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1 function method=MAPparamsNormal ...
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2 (BFlist, sampleRate, showParams)
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3 % MAPparams<> establishes a complete set of MAP parameters
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4 % Parameter file names must be of the form <MAPparams> <name>
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5 %
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6 % input arguments
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7 % BFlist (optional) specifies the desired list of channel BFs
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8 % otherwise defaults set below
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9 % sampleRate (optional), default is 50000.
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10 % showParams (optional) =1 prints out the complete set of parameters
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11 % output argument
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12 % method passes a miscelleny of values
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13
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14 global inputStimulusParams OMEParams DRNLParams
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15 global IHC_VResp_VivoParams IHCpreSynapseParams AN_IHCsynapseParams
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16 global MacGregorParams MacGregorMultiParams filteredSACFParams
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17 global experiment % used by calls from multiThreshold only
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18 global IHC_cilia_RPParams
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19
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20 currentFile=mfilename; % i.e. the name of this mfile
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21 method.parameterSource=currentFile(10:end); % for the record
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22
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23 efferentDelay=0.010;
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24 method.segmentDuration=efferentDelay;
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25
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26 if nargin<3, showParams=0; end
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27 if nargin<2, sampleRate=50000; end
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28 if nargin<1 || BFlist(1)<0 % if BFlist= -1, set BFlist to default
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29 lowestBF=250; highestBF= 8000; numChannels=21;
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30 % 21 chs (250-8k)includes BFs at 250 500 1000 2000 4000 8000
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31 BFlist=round(logspace(log10(lowestBF),log10(highestBF),numChannels));
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32 end
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33 % BFlist=1000;
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34
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35 % preserve for backward campatibility
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36 method.nonlinCF=BFlist;
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37 method.dt=1/sampleRate;
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38
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39 %%%%%%%%%%%%%%%%%%%%%%%%%%%%
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40 % set model parameters
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41 %%%%%%%%%%%%%%%%%%%%%%%%%%%%
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42
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43 %% #1 inputStimulus
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44 inputStimulusParams=[];
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45 inputStimulusParams.sampleRate= sampleRate;
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46
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47 %% #2 outerMiddleEar
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48 OMEParams=[]; % clear the structure first
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49 % outer ear resonances band pass filter [gain lp order hp]
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50 OMEParams.externalResonanceFilters= [ 10 1 1000 4000];
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51
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52 % highpass stapes filter
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53 % Huber gives 2e-9 m at 80 dB and 1 kHz (2e-13 at 0 dB SPL)
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54 OMEParams.OMEstapesLPcutoff= 1000;
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55 OMEParams.stapesScalar= 45e-9;
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56
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57 % Acoustic reflex: maximum attenuation should be around 25 dB Price (1966)
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58 % i.e. a minimum ratio of 0.056.
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59 % 'spikes' model: AR based on brainstem spiking activity (LSR)
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60 OMEParams.rateToAttenuationFactor=0.006; % * N(all ICspikes)
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61 % OMEParams.rateToAttenuationFactor=0; % * N(all ICspikes)
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62
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63 % 'probability model': Ar based on AN firing probabilities (LSR)
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64 OMEParams.rateToAttenuationFactorProb=0.003;% * N(all ANrates)
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65 % OMEParams.rateToAttenuationFactorProb=0;% * N(all ANrates)
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66
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67 % asymptote should be around 100-200 ms
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68 OMEParams.ARtau=.05; % AR smoothing function
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69 % delay must be longer than the segment length
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70 OMEParams.ARdelay=efferentDelay; %Moss gives 8.5 ms latency
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71 OMEParams.ARrateThreshold=0;
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72
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73 %% #3 DRNL
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74 DRNLParams=[]; % clear the structure first
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75 DRNLParams.BFlist=BFlist;
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76
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77 % DRNL nonlinear path
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78 DRNLParams.a=5e4; % DRNL.a=0 means no OHCs (no nonlinear path)
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79
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80 DRNLParams.b=8e-6; % *compression threshold raised compression
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81 % DRNLParams.b=1; % b=1 means no compression
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82
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83 DRNLParams.c=0.2; % compression exponent
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84 % nonlinear filters
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85 DRNLParams.nonlinCFs=BFlist;
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86 DRNLParams.nonlinOrder= 3; % order of nonlinear gammatone filters
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87 p=0.2895; q=170; % human (% p=0.14; q=366; % cat)
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88 DRNLParams.nlBWs= p * BFlist + q;
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89 DRNLParams.p=p; DRNLParams.q=q; % save p and q for printing only
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90
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91 % DRNL linear path:
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92 DRNLParams.g=100; % linear path gain factor
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93 % linCF is not necessarily the same as nonlinCF
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94 minLinCF=153.13; coeffLinCF=0.7341; % linCF>nonlinBF for BF < 1 kHz
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95 DRNLParams.linCFs=minLinCF+coeffLinCF*BFlist;
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96 DRNLParams.linOrder= 3; % order of linear gammatone filters
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97 minLinBW=100; coeffLinBW=0.6531;
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98 DRNLParams.linBWs=minLinBW + coeffLinBW*BFlist; % bandwidths of linear filters
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99
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100 % DRNL MOC efferents
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101 DRNLParams.MOCdelay = efferentDelay; % must be < segment length!
