% found MS parameters: X = [C,vt,d]
C = X(1); vt =X(2); d = X(3);

% extra DA model parameters in saved file
alpha = XD2(1);   

% parameters for this test
I = 200:5:400;
nInj = numel(I);

D2 = 0:0.2:1;

% init simulation 
T = 5000; % duration of simulation (milliseconds)
dt = 0.1; % time step
t = 0:dt:T;
n = length(t); % number of time points
f_start = 1000/dt;
f_end = T/dt;
f_time = (f_end - f_start) * 1e-3 * dt;

%% f-I curves
fID2_DA = zeros(numel(D2),nInj);
fI1stD2_DA = zeros(numel(D2),nInj);
for j = 1:numel(D2)
    for loop = 1:nInj
        loop
        vD2 = vr*ones(1,n); uD2=0*vD2;
        kD2 = k * (1-alpha*D2(j));    
        
        for i = 1:n-1
            %--- D2 type                        
            vD2(i+1) = vD2(i) + dt*(kD2*(vD2(i)-vr)*(vD2(i)-vt)-uD2(i) + I(loop))/C;

            uD2(i+1) = uD2(i) + dt*a*(b*(vD2(i)-vr)-uD2(i));
            % spikes?   
            if vD2(i+1)>=vpeak
                vD2(i)=vpeak; vD2(i+1)=c; 
                uD2(i+1)=uD2(i+1)+d;
            end
        end
       % firing rate at this frequency
        fID2_DA(j,loop) = sum(vD2(f_start:f_end) == vpeak) ./ f_time;
        temp = find(vD2 == vpeak); isis = diff(temp)*dt;
        if isis fI1stD2_DA(j,loop) = 1000./isis(1); else fI1stD2_DA(j,loop) = 0; end
        
    end
end

figure(2); clf
plot(I,fID2_DA); hold on
plot(I,fI1stD2_DA,':')


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