Serotonergic Modulation of Intrinsic Functional Connectivity

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Serotonergic Modulation of Intrinsic Functional Connectivity Alexander Schaefer, Inga Burmann, Ralf Regenthal, Katrin Arélin, Claudia Barth, André Pampel, Arno Villringer, Daniel S. Margulies, Julia Sacher  Current Biology  Volume 24, Issue 19, Pages 2314-2318 (October 2014) DOI: 10.1016/j.cub.2014.08.024 Copyright © 2014 Elsevier Ltd Terms and Conditions

Figure 1 Study Design Twenty-two subjects underwent three resting-state scanning sessions: after a baseline rs-MRI scan, participants received either a single oral dose of the study drug escitalopram (20 mg) (depicted by a red star) or placebo (depicted by a green rectangle) in a randomized design. Serum levels of escitalopram were determined after 3 hr followed by a second rs-fMRI scan. After a wash-out period of 8 weeks, the protocol was repeated with the alternate study drug (escitalopram or placebo) to adhere to a double-blind intraindividual design. rs-fMRI scans are indicated as blue circles. Current Biology 2014 24, 2314-2318DOI: (10.1016/j.cub.2014.08.024) Copyright © 2014 Elsevier Ltd Terms and Conditions

Figure 2 Comparison of Average Degree Centrality Baseline versus Placebo and Escitalopram Sagittal slices of mean degree centrality of three conditions: (A) baseline, (B) placebo, and (C) escitalopram (20 mg), superimposed on a T1-anatomical standard template. Orange colors indicate higher centrality. Baseline and placebo condition show more similar centrality patterns, whereas degree centrality analysis reveals a global signal change following the administration of the SSRI. Current Biology 2014 24, 2314-2318DOI: (10.1016/j.cub.2014.08.024) Copyright © 2014 Elsevier Ltd Terms and Conditions

Figure 3 Signal Change in Degree Centrality Induced by a Single Dose of Escitalopram Contrasted with Placebo Sagittal slices show the contrast of degree centrality between placebo and escitalopram condition superimposed on a T1-anatomical standard MNI template. Orange colors indicate increased centrality; blue colors decreased centrality following SSRI administration compared to placebo. Dark lines indicate significant clusters (p < 0.01, corrected for multiple comparisons). Significant increases in degree centrality are located in the thalamus and the cerebellum; decreases in degree centrality were found throughout the neocortex. Position of sagittal slices is shown in one axial slice. Table S1 provides a comprehensive overview of all significant clusters in the escitalopram versus placebo condition. Figure S3 depicts the contrast at a range of thresholds (r > 0.10, r > 0.15, r > 0.20). Current Biology 2014 24, 2314-2318DOI: (10.1016/j.cub.2014.08.024) Copyright © 2014 Elsevier Ltd Terms and Conditions

Figure 4 Change of Functional Connectivity between the Placebo and SSRI Condition and Euclidean Length of Connection The x axis indicates the Euclidean distance (mm) between the two endpoints of the respective connection. The y axis displays the mean functional connectivity difference (placebo-SSRI). The color indicates the number of connections, with hot colors reflecting a high number of connections with specific distance and change and blue colors indicating fewer connections. For further details on connectivity changes within and between network modules, see Figures S1 and S2. Current Biology 2014 24, 2314-2318DOI: (10.1016/j.cub.2014.08.024) Copyright © 2014 Elsevier Ltd Terms and Conditions