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102
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103 % 'spikes' model: MOC based on brainstem spiking activity (HSR)
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104 DRNLParams.rateToAttenuationFactor = .01; % strength of MOC
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105 % DRNLParams.rateToAttenuationFactor = 0; % strength of MOC
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106 % 'probability' model: MOC based on AN spiking activity (HSR)
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107 DRNLParams.rateToAttenuationFactorProb = .005; % strength of MOC
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108 % DRNLParams.rateToAttenuationFactorProb = .0; % strength of MOC
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109 DRNLParams.MOCrateThreshold =70; % spikes/s probability only
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110
|
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111 DRNLParams.MOCtau =.1; % smoothing for MOC
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112
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113
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114 %% #4 IHC_cilia_RPParams
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115
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116 IHC_cilia_RPParams.tc= 0.0003; % 0.0003 filter time simulates viscocity
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117 % IHC_cilia_RPParams.tc= 0.0005; % 0.0003 filter time simulates viscocity
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118 IHC_cilia_RPParams.C= 0.05; % 0.1 scalar (C_cilia )
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119 IHC_cilia_RPParams.u0= 5e-9;
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120 IHC_cilia_RPParams.s0= 30e-9;
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121 IHC_cilia_RPParams.u1= 1e-9;
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122 IHC_cilia_RPParams.s1= 1e-9;
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123
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124 IHC_cilia_RPParams.Gmax= 5e-9; % 2.5e-9 maximum conductance (Siemens)
|
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125 IHC_cilia_RPParams.Ga= 1e-9; % 4.3e-9 fixed apical membrane conductance
|
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126
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127 % #5 IHC_RP
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128 IHC_cilia_RPParams.Cab= 4e-012; % IHC capacitance (F)
|
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129 IHC_cilia_RPParams.Cab= 1e-012; % IHC capacitance (F)
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130 IHC_cilia_RPParams.Et= 0.100; % endocochlear potential (V)
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131
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132 IHC_cilia_RPParams.Gk= 2e-008; % 1e-8 potassium conductance (S)
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133 IHC_cilia_RPParams.Ek= -0.08; % -0.084 K equilibrium potential
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134 IHC_cilia_RPParams.Rpc= 0.04; % combined resistances
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135
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136
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137 %% #5 IHCpreSynapse
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138 IHCpreSynapseParams=[];
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139 IHCpreSynapseParams.GmaxCa= 14e-9;% maximum calcium conductance
|
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140 IHCpreSynapseParams.GmaxCa= 12e-9;% maximum calcium conductance
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141 IHCpreSynapseParams.ECa= 0.066; % calcium equilibrium potential
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142 IHCpreSynapseParams.beta= 400; % determine Ca channel opening
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143 IHCpreSynapseParams.gamma= 100; % determine Ca channel opening
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144 IHCpreSynapseParams.tauM= 0.00005; % membrane time constant ?0.1ms
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145 IHCpreSynapseParams.power= 3;
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146 % reminder: changing z has a strong effect on HF thresholds (like Et)
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147 IHCpreSynapseParams.z= 2e42; % scalar Ca -> vesicle release rate
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148
|
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149 LSRtauCa=35e-6; HSRtauCa=85e-6; % seconds
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150 % LSRtauCa=35e-6; HSRtauCa=70e-6; % seconds
|
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151 IHCpreSynapseParams.tauCa= [LSRtauCa HSRtauCa]; %LSR and HSR fiber
|
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152
|
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153 %% #6 AN_IHCsynapse
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154 % c=kym/(y(l+r)+kl) (spontaneous rate)
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155 % c=(approx) ym/l (saturated rate)
|
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156 AN_IHCsynapseParams=[]; % clear the structure first
|
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157 AN_IHCsynapseParams.M= 12; % maximum vesicles at synapse
|
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158 AN_IHCsynapseParams.y= 4; % depleted vesicle replacement rate
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159 AN_IHCsynapseParams.y= 6; % depleted vesicle replacement rate
