Mercurial > hg > map
view testPrograms/testRP.m @ 38:c2204b18f4a2 tip
End nov big change
author | Ray Meddis <rmeddis@essex.ac.uk> |
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date | Mon, 28 Nov 2011 13:34:28 +0000 |
parents | 3ea506487b3b |
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function testRP(BFs,MAPparamsName,paramChanges) % testIHC evaluates IHC I/O function % multiple BFs can be used but only one is easier to interpret. % e.g. testRP(1000,'Normal',{}); global experiment method inputStimulusParams global stimulusParameters IHC_VResp_VivoParams IHC_cilia_RPParams savePath=path; addpath (['..' filesep 'utilities'],['..' filesep 'MAP']) dbstop if error figure(4), clf, set (gcf, 'name', ['IHC']) set(gcf,'position',[613 354 360 322]) drawColors='rgbkmcy'; drawnow if nargin<3 paramChanges=[]; end if nargin<2 MAPparamsName='Normal'; end if nargin<3 BFs=800; end levels=-20:10:100; nLevels=length(levels); toneDuration=.05; silenceDuration=.01; sampleRate=50000; dt=1/sampleRate; allIHC_RP_peak=[]; allIHC_RP_dc=[]; for BFno=1:length(BFs) BF=BFs(BFno); targetFrequency=BF; % OR %Patuzzi and Sellick test (see ELP & AEM, 2006) % targetFrequency=100; IHC_RP_peak=zeros(nLevels,1); IHC_RP_min=zeros(nLevels,1); IHC_RP_dc=zeros(nLevels,1); time=dt:dt:toneDuration; rampDuration=0.004; rampTime=dt:dt:rampDuration; ramp=[0.5*(1+cos(2*pi*rampTime/(2*rampDuration)+pi)) ... ones(1,length(time)-length(rampTime))]; ramp=ramp.*fliplr(ramp); silence=zeros(1,round(silenceDuration/dt)); toneStartptr=length(silence)+1; toneMidptr=toneStartptr+round(toneDuration/(2*dt)) -1; toneEndptr=toneStartptr+round(toneDuration/dt) -1; levelNo=0; for leveldB=levels levelNo=levelNo+1; % replicate at all levels amp=28e-6*10^(leveldB/20); %% create signal (leveldB/ frequency) inputSignal=amp*sin(2*pi*targetFrequency'*time); inputSignal= ramp.*inputSignal; inputSignal=[silence inputSignal silence]; inputStimulusParams.sampleRate=1/dt; % global IHC_ciliaParams %% disable efferent for fast processing method.DRNLSave=1; method.IHC_cilia_RPSave=1; method.IHCpreSynapseSave=1; method.IHC_cilia_RPSave=1; method.segmentDuration=-1; moduleSequence=1:4; %% run the model global DRNLoutput IHC_cilia_output IHCrestingCiliaCond IHCrestingV... IHCoutput AN_spikesOrProbability='probability'; MAP1_14(inputSignal, sampleRate, BF, ... MAPparamsName, AN_spikesOrProbability, paramChanges); % DRNL DRNLoutput=DRNLoutput; DRNL_peak(levelNo,1)=max(DRNLoutput(toneMidptr:toneEndptr)); DRNL_min(levelNo,1)=min(DRNLoutput(toneMidptr:toneEndptr)); DRNL_dc(levelNo,1)=mean(DRNLoutput(toneMidptr:toneEndptr)); % cilia IHC_ciliaData=IHC_cilia_output; IHC_ciliaData=IHC_ciliaData; IHC_cilia_peak(levelNo,1)=... max(IHC_ciliaData(toneMidptr:toneEndptr)); IHC_cilia_min(levelNo,1)=... min(IHC_ciliaData(toneMidptr:toneEndptr)); IHC_cilia_dc(levelNo,1)=... mean(IHC_ciliaData(toneMidptr:toneEndptr)); % RP IHC_RPData=IHCoutput; IHC_RPData=IHC_RPData; IHC_RP_peak(levelNo,1)=... max(IHC_RPData(toneMidptr:toneEndptr)); IHC_RP_min(levelNo,1)=... min(IHC_RPData(toneMidptr:toneEndptr)); IHC_RP_dc(levelNo,1)=... mean(IHC_RPData(toneMidptr:toneEndptr)); end % level disp(['parameter file was: ' MAPparamsName]) fprintf('\n') %% plot DRNL subplot(2,2,1) % referenceDisp= 9e-9*1000/targetFrequency; % plot(levels,20*log10(DRNL_peak/referenceDisp), drawColors(BFno), ... % 'linewidth',2), hold on referenceDisp=10e-9; plot(levels,20*log10(DRNL_peak/referenceDisp), drawColors(BFno), ... 