Acute cognitive effects of high doses of dextromethorphan relative to triazolam in humans.
Lawrence P Carter, Chad J Reissig, Matthew W Johnson, Margaret A Klinedinst, Roland R. Griffiths, Miriam Z Mintzer
Drug and Alcohol Dependence March 1, 2013 DOI: 10.1016/j.drugalcdep.2012.08.025 (opens in new tab)
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Study at a glance
AI-extracted from the abstract| Characteristics | Double-blind, ascending dose run-up design Peer reviewed |
|---|---|
| Sample size | 12 |
| Population | Healthy volunteers with histories of hallucinogen use |
| Interventions | Dextromethorphan Triazolam |
| Dose | DXM: 100, 200, 300, 400, 500, 600, 700, 800 mg/70 kg; Triazolam: 0.25, 0.5 mg/70 kg |
| Duration | Up to 6 hours after drug administration |
| Keywords | Dextromethorphan Cough suppressant Antitussive Otc medication Drug abuse Substance abuse Dxm abuse Recreational use High-dose use Drug misuse Cognitive impairment Cognitive effects Mental function Attention Memory Thinking Psychomotor effects Drug safety Safety margin Therapeutic window Pharmacology Drug research Otc safety |
| Citations | 28 |
| Key points | Acute cognitive impairments from DXM occurred only at doses 10–30 times the therapeutic dose, but supratherapeutic doses impaired all cognitive tasks examined. |
Abstract
Although concerns surrounding high-dose dextromethorphan (DXM) abuse have recently increased, few studies have examined the acute cognitive effects of high doses of DXM. The aim of this study was to compare the cognitive effects of DXM with those of triazolam and placebo. Single, acute, oral doses of DXM (100, 200, 300, 400, 500, 600, 700, 800 mg/70 kg), triazolam (0.25, 0.5mg/70 kg), and placebo were administered p.o. to twelve healthy volunteers with histories of hallucinogen use, under double-blind conditions, using an ascending dose run-up design. Effects on cognitive performance were examined at baseline and after drug administration for up to 6h. Both triazolam and DXM produced acute impairments in attention, working memory, episodic memory, and metacognition. Impairments observed following doses of 100-300 mg/70 kg DXM were generally smaller in magnitude than those observed after 0.5mg/70 kg triazolam. Doses of DXM that impaired performance to the same extent as triazolam were in excess of 10-30 times the therapeutic dose of DXM. The magnitude of the doses required for these effects and the absence of effects on some tasks within the 100-300 mg/70 kg dose range of DXM, speak to the relatively broad therapeutic window of over-the-counter DXM preparations when used appropriately. However, the administration of supratherapeutic doses of DXM resulted in acute cognitive impairments on all tasks that were examined. These findings are likely relevant to cases of high-dose DXM abuse.
Citations in the library
Cited by 7
- Clinical applications of hallucinogens: A review. Experimental and Clinical Psychopharmacology August 1, 2016
- Double-blind comparison of the two hallucinogens psilocybin and dextromethorphan: similarities and differences in subjective experiences. Psychopharmacology February 1, 2018
- Double-blind comparison of the two hallucinogens psilocybin and dextromethorphan: effects on cognition. Psychopharmacology October 1, 2018
- Dextromethorphan Beyond the Cough: Exploring Its Psychedelic Potential: A Systematic Review CNS Drugs June 15, 2026
- Classics in Chemical Neuroscience: Dextromethorphan (DXM). ACS Chemical Neuroscience June 21, 2023
and 2 more in the library
Cites 6
- High doses of dextromethorphan, an NMDA antagonist, produce effects similar to classic hallucinogens. Psychopharmacology September 1, 2012
- Cognitive and subjective acute dose effects of intramuscular ketamine in healthy adults. Experimental and Clinical Psychopharmacology November 1, 2006
- Cognitive effects of intramuscular ketamine and oral triazolam in healthy volunteers. Psychopharmacology March 1, 2013
- Dextromethorphan abuse: clinical effects and management. Journal of the American Pharmacists Association 2009
- Short and long term changes in NMDA receptor binding in mouse brain following chronic phencyclidine treatment. Journal of Neural Transmission 2007
and 1 more in the library