Incidental affective states, i.e., affective states can influence decision making and selective attention to threatening information. Acute stress is such an affective state and is a powerful contextual modulator of decision-making processes and selective attention to threat. In terms of physiological and neurohormonal changes, the stress response has been well characterized: Exposure to stress elicits an array of autonomic, endocrine, and behavioral responses. The physiological stress response is mediated by the hypothalamic-pituitary-adrenal (HPA) axis and the locus coeruleus noradrenergic (LC-NA) system with cortisol and norepinephrine (NE) as their end products. There is compelling evidence that the stress hormones cortisol and NE influence cognitive processes. However, only very few studies so far used pharmacological approaches to specify the role of stress neuromodulators on decision making and selective attention to threat and these studies are hardly comparable due to differences in the experimental design, e.g., the decision making task used. Furthermore, the neural underpinnings of stress effects on decision making and selective attention to threat are uninvestigated so far. The aim of the proposed project is to clarify the role of the major stress neuromodulators, NE and cortisol, in their contribution to different processes related to decision making under risk and selective attention to threat. To this end, combined precise pharmacological stimulation, behavioral modeling, and fMRI methods will be applied to systematically disentangle the effects of stress hormones on risk attitudes and loss aversion as well as their relation to neural correlates of processing subjective value and risk. Using pharmacological manipulation, the influence of noradrenergic and glucocorticoid activity on decision making under risk at the behavioral, computational, and neural level will be investigated. In addition, the influence of noradrenergic and glucocorticoid activity on selective attention to threat at the behavioural and neural level using a dot-probe paradigm with fearful and neutral faces will be examined. Participants are randomly assigned to one of four groups: (A) yohimbine, (B) hydrocortisone, (C) yohimbine and hydrocortisone, or (D) placebo.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
DOUBLE
Enrollment
167
Effects on neural correlates of decision-making under risk and selective attention to threat
Effects on neural correlates of decision-making under risk and selective attention to threat
Effects on neural correlates of decision-making under risk and selective attention to threat
Effects on neural correlates of decision-making under risk and selective attention to threat
Charite University
Berlin, Germany
Risk and loss-aversion, choice consistency
Behavioural outcome of the decision-making under risk task modeled using prospect theory (PT)
Time frame: 45 minutes
Patch-leaving times
Behavioural outcome of the decision-making under risk task including a foraging task part using marginal value theory
Time frame: 45 minutes
Attentional bias to fearful faces
Behavioural outcome of the dot-probe task
Time frame: 12 minutes
Blood-oxygen-level-dependent (BOLD) response
In both tasks
Time frame: 45 + 12 minutes
Salivary cortisol
Treatment check
Time frame: 3 hours
Salivary alpha amylase
Treatment check
Time frame: 3 hours
Systolic and diastolic blood pressure
Treatment check
Time frame: 3 hours
Heart rate
Treatment check
Time frame: 3 hours
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