21 research outputs found

    Areas of sensitization and stimulation on the right lateral volar forearm.

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    <p>For orientation, the schematic drawing on the left shows a dermatome map of the right upper extremity (redrawn and modified from <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0112325#pone.0112325-Trepel1" target="_blank">[20]</a>). The area of testing (marked by the circle) is situated on the right lateral volar forearm in the C6 dermatome. <i>Area A:</i> Site of sensitization with the heat/capsaicin model (3×3 cm square area 3 cm distal to the elbow in the C6 dermatome). <i>Area B:</i> Site of mechanical stimulation corresponding to the area of secondary mechanical hyperalgesia (2×5 cm area distal to area A).</p

    Spinal group activation patterns before (left column) and after (middle column) sensitization and contrast maps (right column).

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    <p>The transverse slices are in radiological orientation with the left side corresponding to the right body side and approximate the corresponding spinal cord segment for a rostral-caudal span from C4 to T1. They show spinal regions of signal intensity change before (left column) and after (middle column) sensitization with the heat/capsaicin model representing the significance (T-value) of each active voxel across the 16 subjects. The right column shows partial-least squares (PLS) results of contrast calculations on a voxel-by-voxel basis. The color bar in <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0112325#pone-0112325-g003" target="_blank">figure 3</a> indicates the corresponding significance, i.e. T-value (left and middle column) or bootstrap-ratio (right column) for each color. <i>Left Column:</i> Activations in ipsilateral vGM of C4. Deactivations in bilateral deep dGM of C6 and C8 and contralateral deep dGM of C7. <i>Middle column:</i> Ipsilateral activations in superficial dGM of T1 and vGM of C4. Deactivations in ipsilateral superficial dGM of C7. <i>Right column:</i> Activations in ipsilateral superficial dGM (C7, C8) and in contralateral vGM (C7) and deep dGM (C8). Deactivations in ipsilateral vGM and contralateral dGM of C4.</p

    Psychophysical data.

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    <p>(A) Mean ratings of pain intensity (dashed line) and temperature perception (solid line) during capsaicin application. Capsaicin was applied at time 0. Mean ± standard error of the mean (SEM). (B) Mean pain ratings for the mechanical stimulus before and after application of capsaicin. Capsaicin induced secondary mechanical hyperalgesia. Mean ± SEM. *: p<0.05.</p

    Sagittal slices of group activation patterns and contrast maps.

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    <p>Columns 1 to 4 show areas of activity across brain stem and cervical spinal cord before (1<sup>st</sup> and 2<sup>nd</sup> column) and after (3<sup>rd</sup> and 4<sup>th</sup> column) sensitization with the heat capsaicin model representing the significance (T-value) of each active voxel across the 16 subjects. Columns 5 and 6 show partial-least squares (PLS) results of contrast calculations on a voxel-by-voxel basis. The left column of each 2 columns (e.g. 1<sup>st</sup>, 3<sup>rd</sup> and 5<sup>th</sup>) corresponds to the ipsilateral side of the stimulus, the right column to the contralateral side. The color bar on the right indicates the corresponding significance, i.e. T-value (columns 1–4) or bootstrap-ratio (columns 5–6) for each color.</p

    Time course of tumor development after intracerebral injection of 10,000 C6-glioma cells.

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    <p>T2-weighted images (T2w) revealed an increase in tumor mass over time which was accompanied by an increasing area of contrast enhancement (G1-T1w). At day 9 maps of percentage of signal recovery (PSR) and signal recovery (SR) indicated a higher capillary permeability in the tumor center (white ring) extending over time. Higher PSR and SR values were also seen in the region of the choroid plexus (open arrow). Higher cerebral blood volume (CBV) was mainly found at the tumor rim (white arrow and ring).</p

    Cerebral blood volume (CBV) and vessel density.

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    <p>The highest CBV was found at the rim of the tumor which also showed the highest vessel density (bar graph) as revealed by immunohistochemistry for von Willebrand factor (vWF, lower row): (left) overview showing the position of the magnified view of the tumor rim (orange box) and tumor center (green box), upper row, left: the corresponding axially oriented T2-weighted image.</p

    Spatial heterogeneity of cerebral blood volume (CBV) and signal recovery (SR).

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    <p>Maps of SR (purple) were overlaid on maps of CBV (green) obtained on day 21 after injection of 100,000 C6 cells. Areas of increased CBV were mostly found at the tumor rim whereas signal recovery exceeding the baseline was mainly seen in the tumor center excluding regions which were most likely necrotic (dark on T2 weighted images). Coronally and axially oriented T2-weighted images (T2w) are shown as reference.</p

    Robustness of signal recovery (SR) and percentage of signal recovery (PSR) maps.

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    <p>In case of alteration of the bolus peak PSR maps became unusable, while SR still provided exploitable results. On the right the corresponding axially oriented T2-weighted image.</p
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