Volume 39, Issue 2, Pages (July 2003)

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Volume 39, Issue 2, Pages 353-359 (July 2003) Coupling of Total Hemoglobin Concentration, Oxygenation, and Neural Activity in Rat Somatosensory Cortex  Anna Devor, Andrew K. Dunn, Mark L. Andermann, Istvan Ulbert, David A. Boas, Anders M. Dale  Neuron  Volume 39, Issue 2, Pages 353-359 (July 2003) DOI: 10.1016/S0896-6273(03)00403-3

Figure 1 Multiwavelength Imaging of Intrinsic Signals (A) Ratio images of activation for each of the 6 filters (wavelengths indicated above) were calculated by dividing the response (averaged 1.5–2.5 s following the stimulus) by the baseline image (averaged from 7 s preceding the stimulus). 990 trials were averaged for each stimulus amplitude. The signal is expressed in percent change from the baseline. Scale bar equals 500 μm. (B) Signal time course for each of the 9 stimulus amplitudes, calculated by averaging the signal from the ROI (square in A, first panel). Responses for each of the 6 filters are superimposed. The stimulus onset is denoted by an arrow. Legend: 560 nm (dark blue), 570 nm (light green), 580 nm (purple), 590 nm (light blue), 600 nm (red), 610 nm (dark green). Vertical scale bar equals 0.2%. Neuron 2003 39, 353-359DOI: (10.1016/S0896-6273(03)00403-3)

Figure 2 Spatial-Temporal Evolution of HbO, Hb, and HbT Each image represents an individual frame (average of 990 trials). Time between consecutive images is 200 ms. (B) is a continuation of the time series shown in (A). The signal for Hb and HbO is expressed in percent change relative to its own baseline concentration (40 and 60 μM, respectively). HbT was calculated as a sum of Hb and HbO. Scale bar equals 500 μm. Neuron 2003 39, 353-359DOI: (10.1016/S0896-6273(03)00403-3)

Figure 3 Simultaneous Recordings of Neural and Hemodynamic Signals (A) MUA (expressed in spikes per second) and LFP (expressed in units of SD compared to the baseline) as a function of poststimulus time and amplitude (1–9). (B) Signal time courses of Hb, HbO, and HbT calculated from the data in Figure 1B. Note that the Hb scale is inverted. Neuron 2003 39, 353-359DOI: (10.1016/S0896-6273(03)00403-3)

Figure 4 Saturation of Electrophysiological Measures Each point is an average of 990 stimulus trials. Average responses were normalized to the maximal amplitude. (A and B) MUA (A) and LFP (B) consistently saturate as a function of stimulus intensity. Responses for each of the 5 animals are superimposed. (C and D) MUA and LFP saturate for both the transient and the delayed response components. The responses shown in Figure 3 were integrated 0–25 ms (red), 25–300 ms (green), and 0–300 ms (blue) following the stimulus. (E and F) Averaged, rectifyed MUA (E) and CSD (F) recorded from supragranular layers (depth of 0–400 μm, red), granular layer (500–900 μm, blue), and infragranular layers (900–2000 μm, green). Neuron 2003 39, 353-359DOI: (10.1016/S0896-6273(03)00403-3)

Figure 5 Nonlinearity of Neurovascular Coupling Each point is an average of 4950 stimulus trials from 5 animals. Before averaging animals, ΣMUA, ΣLFP, Hb, HbO, and HbT responses to amplitude 9 was normalized to 1. The error bars represent intersubject standard error. (A and B) ΣMUA (A) and ΣLFP (B) plotted as a function of stimulus intensity. (C) ΣLFP as a function of ΣMUA. (D) Hb (blue), HbO (red), and HbT (black) peak responses increase linearly with stimulus intensity. (E) ΣLFP (right) and ΣMUA (left) as a function of the peak percent change in HbO (red) and HbT (black). A power-law function f = axb was fit to the data (solid lines). Note that the hemodynamic response continues to grow beyond the plateau in ΣLFP and ΣMUA. Neuron 2003 39, 353-359DOI: (10.1016/S0896-6273(03)00403-3)