Figure 1.
Schematic diagram of experimental design and procedure.
After EEG preparation (top row), participants were randomly assigned to sitting or bed rest position (control and experimental group, respectively; second row). Two surface gold electrodes were applied on the internal left wrist and participants' electric pain threshold was computed by means of a 10-point visuo-analogue scale representing different levels of pain intensity (third row). Participants started the experimental task which consisted in the EEG recording and subjective pain evaluations during pseudo-random administration of four different levels of electrical intensities (bottom row).
Figure 2.
Group-level grand-average waveforms of selected electrodes (in correspondence of the somatosensory cortex) showing the time-course of somatosensory processing (top row) during Control and Under Threshold conditions (left and right panel, respectively), and pain processing (bottom row) during Threshold and Over Threshold conditions (left and right panel, respectively) in sitting controls (blue line) and Bed Rest participants (red line).
Negativity is displayed upward. Spline interpolated maps of potentials representing scalp top views of P2 component (190–220 ms) in the four different conditions are depicted in blue and red boxes for control and Bed Rest groups, respectively.
Figure 3.
Analysis of P1 component during the 40- to 50-ms epoch after electrical stimuli: significant three-way Group by Stimulus Intensity by Laterality interaction.
Mean activity and Standard Error (SE) are depicted for Control (blue bars) and Bed Rest group (red bars). Control group (blue line) showed greater positivity on right vs. left clusters of electrodes (contralateral to the side of stimulation) for Under Threshold, Threshold and Over Threshold intensities, whereas BR group (red dotted line) revealed no difference among the four stimulus conditions.
Figure 4.
Analysis of N1 component during the 80- to 90-ms epoch after electrical stimuli: significant three-way Group by Stimulus Intensity by Laterality interaction.
Mean activity and Standard Error (SE) are depicted for Control (blue bars) and Bed Rest group (red bars). During Under Threshold and Threshold intensities, control group (blue line) showed greater negativity on lateral right vs. medial left clusters of electrodes, whereas BR group (red dotted line) exhibited greater negativity on medial right vs. both left clusters. During Over Threshold condition, controls showed greater negativity in right clusters vs. medial left sites, and greater negativity than BR participants in the lateral right cluster. No between-group differences have been found in the control condition.
Figure 5.
Analysis of P2 component during the 190- to 220-ms interval after electrical pulse: significant three-way Group by Stimulus Intensity by Laterality interaction.
Mean activity and Standard Error (SE) are depicted for Control (blue bars) and Bed Rest group (red bars). With the exception of Control condition, both groups exhibited greater positivity in medial vs. lateral locations of both hemispheres, showing the typical, inverted U-shape pattern. Compared with BR participants (red dotted line), controls exhibited greater positivity in medial left clusters for Threshold and Over Threshold conditions (blue line).
Figure 6.
Source localization computed with sLORETA for Under and Over Threshold conditions (left and right column, respectively) for control and BR groups during P1 (first and second row, respectively), N1 (third and fourth row, respectively) and P2 components (fifth and sixth row, respectively).
In the first and third columns are depicted the top views of source analyses, in the second and forth ones the midsagittal views.
Table 1.
Source analyses of the first positive component P1 (40–50 ms) in controls and BR participants.
Table 2.
Source analyses of the first negative component N1 (80–90 ms) in controls and BR participants.
Table 3.
Source analyses of the second positive component P2 (190–220 ms) in controls and BR participants.