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160
|
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161 AN_IHCsynapseParams.x= 30; % replenishment from re-uptake store
|
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162 AN_IHCsynapseParams.x= 60; % replenishment from re-uptake store
|
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163
|
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164 % reduce l to increase saturated rate
|
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165 AN_IHCsynapseParams.l= 100; % *loss rate of vesicles from the cleft
|
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166 AN_IHCsynapseParams.l= 250; % *loss rate of vesicles from the cleft
|
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167
|
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168 AN_IHCsynapseParams.r= 500; % *reuptake rate from cleft into cell
|
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169 % AN_IHCsynapseParams.r= 300; % *reuptake rate from cleft into cell
|
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170
|
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171 AN_IHCsynapseParams.refractory_period= 0.00075;
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172 % number of AN fibers at each BF (used only for spike generation)
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173 AN_IHCsynapseParams.numFibers= 100;
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174 AN_IHCsynapseParams.TWdelay=0.004; % ?delay before stimulus first spike
|
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175
|
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176 AN_IHCsynapseParams.ANspeedUpFactor=5; % longer epochs for computing spikes.
|
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|
177
|
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178 %% #7 MacGregorMulti (first order brainstem neurons)
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179 MacGregorMultiParams=[];
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180 MacGregorMultiType='chopper'; % MacGregorMultiType='primary-like'; %choose
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181 switch MacGregorMultiType
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182 case 'primary-like'
|
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183 MacGregorMultiParams.nNeuronsPerBF= 10; % N neurons per BF
|
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184 MacGregorMultiParams.type = 'primary-like cell';
|
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185 MacGregorMultiParams.fibersPerNeuron=4; % N input fibers
|
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186 MacGregorMultiParams.dendriteLPfreq=200; % dendritic filter
|
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187 MacGregorMultiParams.currentPerSpike=0.11e-6; % (A) per spike
|
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188 MacGregorMultiParams.Cap=4.55e-9; % cell capacitance (Siemens)
|
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189 MacGregorMultiParams.tauM=5e-4; % membrane time constant (s)
|
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190 MacGregorMultiParams.Ek=-0.01; % K+ eq. potential (V)
|
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191 MacGregorMultiParams.dGkSpike=3.64e-5; % K+ cond.shift on spike,S
|
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192 MacGregorMultiParams.tauGk= 0.0012; % K+ conductance tau (s)
|
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193 MacGregorMultiParams.Th0= 0.01; % equilibrium threshold (V)
|
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194 MacGregorMultiParams.c= 0.01; % threshold shift on spike, (V)
|
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195 MacGregorMultiParams.tauTh= 0.015; % variable threshold tau
|
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196 MacGregorMultiParams.Er=-0.06; % resting potential (V)
|
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197 MacGregorMultiParams.Eb=0.06; % spike height (V)
|
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|
198
|
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199 case 'chopper'
|
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200 MacGregorMultiParams.nNeuronsPerBF= 10; % N neurons per BF
|
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201 MacGregorMultiParams.type = 'chopper cell';
|
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|
202 MacGregorMultiParams.fibersPerNeuron=10; % N input fibers
|
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|
203 % MacGregorMultiParams.fibersPerNeuron=6; % N input fibers
|
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|
204
|
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205 MacGregorMultiParams.dendriteLPfreq=50; % dendritic filter
|
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|
206 MacGregorMultiParams.currentPerSpike=35e-9; % *per spike
|
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|
207 MacGregorMultiParams.currentPerSpike=30e-9; % *per spike
|
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|
208
|
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209 MacGregorMultiParams.Cap=1.67e-8; % ??cell capacitance (Siemens)
|
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210 MacGregorMultiParams.tauM=0.002; % membrane time constant (s)
|
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|
211 MacGregorMultiParams.Ek=-0.01; % K+ eq. potential (V)
|
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|
212 MacGregorMultiParams.dGkSpike=1.33e-4; % K+ cond.shift on spike,S
|
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|
213 MacGregorMultiParams.tauGk= 0.0005;% K+ conductance tau (s)
