Participants were assessed on three separate testing days, during which they were screened for in- and exclusion criteria, underwent a magnetic resonance imaging (MRI) scan (see below), and completed measures of social defeat and an [18F]-FDOPA PET/CT-scan. All participants signed informed consent prior to the start of the study. The study was approved by the medical ethics committee of Leiden University Medical Center (reference NL54244.058.15), and pre-registered within the Netherlands Trial Register (registration number NL6207, https://www.trialregister.nl/trial/6207).

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