Contrast Gain Reduction in Fly Motion Adaptation

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Contrast Gain Reduction in Fly Motion Adaptation Robert A. Harris, David C. O'Carroll, Simon B. Laughlin  Neuron  Volume 28, Issue 2, Pages 595-606 (November 2000) DOI: 10.1016/S0896-6273(00)00136-7

Figure 1 Motion Adaptation in Fly HS Cells (A) Example response of an HS cell to the motion adaptation protocol. A sinusoidal grating (30% contrast, 5 Hz temporal frequency, 0.1 cycles/° spatial frequency) is presented during the first test period, followed by a 4 s presentation of a strongly adapting stimulus (sinusoidal grating, 95% contrast, 20 Hz, 0.02 cycles/°). The test stimulus is then immediately represented. The response to the test grating is much reduced after adaptation. (B) Responses of HS cells to test gratings of different contrasts before and after adaptation (protocol as in [A], means and standard errors, n = 15 trials, 12 cells). Test and adapting stimuli presented in preferred direction. Responses calculated as the mean membrane potential between 100 and 300 ms following onset of the test stimuli as indicated by shaded bars in (A) (see Experimental Procedures). Responses for each cell were normalized to an unadapted resting potential of 0 and a maximum unadapted response of 1. Neuron 2000 28, 595-606DOI: (10.1016/S0896-6273(00)00136-7)

Figure 2 Contrast-Response Functions of HS Cells before and after Adaptation to Preferred and Anti-Preferred Direction Motion Example traces shown on left. Means and standard errors for three cells. (A) Response to preferred direction test stimuli before adaptation (closed circles) and after adaptation with either preferred direction motion (open circles) or anti-preferred direction motion (open squares). (B) Response to anti-preferred direction test stimuli (same key). Each cell's responses were normalized to an unadapted resting potential of 0 and either a maximum unadapted response of 1 (for preferred direction test stimuli), or a minimum of −1 (for anti-preferred direction test stimuli). Neuron 2000 28, 595-606DOI: (10.1016/S0896-6273(00)00136-7)

Figure 6 Responses of HS Cells before and after Adaptation to Other Directions of Motion (A) Example response of an HS cell to preferred direction test gratings before and after adaptation with a grating (95%, 20 Hz, 0.1 cycles/°) moving at 79° to the cell's preferred direction. (B) Response magnitude of the same HS cell to a moderate contrast (30%) preferred direction grating before (closed circles) and after (open circles) adaptation to gratings at different orientations. Also shown is the response evoked during the adapting period (triangles). All adapting orientations cause a large reduction in test response magnitude. Analysis windows illustrated by shaded bars in (A). Neuron 2000 28, 595-606DOI: (10.1016/S0896-6273(00)00136-7)

Figure 3 Method Used to Quantify Changes in the Cell's Contrast Sensitivity following Adaptation The total change in the cell's contrast sensitivity (ΔCStotal) is given by the ratio of the contrasts required to elicit a criterion response before and after adaptation (Cadapted divided by Cunadapted). We also estimated the change in contrast sensitivity attributable to the “gain reduction” component of adaptation only (ΔCSgain) (i.e., the component causing the rightward shift of the curve on the log contrast axis). The after-potential is removed by normalizing the adapted curve such that the mean of the subthreshold responses is zero (giving the dashed curve). ΔCSgain is then determined by taking the ratio of Ccorrected to Cunadapted. Neuron 2000 28, 595-606DOI: (10.1016/S0896-6273(00)00136-7)

Figure 4 Contrast-Response Function of HS Cells following Adaptation to Motion or Flicker Mean and standard errors before adaptation (closed circles, n = 33 trials, 20 cells), after adaptation with preferred direction motion (sinusoidal grating, 20 Hz, 0.1 cycles/°, 95% contrast) (open circles, n = 15 trials, 12 cells), adaptation with wide-field flicker (sinusoidal modulation at 20 Hz, 95% contrast) (open squares, n = 8 trials, 7 cells), and adaptation with local flicker (counter-phasing sinusoidal grating, 95% contrast, 0.1 cycles/°, 20 Hz, see main text) (open triangles, n = 7 trials, 4 cells). Each cell's responses were normalized to an unadapted resting potential of 0 and a maximum unadapted response of 1. Neuron 2000 28, 595-606DOI: (10.1016/S0896-6273(00)00136-7)

Figure 5 Responses of HS Cells before and after Adaptation with Orthogonal Motion (A) Example responses of an HS cell to orthogonal motion adaptation (90° to the cell's preferred direction). An orthogonal adapting stimulus (95%, 20 Hz, 0.1 cycles/°) evokes little response from the cell. However, the response to a preferred direction test grating (top trace: 30% contrast, 5 Hz, 0.1 cycles/°; bottom trace: 50% contrast, 5 Hz, 0.1 cycles/°) is still greatly reduced following adaptation. (B) Contrast-response function of HS cells before (closed circles, n = 19 trials, 14 cells) and after adaptation to preferred direction motion (open circles, n = 12 trials, 10 cells) or orthogonal direction motion (90° or 270° to the cell's preferred direction, open squares, n = 7 trials, 6 cells). Neuron 2000 28, 595-606DOI: (10.1016/S0896-6273(00)00136-7)

Figure 7 Relationship between Activity Induced by Motion Stimulation (“Test-Potential”) and the Subsequent After-Potential (A) Example response to test stimulus; shaded bars illustrate analysis windows (50–250 ms following stimulus onset/offset, see Experimental Procedures). (B–E) Each point represents data from a single stimulus condition. The base test stimulus was a sinusoidal grating, 30% contrast, 0.1 cycles/°, 5 Hz moving in the preferred or anti-preferred direction (see Experimental Procedures). The cell was driven to different potentials by altering either (B) pattern contrast, (C) temporal frequency, (D) spatial frequency, or (E) grating direction. Table 2 shows the results of a correlation and regression analysis. Neuron 2000 28, 595-606DOI: (10.1016/S0896-6273(00)00136-7)