|
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214 MacGregorMultiParams.Th0= 0.01; % equilibrium threshold (V)
|
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215 MacGregorMultiParams.c= 0; % threshold shift on spike, (V)
|
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216 MacGregorMultiParams.tauTh= 0.02; % variable threshold tau
|
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217 MacGregorMultiParams.Er=-0.06; % resting potential (V)
|
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218 MacGregorMultiParams.Eb=0.06; % spike height (V)
|
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219 MacGregorMultiParams.PSTHbinWidth= 1e-4;
|
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220 end
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221
|
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222 %% #8 MacGregor (second-order neuron). Only one per channel
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223 MacGregorParams=[]; % clear the structure first
|
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224 MacGregorParams.type = 'chopper cell';
|
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225 MacGregorParams.fibersPerNeuron=10; % N input fibers
|
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226 MacGregorParams.dendriteLPfreq=100; % dendritic filter
|
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|
227 MacGregorParams.currentPerSpike=120e-9;% *(A) per spike
|
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|
228 MacGregorParams.currentPerSpike=30e-9;% *(A) per spike
|
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|
229
|
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230 MacGregorParams.Cap=16.7e-9; % cell capacitance (Siemens)
|
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231 MacGregorParams.tauM=0.002; % membrane time constant (s)
|
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232 MacGregorParams.Ek=-0.01; % K+ eq. potential (V)
|
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233 MacGregorParams.dGkSpike=1.33e-4; % K+ cond.shift on spike,S
|
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|
234 MacGregorParams.tauGk= 0.0005; % K+ conductance tau (s)
|
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|
235 MacGregorParams.Th0= 0.01; % equilibrium threshold (V)
|
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236 MacGregorParams.c= 0; % threshold shift on spike, (V)
|
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237 MacGregorParams.tauTh= 0.02; % variable threshold tau
|
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238 MacGregorParams.Er=-0.06; % resting potential (V)
|
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239 MacGregorParams.Eb=0.06; % spike height (V)
|
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240 MacGregorParams.debugging=0; % (special)
|
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|
241 % wideband accepts input from all channels (of same fiber type)
|
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|
242 % use wideband to create inhibitory units
|
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|
243 MacGregorParams.wideband=0; % special for wideband units
|
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|
244 % MacGregorParams.saveAllData=0;
|
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|
245
|
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246 %% #9 filteredSACF
|
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247 minPitch= 300; maxPitch= 3000; numPitches=60; % specify lags
|
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248 pitches=100*log10(logspace(minPitch/100, maxPitch/100, numPitches));
|
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|
249 filteredSACFParams.lags=1./pitches; % autocorrelation lags vector
|
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|
250 filteredSACFParams.acfTau= .003; % time constant of running ACF
|
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|
251 filteredSACFParams.lambda= 0.12; % slower filter to smooth ACF
|
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|
252 filteredSACFParams.plotFilteredSACF=1; % 0 plots unfiltered ACFs
|
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|
253 filteredSACFParams.plotACFs=0; % special plot (see code)
|
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|
254 % filteredSACFParams.usePressnitzer=0; % attenuates ACF at long lags
|
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|
255 filteredSACFParams.lagsProcedure= 'useAllLags';
|
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|
256 % filteredSACFParams.lagsProcedure= 'useBernsteinLagWeights';
|
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|
257 % filteredSACFParams.lagsProcedure= 'omitShortLags';
|
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258 filteredSACFParams.criterionForOmittingLags=3;
|
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|
259
|
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|
260 % checks
|
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|
261 if AN_IHCsynapseParams.numFibers<MacGregorMultiParams.fibersPerNeuron
|
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|
262 error('MacGregorMulti: too few input fibers for input to MacG unit')
|
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|
263 end
|
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|
264
|
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|
265
|
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266 %% write all parameters to the command window
|
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|
267 % showParams is currently set at the top of htis function