'linewidth',2), hold on title([' DRNL peak: ' num2str(BFs) ' Hz']) ylabel ('log10DRNL(m)'), xlabel('dB SPL') xlim([min(levels) max(levels)]), ylim([-10 50]) grid on %% plot cilia displacement figure(4) subplot(2,2,2) restingIHC_cilia=IHCrestingCiliaCond; plot(levels, IHC_cilia_peak,'k', 'linewidth',2), hold on % plot(levels, IHC_cilia_min,'r', 'linewidth',2) % hold on, % plot([min(levels) max(levels)], ... % [restingIHC_cilia restingIHC_cilia], 'g') title(' IHC apical cond.') ylabel ('IHCcilia(conductance)'), xlabel('dB SPL') xlim([min(levels) max(levels)]) grid on %% plot receptor potentials figure(4) subplot(2,2,3) % RP I/O function min and max restingRP=IHC_RP_peak(1); toPlot= [fliplr(IHC_RP_min(:,1)') IHC_RP_peak(:,1)']; microPa= 28e-6*10.^(levels/20); microPa=[-fliplr(microPa) microPa]; plot(microPa,toPlot, drawColors(BFno), 'linewidth',2) % ylim([0 300]) %% Dallos and Harris data dallosx=[-0.9 -0.1 -0.001 0.001 0.01 0.9]; dallosy=[-8 -7.8 -6.5 11 16.5 22]/1000 + restingRP; hold on, plot(dallosx,dallosy, 'o') plot([-1 1], [restingRP restingRP], 'r') title(' Dallos(86) data at 800 Hz') ylabel ('receptor potential(V)'), xlabel('Pa') ylim([-0.08 -0.02]), xlim([-1 1]) grid on %% RP I/O function min and max figure(4) subplot(2,2,4) restingRP=IHC_RP_peak(1); peakRP=max(IHC_RP_peak); plot(levels, IHC_RP_peak,drawColors(BFno), 'linewidth',2) hold on plot(levels, IHC_RP_dc, [drawColors(BFno) ':'], 'linewidth',2) hold on, plot([min(levels) max(levels)], [restingRP restingRP], 'r') xlim([min(levels) max(levels)]) % animal data sndLevel=[5 15 25 35 45 55 65 75]; RPanimal=restingRP+[0.5 2 4.6 5.8 6.4 7.2 8 10.2]/1000; % could be misleading when restingRP changes RPanimal=-0.060+[0.5 2 4.6 5.8 6.4 7.2 8 10.2]/1000; hold on, plot(sndLevel,RPanimal,'o') grid on title(['Et= ' num2str(IHC_cilia_RPParams.Et) ': RP data 7 kHz Patuzzi']) ylabel ('RP(V) peak and DC'), xlabel('dB SPL') ylim([-0.08 -0.04]) allIHC_RP_peak=[allIHC_RP_peak IHC_RP_peak]; allIHC_RP_dc=[allIHC_RP_dc IHC_RP_dc]; fprintf('level\t peak\t DC\n') UTIL_printTabTable([levels' IHC_RP_peak IHC_RP_dc]) % disp(['restingIHC_cilia= ' num2str(restingIHC_cilia)]) fprintf('peakRP= \t%6.3f', peakRP) fprintf('\nrestingRP= \t%6.3f', restingRP) fprintf('\ndifference= \t%6.3f\n', (peakRP-restingRP)) drawnow end % UTIL_showStruct(IHC_VResp_VivoParams, 'IHC_VResp_VivoParams') UTIL_showStruct(IHC_cilia_RPParams, 'IHC_cilia_RPParams') fprintf('level\t peak\n') UTIL_printTabTable([levels' allIHC_RP_peak]) fprintf('level\t DC\n') UTIL_printTabTable([levels' allIHC_RP_dc]) path(savePath); disp(paramChanges)