sharon sanders
Editor-in-Chief & President
Positive moods allow us greater interaction with our environment. Negative moods tend to give us "tunnel" vision.
[SIZE=-1]Behavioral/Systems/Cognitive[/SIZE]
[SIZE=+2] Opposing Influences of Affective State Valence on Visual Cortical Encoding[/SIZE]
<nobr>Taylor W. Schmitz,<sup>1</sup><sup>,2</sup></nobr> <nobr>Eve De Rosa,<sup>1</sup><sup>,2</sup><sup>,3</sup></nobr> and <nobr>Adam K. Anderson<sup>1</sup><sup>,2</sup><sup>,3</sup></nobr>
<sup>1</sup>Department of Psychology, <sup>2</sup>University of Toronto Neuroscience Program, and <sup>3</sup>Rotman Research Institute, University of Toronto, Toronto, Ontario M5S 3G3, Canada
<!-- null --> Correspondence should be addressed to Taylor W. Schmitz, Department of Psychology, University of Toronto, 100 St. George Street, Toronto, ON M5S 3G3, Canada. Email: taylor@aclab.ca<script type="text/javascript"><!-- var u = "taylor", d = "aclab.ca"; document.getElementById("em0").innerHTML = '<a href="mailto:' + u + '@' + d + '">' + u + '@' + d + '<\/a>'//--></script>
<!-- ABS --> Positive and negative emotional states are thought to have originated<sup> </sup>from fundamentally opposing approach and avoidance behaviors.<sup> </sup>Furthermore, affective valence has been hypothesized to exert<sup> </sup>opposing biases in cognitive control. Here we examined with<sup> </sup>functional magnetic resonance imaging whether the opposing influences<sup> </sup>of positive and negative states extend to perceptual encoding<sup> </sup>in the visual cortices. Based on prior behavioral research,<sup> </sup>we hypothesized that positive states would broaden and negative<sup> </sup>states would narrow visual field of view (FOV). Positive, neutral,<sup> </sup>and negative states were induced on alternating blocks. To index<sup> </sup>FOV, observers then viewed brief presentations (300 ms) of face/place<sup> </sup>concentric center/surround stimuli on interleaved blocks. Central<sup> </sup>faces were attended, rendering the place surrounds unattended.<sup> </sup>As face and place information was presented at different visual<sup> </sup>eccentricities, our physiological metric of FOV was a valence-dependent<sup> </sup>modulation of place processing in the parahippocampal place<sup> </sup>area (PPA). Consistent with our hypotheses, positive affective<sup> </sup>states increased and negative states decreased PPA response<sup> </sup>to novel places as well as adaptation to repeated places. Individual<sup> </sup>differences in self-reported positive and negative affect correlated<sup> </sup>inversely with PPA encoding of peripheral places, as well as<sup> </sup>with activation in the mesocortical prefrontal cortex and amygdala.
<sup> </sup>Psychophysiological interaction analyses further demonstrated<sup> </sup>that valence-dependent responses in the PPA arose from opponent<sup> </sup>coupling with extrafoveal regions of the primary visual cortex<sup> </sup>during positive and negative states. These findings collectively<sup> </sup>suggest that affective valence differentially biases gating<sup> </sup>of early visual inputs, fundamentally altering the scope of<sup> </sup>perceptual encoding.
[SIZE=-1]Behavioral/Systems/Cognitive[/SIZE]
[SIZE=+2] Opposing Influences of Affective State Valence on Visual Cortical Encoding[/SIZE]
<nobr>Taylor W. Schmitz,<sup>1</sup><sup>,2</sup></nobr> <nobr>Eve De Rosa,<sup>1</sup><sup>,2</sup><sup>,3</sup></nobr> and <nobr>Adam K. Anderson<sup>1</sup><sup>,2</sup><sup>,3</sup></nobr>
<sup>1</sup>Department of Psychology, <sup>2</sup>University of Toronto Neuroscience Program, and <sup>3</sup>Rotman Research Institute, University of Toronto, Toronto, Ontario M5S 3G3, Canada
<!-- null --> Correspondence should be addressed to Taylor W. Schmitz, Department of Psychology, University of Toronto, 100 St. George Street, Toronto, ON M5S 3G3, Canada. Email: taylor@aclab.ca<script type="text/javascript"><!-- var u = "taylor", d = "aclab.ca"; document.getElementById("em0").innerHTML = '<a href="mailto:' + u + '@' + d + '">' + u + '@' + d + '<\/a>'//--></script>
<!-- ABS --> Positive and negative emotional states are thought to have originated<sup> </sup>from fundamentally opposing approach and avoidance behaviors.<sup> </sup>Furthermore, affective valence has been hypothesized to exert<sup> </sup>opposing biases in cognitive control. Here we examined with<sup> </sup>functional magnetic resonance imaging whether the opposing influences<sup> </sup>of positive and negative states extend to perceptual encoding<sup> </sup>in the visual cortices. Based on prior behavioral research,<sup> </sup>we hypothesized that positive states would broaden and negative<sup> </sup>states would narrow visual field of view (FOV). Positive, neutral,<sup> </sup>and negative states were induced on alternating blocks. To index<sup> </sup>FOV, observers then viewed brief presentations (300 ms) of face/place<sup> </sup>concentric center/surround stimuli on interleaved blocks. Central<sup> </sup>faces were attended, rendering the place surrounds unattended.<sup> </sup>As face and place information was presented at different visual<sup> </sup>eccentricities, our physiological metric of FOV was a valence-dependent<sup> </sup>modulation of place processing in the parahippocampal place<sup> </sup>area (PPA). Consistent with our hypotheses, positive affective<sup> </sup>states increased and negative states decreased PPA response<sup> </sup>to novel places as well as adaptation to repeated places. Individual<sup> </sup>differences in self-reported positive and negative affect correlated<sup> </sup>inversely with PPA encoding of peripheral places, as well as<sup> </sup>with activation in the mesocortical prefrontal cortex and amygdala.
<sup> </sup>Psychophysiological interaction analyses further demonstrated<sup> </sup>that valence-dependent responses in the PPA arose from opponent<sup> </sup>coupling with extrafoveal regions of the primary visual cortex<sup> </sup>during positive and negative states. These findings collectively<sup> </sup>suggest that affective valence differentially biases gating<sup> </sup>of early visual inputs, fundamentally altering the scope of<sup> </sup>perceptual encoding.