|
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|
268 if showParams
|
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269 fprintf('\n %%%%%%%%\n')
|
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|
270 fprintf('\n%s\n', method.parameterSource)
|
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|
271 fprintf('\n')
|
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|
272 nm=UTIL_paramsList(whos);
|
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|
273 for i=1:length(nm)
|
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|
274 % eval(['UTIL_showStruct(' nm{i} ', ''' nm{i} ''')'])
|
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|
275 if ~strcmp(nm(i), 'method')
|
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|
276 eval(['UTIL_showStructureSummary(' nm{i} ', ''' nm{i} ''', 10)'])
|
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|
277 end
|
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|
278 end
|
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|
279 end
|
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|
280
|
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|
281
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rmeddis@0
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282
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rmeddis@0
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283 % ********************************************************************** comparison data
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284 % store individual data here for display on the multiThreshold GUI (if used)
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285 % the final value in each vector is an identifier (BF or duration))
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286 if isstruct(experiment)
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287 switch experiment.paradigm
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288 case {'IFMC','IFMC_8ms'}
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289 % based on MPa
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290 comparisonData=[
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291 66 51 49 48 46 45 54 250;
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rmeddis@0
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292 60 54 46 42 39 49 65 500;
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293 64 51 38 32 33 59 75 1000;
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rmeddis@0
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294 59 51 36 30 41 81 93 2000;
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rmeddis@0
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295 71 63 53 44 36 76 95 4000;
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rmeddis@0
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296 70 64 43 35 35 66 88 6000;
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297 110 110 110 110 110 110 110 8000;
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298 ];
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299 if length(BFlist)==1 && ~isempty(comparisonData)
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300 availableFrequencies=comparisonData(:,end)';
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301 findRow= find(BFlist==availableFrequencies);
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302 if ~isempty (findRow)
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303 experiment.comparisonData=comparisonData(findRow,:);
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304 end
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305 end
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|
306
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|
307 case {'TMC','TMC_8ms'}
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|
308 % based on MPa
|
rmeddis@0
|
309 comparisonData=[
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|
310 48 58 63 68 75 80 85 92 99 250;
|
rmeddis@0
|
311 33 39 40 49 52 61 64 77 79 500;
|
rmeddis@0
|
312 39 42 50 81 83 92 96 97 110 1000;
|
rmeddis@0
|
313 24 26 32 37 46 51 59 71 78 2000;
|
rmeddis@0
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314 65 68 77 85 91 93 110 110 110 4000;
|
rmeddis@0
|
315 20 19 26 44 80 95 96 110 110 6000;
|
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|
316 ];
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317 if length(BFlist)==1 && ~isempty(comparisonData)
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|
318 availableFrequencies=comparisonData(:,end)';
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319 findRow= find(BFlist==availableFrequencies);
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|
320 if ~isempty (findRow)
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321 experiment.comparisonData=comparisonData(findRow,:);
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322 end
|
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|
323 end
|
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|
324
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325 case { 'absThreshold', 'absThreshold_8'}
|
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|
326 % MPa thresholds
|
rmeddis@0
|
327 experiment.comparisonData=[
|
rmeddis@0
|
328 32 26 16 18 22 22 0.008;
|
rmeddis@0
|
329 16 13 6 9 15 11 0.500
|
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|
330 ];
|
rmeddis@0
|
331
|
rmeddis@0
|
332
|
rmeddis@0
|
333 otherwise
|
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|
334 experiment.comparisonData=[];
|
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|
335 end
|
rmeddis@0
|
336 end
|
rmeddis@0
|
337
|
rmeddis@0
|
338
|