Cited by 31Cannabis and Cannabinoid ResearchSubstance Abuse Treatment and OutcomesSmoking Behavior and Cessation

Guanfacine decreases symptoms of cannabis withdrawal in daily cannabis smokers

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Haney, Margaret, Cooper, Ziva D., Bedi, Gillinder, Herrmann, Evan, Comer, Sandra D., Reed, Stephanie Collins, Foltin, Richard W., Levin, Frances R.·2019·Addiction Biology

Abstract

The α2a‐adrenergic agonist, lofexidine, reduced cannabis withdrawal‐related sleep disruption in the laboratory, but side effects (e.g. fatigue, hypotension) limit its utility as a treatment for cannabis use disorder. This study tested the potential efficacy and tolerability of a daily bedtime administration of the FDA‐approved α2a‐adrenergic agonist, guanfacine, in a human laboratory model of cannabis use disorder. Daily, nontreatment‐seeking cannabis smokers (13M, 2F) completed a within‐subject study comprising two 9‐day inpatient study phases. Each phase tested the effects of daily placebo or immediate‐release guanfacine (2 mg) on cannabis intoxication (5.6 percent THC; 2 days), withdrawal (4 days of abstinence) and subsequent ‘relapse’ (3 days of cannabis self‐administration). Ratings of mood, sleep, cardiovascular effects, food intake, psychomotor performance and cannabis self‐administration were assessed. An outpatient phase preceded each inpatient phase for medication clearance or dose induction. Under placebo medication conditions, cannabis abstinence produced significant withdrawal, including irritability, sleep disruption and anorexia. Guanfacine reduced ratings of irritability and improved objective measures of sleep during cannabis withdrawal relative to placebo but did not reduce cannabis self‐administration. Guanfacine was well tolerated with little evidence of fatigue and only small decreases in blood pressure: no dose was held due to hypotension. Thus, a single daily administration of guanfacine at bedtime improved sleep and mood during cannabis withdrawal relative to placebo. This positive signal supports further studies varying the guanfacine dose, formulation or frequency of administration, or combining it with other medications to increase the likelihood of having an impact on cannabis use.

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Authors
Haney, M., Cooper, Z. D., Bedi, G., Herrmann, E., Comer, S. D., Reed, S. C., Foltin, R. W., & Levin, F. R.
Affiliations
  • Columbia University Irving Medical Center (US)
  • Division on Substance Use Disorders, New York State Psychiatric Institute and Department of Psychiatry Columbia University Medical Center New York NY USA
Corresponding author
Haney, Margaret
Venue
Addiction Biology
Publisher
Wiley
Published
2018-04-16
Volume
24
Issue
4
Pages
707-716
ISSN
  • 1355-6215 (ISSN-L)
  • 1369-1600
OpenAlex
W2802568925
Cited by
31
References
48
Citations by year
2026: 5 · 2025: 3 · 2024: 4 · 2023: 2 · 2022: 2 · 2021: 5 · 2020: 5 · 2019: 3 · 2018: 2
FWCI
2.42
Type
journal article
Language
en
Open access
Locations
  • Addiction Biology (publishedVersion)
  • PubMed (publishedVersion)
  • PubMed Central (acceptedVersion)
  • Minerva Access (University of Melbourne) (submittedVersion)
Funders
US National Institute on Drug Abuse (5U54DA037842)
Topics
  • Health Sciences › Medicine › Pharmacology › Cannabis and Cannabinoid Research
  • Health Sciences › Medicine › Epidemiology › Substance Abuse Treatment and Outcomes
  • Health Sciences › Medicine › Physiology › Smoking Behavior and Cessation
Keywords
guanfacine, cannabis withdrawal, cannabis use disorder, sleep disruption, irritability, relapse, hypotension, tolerability
MeSH terms
Adult, Affect, Anorexia, Blood Pressure, Cannabis, Marijuana Abuse, Feeding Behavior, Female, Humans, Irritable Mood, Male, Psychomotor Performance, Self Administration, Sleep, Substance Withdrawal Syndrome, Guanfacine, Young Adult, Adrenergic alpha-2 Receptor Agonists

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