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Oxytocin Attenuates the Anxiety Response to Interpersonal Stress in Females High in Emotion-Oriented Coping


Poster

OXYTOCIN, INTRANASAL, INTERPERSONAL STRESS, ANXIETY, EMOTION-ORIENTED COPING, YALE INTERPERSONAL STRESSOR

Cardoso, Christopher; Linnen, Anne-Marie; Ellenbogen, Mark A.; Joober, Ridha

Centre for Research in Human Development, Concordia University, Montréal, Canada; Douglas Hospital Research Centre, McGill University, Montréal, Canada

Chronic interpersonal stress has been associated with the development of physical (Swaab, Bao, & Lucassen, 2005) and mental illness (Tull, Jakupak, & McFadden, 2007). Both biological and psychological factors appear to be implicated in the regulation of interpersonal stress. For example, emotion-oriented coping represents a maladaptive coping style that increases stress reactivity to interpersonal challenge (Ravindran, et al., 2002). Moreover, there is recent biological evidence to suggest that exogenously administered oxytocin attenuates the stress response to conflict among couples (Ditzen, et al., 2009). The aim of the present study was to examine the interaction between oxytocin and coping style on the mood response to an interpersonal stressor.

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Ninety-nine undergraduate students participated in the Yale Interpersonal Stressor (YIPS; Stroud et al., 2000), a live social rejection paradigm. Prior to the start of the YIPS, participants were administered either a single intranasal dose of oxytocin (24 I.U.) or placebo. Affect was measured via the Profile of Mood States (POMS), which was administered at four separate intervals throughout the paradigm. Coping style was measured using the Coping Inventory for Stressful Situations (CISS).


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Statistical analyses were conducted on the composed-anxiety scale of the POMS. A repeated measures analysis revealed a significant effect of mood across time (F (3, 95) = 27.63, p < .001, η2 = .22). Relative to baseline, participants reported a significant increase in anxiety in response to the YIPS. Among females, a significant interaction was obtained between emotion-oriented coping and drug condition (oxytocin, placebo; ΔR2 = .09, F(1, 46) = 4.63, p < .05). The administration of oxytocin was associated with a reduction in anxiety, relative to placebo, in females high in emotion-oriented coping.


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In the present study, oxytocin attenuated the anxiety response to the YIPS among females high in emotion-oriented coping. Considering that emotion-oriented coping is typically associated with heightened stress reactivity, our results indicate that oxytocin may be modulating this relationship.


Mr.

Christopher


Cardoso


Concordia University

Research Coordinator

BA Psychology


chriscardoso@live.ca

(514) 848-2424 xt:. 5456



Stress and Developmental Psychopathology Lab

Department of Psychology, Concordia University

7141 Sherbrooke St. West

Montreal

QC

H4B 1R6

Canada
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