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Title: Spontaneous and instructed regulation of negative emotion


1
Spontaneous and instructed regulation of negative
emotion Brent L. Hughes, Tor D. Wager, Matthew L.
Davidson, and Kevin N. Ochsner Department of
Psychology, Columbia University
324 Schermerhorn Hall Department of
Psychology 1190 Amsterdam Ave. New York, NY 10027
Download this poster http//www.columbia.edu/cu/p
sychology/tor/
RESULTS fMRI ACTIVITY
RESULTS REPORTED AFFECT
INTRODUCTION
  • BACKGROUND
  • The capacity to adaptively regulate emotion
    is essential for both mental and physical
    health
  • Recent imaging research has identified
    regions of PFC important for the goal-directed,
    deliberate, voluntary reappraisal of aversive
    stimuli (Beauregard et al., 2001 Ochsner et al.,
    2002 Phan et al., 2004 Urry et al., 2006)
  • Behavioral research (Erber, 1996) suggests
    that individuals also spontaneously regulate
    their emotion when faced with aversive
    situations, even when not explicitly directed to
    do so, but there are no brain-based studies of
    this.
  • QUESTION
  • In this study, we sought to identify common
    and distinct regions
  • involved in the spontaneous and instructed
    regulation of emotion

Regions Involved in Spontaneous Regulation
Regions Involved in Instructed Regulation
Look Neg lt Look Neu BOLD
Figure 6. Ratings of negative affect showed that
reappraisal decreased negative affect reported in
response to photos.
SUMMARY and CONCLUSIONS
METHODS
  • The Look Neg gt Look Neutral comparison showed
    increases in frontal, parietal, and insular
    cortices, amygdala, nucleus accumbens (NACC), and
    brainstem, and decreases in ventromedial frontal
    cortex, superior temporal cortices, and
    mid-cingulate. 
  • Conjunction analyses revealed regions whose
    activity correlated with reduced affect,
    including the anterior insula/opercular junction,
    hippocampus, midbrain, Right IFG, DMPFC, dACC,
    and cerebellum. These regions may play roles in
    the appraisal process and/or internally guided
    interpretations of aversive pictures. Decreases
    in VMPFC and superior temporal cortex may relate
    to differences in the self-relevance of pictures,
    cognitive activity, or affective experience.
  • To further constrain this hypothesis, we
    compared Look Neg activity with activity elicited
    by the voluntary reappraisal of negative affect. 
    Compared with viewing negative images,
    reappraising them (Reapp Neg gt Look Neg) further
    increased activity in a number of similar sites,
    including lateral and medial frontal cortices,
    ventral striatum, and thalamus.  Decreases were
    found in amygdala, parahippocampal cortex, and
    STS. Frontal activity was most strongly
    correlated with changes in affect reports. 
  • DMPFC and right IFG showed activations and
    correlations with reduced affect reports in both
    free-viewing and instructed conditions. These
    regions are candidate regions for voluntary
    context-based control of appraisal.
  • PARTICIPANTS
  • n 36 participants, mean age 22 years
  • SCAN ANALYSIS PARAMETERS
  • EPI BOLD imaging on 1.5T GE (TR 2 s, 31 slices
    3.5 x 3.5 x 4.5 mm voxels).
  • Pre-processing and 1st level analysis with SPM2
  • 2nd-level analysis using robust regression to
    down-weight outliers (Wager et al., 2005)
  • STIMULI
  • Negative and neutral IAPS images
  • TRIAL TYPES
  • Reappraise Negative Images Instructed
    regulation
  • Look at Negative Images Spontaneous
    responses, which could
  • include regulation of emotion
  • Look at Neutral Images Spontaneous responses
    to neutral events
  • TRIAL STRUCTURE

2
2
1
1
Figure 4. Reapp Neg gt Look Neg Intersection with
Covariate (activation at p lt .05 FDR corrected (p
lt .004), AND correlated with reduced affect p lt
0.05)
Positive positive correlation with reductions
in affect
Positive positive correlation with reductions
in affect
Common Regions for Spontaneous and Instructed
Regulation
REFERENCES
  • ANALYSIS PATHWAY
  • Step 1 Used contrasts to identify regions (P lt
    .05 FDR) involved in
  • 1. Spontaneous responses to images (Look Neg gt
    Look Neu)
  • 2. Instructed reappraisal (Reapp Neg gt Look Neg)
  • Step 2 Used whole brain regression analyses with
    self-reported affect as a covariate to
    identify regions
  • Whose activation predicts drops in negative
    affect when Looking at Negative Images
  • Whose activation predicts drops in negative
    affect during Reappraisal
  • Step 3 Identified intersection of Steps 1 and 2
    (activated AND correlated).
  • Step 4 Identified regions involved in both
    spontaneous and instructed regulation (P lt .1 FDR
    activation and p lt .05 correlation in 1 AND 2)
  • (see Nichols et al., 2005 for details on
    conjunction analysis methods.)

Beauregard, M, Levesque, J, Bourgouin, P. (2001).
Neural Correlates of Conscious Self-Regulation
of Emotion. Journal of Neuroscience, 21 RC165
1-6. Erber, R. (1996). The self-regulation of
moods. In L. L. Martin A.Tesser (Eds.),
Striving and feeling Interactions among goals,
affect,and self- regulation (pp.
251-275). Harenski, CL, Hamann, S. (2006).
Neural correlates of regulating negative
emotions related to moral violations.
NeuroImage, 30 (1), 313-324. Nichols, T., Brett,
M., Andersson, J., Wager, T., Poline, J. B.
(2005). Valid conjunction inference with the
minimum statistic. Neuroimage, 25(3),
653-660. Ochsner, K. N., Bunge, S. A., Gross, J.
J., Gabrieli, J. D. E. (2002). Rethinking
feelings An fMRI study of the cognitive
regulation of emotion. Journal of Cognitive
Neuroscience, 148. Phan, K. L., Fitzgerald, D.
A., Nathan, P. J., Moore, G. J., Uhde, T. W.,
Tancer, M. E. (2005). Neural substrates for
voluntary suppression of negative affect A
functional magnetic resonance imaging study.
Biol Psychiatry, 57(3), 210-219. Urry, H. L.,
van Reekum, C. M., Johnstone, T., Kalin, N. H.,
Thurow, M.E., Schaefer, H. S., et al. (2006).
Amygdala and ventromedial prefrontal cortex are
inversely coupled during regulation of negative
affect and predict the diurnal pattern of
cortisol secretion among older adults.
JNeurosci, 26(16), 4415-4425. Wager, T. D.,
Keller, M. C., Lacey, S. C., Jonides, J.
(2005). Increased sensitivity in neuroimaging
analyses using robust regression. NeuroImage,
26(1), 99-113. Wager, T. D., Phan, K. L.,
Liberzon, I., Taylor, S. F. (2003). Valence,
gender, and lateralization of functional brain
anatomy in emotion A meta-analysis of findings
from neuroimaging. Neuroimage, 19, 513-531.
Reapp Neg gt Look Neg BOLD
Look Neg lt Look Neu BOLD
Temporal/ Occipital Cortex
R IFG
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