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Nitrous oxide speeds the reduction of distressing intrusive memories in an experimental model of psychological trauma

Ravi Das, Amanda J. F. Tamman, Viktoriya L. Nikolova, Tom P. Freeman, James A. Bisby, Antonio Ivan Lazzarino, Sunjeev K. Kamboj

Psychological Medicine March 3, 2016 DOI: 10.1017/s003329171600026x (opens in new tab) via OpenAlex

Summary

AI-generated from the abstract

Inhaling nitrous oxide shortly after a traumatic event speeds the decline of intrusive memories, reducing them by the next day compared to four days later with medical air. The gas appears to disrupt memory consolidation, but it increases intrusive memories in people who were highly dissociated at the time of the trauma. Sleep quality did not differ between groups. The findings suggest nitrous oxide may help prevent PTSD symptoms in some individuals, but caution is warranted for those with dissociation.

Study at a glance

Characteristics Randomized controlled trial Peer reviewed
Sample size 50
Population Healthy participants who viewed a negatively valenced emotional film clip
Interventions Nitrous oxide Medical air
Duration 1 week follow-up
Keywords Intrusion Recall Dissociative Audiology Memory consolidation
Citations 48
Key finding Nitrous oxide speeds the reduction of intrusive memory frequency after analogue trauma, but increases intrusion frequency in highly dissociated individuals.

Abstract

BACKGROUND: Post-traumatic stress disorder (PTSD) involves maladaptive long-term memory formation which underlies involuntary intrusive thoughts about the trauma. Preventing the development of such maladaptive memory is a key aim in preventing the development of PTSD. We examined whether the N-methyl d-aspartate receptor (NMDAR) antagonist gas nitrous oxide (N2O) could reduce the frequency of intrusive memories by inhibiting NMDAR-dependent memory consolidation in a laboratory analogue of psychological trauma. METHOD: Participants were randomized to inhale N2O (N = 25) or medical air (N = 25) after viewing a negatively valenced emotional film clip ('trauma film'). Participants subsequently completed a daily diary assessing frequency of intrusive thoughts relating to the film clip. A week later, participants completed an explicit memory recall task related to the film. RESULTS: Post-encoding N2O sped the reduction in intrusive memory frequency, with a significant reduction by the next day in the N2O group compared to 4 days later in the air group. N2O also interacted with post-film dissociation, producing increased intrusion frequency in those who were highly dissociated at baseline. Sleep length and quality the night after viewing the film did not differ between the groups. CONCLUSION: N2O speeds the reduction of intrusive analogue trauma memory in a time-dependent manner, consistent with sleep-dependent long-term consolidation disruption. Further research with this drug is warranted to determine its potential to inoculate against enduring effects of psychological trauma; however, caution is also urged in dissociated individuals where N2O may aggravate PTSD-like symptomatology.

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