Oxytocin vs. placebo effects on intrusive memory consolidation using a trauma film paradigm: a randomized, controlled experimental study in healthy women

Author:

Maslahati Tolou1,Wingenfeld Katja2ORCID,Hellmann-Regen Julian3ORCID,Kraft Julia,Lyu Jing,Keinert Marie,Voß Aline,Cho An Bin,Ripke Stephan4,Otte Christian5ORCID,Schultebraucks Katharina6ORCID,Roepke StefanORCID

Affiliation:

1. Charité - Universitätsmedizin Berlin

2. Charité University Berlin

3. Charité University Medicine Berlin, Corporate Member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health

4. Charite Universitaetsmedizin Berlin, Dept. of Psychiatry and Psychotherapy

5. Charite University Medical Center

6. Columbia University

Abstract

Abstract Oxytocin administration during a trauma analogue has been shown to increase intrusive memories, which are a core symptom of Post-Traumatic Stress Disorder (PTSD). However, it is unknown whether oxytocin influences the acquisition or the consolidation of the trauma. The current study investigates the effect of the activation of the oxytocin system during the consolidation of an analogue trauma on the formation of intrusive memories over four consecutive days and whether this effect is influenced by individual neurobiological, genetic, or psychological factors. We conducted a randomized double-blind placebo-controlled study in 217 healthy women. They received either a single dose of intranasal oxytocin (24 IU) or placebo after exposure to a trauma film paradigm, which reliably induces intrusive memories. We used a general random forest to examine a potential heterogeneous treatment effect of oxytocin on the consolidation of intrusive memories. Furthermore, we used a poisson regression to examine whether salivary alpha amylase activity (sAA) as a marker of noradrenergic activity and cortisol response to the film, polygenic risk score (PRS) for psychiatric disorders, and psychological factors influence the number of intrusive memories. We found no significant effect of oxytocin on the formation of intrusive memories (t(-0.85) = 201.72, p = 0.40, Cohen’s d = 0.12, 95% CI -0.02–0.26) and identified no heterogeneous treatment effect. We replicated previous associations of the PRS for PTSD, sAA and the cortisol response on intrusive memories. We further found a positive association between high trait anxiety and intrusive memories, and a negative association between the emotion regulation strategy reappraisal and intrusive memories. Data of the present study suggest that the consolidation of intrusive memories is modulated by genetic, neurobiological and psychological factors, but is not influenced by oxytocin. Trial registration: NCT03875391.

Publisher

Research Square Platform LLC

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