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Gamma-hydroxybutyrate enhances mood and prosocial behavior without affecting plasma oxytocin and testosterone

Oliver G. Bosch, Christoph Eisenegger, Jürg Gertsch, Robin von Rotz, Dario Dornbierer, M. Salomé Gachet, Markus Heinrichs, Thomas C. Wetter, Erich Seifritz, Boris B. Quednow

Psychoneuroendocrinology July 17, 2015 DOI: 10.1016/j.psyneuen.2015.07.167 (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics Randomized, placebo-controlled, cross-over design Peer reviewed
Sample size 16
Population Healthy males
Intervention Gamma-hydroxybutyrate (GHB)
Dose 20 mg/kg
Measures visual-analogue-scales, GHB-Specific-Questionnaire, Charity Donation Task, Social Value Orientation test, Reciprocity Task
Keywords Prosocial behavior Adrenocorticotropic hormone Testosterone patch Mood Oxytocin Endocrinology Empathy Empathic concern Euphoriant Clinical psychology Developmental psychology Perspective-taking
Citations 42
Key points GHB increased prosocial behavior in participants with low prosociality and elevated plasma progesterone, without affecting social hormones like oxytocin or testosterone.

Abstract

Gamma-hydroxybutyrate (GHB) is a GHB-/GABAB-receptor agonist. Reports from GHB abusers indicate euphoric, prosocial, and empathogenic effects of the drug. We measured the effects of GHB on mood, prosocial behavior, social and non-social cognition and assessed potential underlying neuroendocrine mechanisms. GHB (20mg/kg) was tested in 16 healthy males, using a randomized, placebo-controlled, cross-over design. Subjective effects on mood were assessed by visual-analogue-scales and the GHB-Specific-Questionnaire. Prosocial behavior was examined by the Charity Donation Task, the Social Value Orientation test, and the Reciprocity Task. Reaction time, memory, empathy, and theory-of-mind were also tested. Blood plasma levels of GHB, oxytocin, testosterone, progesterone, dehydroepiandrosterone (DHEA), cortisol, aldosterone, and adrenocorticotropic-hormone (ACTH) were determined. GHB showed stimulating and sedating effects, and elicited euphoria, disinhibition, and enhanced vitality. In participants with low prosociality, the drug increased donations and prosocial money distributions. In contrast, social cognitive abilities such as emotion recognition, empathy, and theory-of-mind, and basal cognitive functions were not affected. GHB increased plasma progesterone, while oxytocin and testosterone, cortisol, aldosterone, DHEA, and ACTH levels remained unaffected. GHB has mood-enhancing and prosocial effects without affecting social hormones such as oxytocin and testosterone. These data suggest a potential involvement of GHB-/GABAB-receptors and progesterone in mood and prosocial behavior.