A within-subject cross-over trial comparing the acute effects of vaporized delta-8-tetrahydrocannabinol and delta-9-tetrahydrocannabinol in healthy adults
The prevalence and accessibility of Δ8-tetrahydrocannabinol (Δ8-THC), a chemical isomer of Δ9-tetrahydrocannabinol (Δ9-THC), has increased drastically, yet no controlled studies have directly compared the effects of vaporized Δ8-THC and Δ9-THC . Twenty healthy adults with no past-month cannabis expo...
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Published in | Drug and alcohol dependence Vol. 272; p. 112684 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
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Elsevier B.V
01.07.2025
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ISSN | 0376-8716 1879-0046 1879-0046 |
DOI | 10.1016/j.drugalcdep.2025.112684 |
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Abstract | The prevalence and accessibility of Δ8-tetrahydrocannabinol (Δ8-THC), a chemical isomer of Δ9-tetrahydrocannabinol (Δ9-THC), has increased drastically, yet no controlled studies have directly compared the effects of vaporized Δ8-THC and Δ9-THC .
Twenty healthy adults with no past-month cannabis exposure completed five randomized outpatient sessions in a within-subjects, double-blind, crossover design. Participants inhaled Δ8-THC (10, 20, 40mg), Δ9-THC (20mg), or placebo (distilled water) using the Mighty Medic vaporizer. Measures included subjective drug effects, cognitive/psychomotor performance, puff topography, vital signs, and whole blood concentrations of Δ8-THC, Δ9-THC, and their metabolites.
All Δ8-THC doses and Δ9-THC produced subjective drug effects that differed from placebo. 20mg Δ9-THC elicited stronger ratings of “drug effect” and “unpleasant” than 10mg Δ8-THC; no other subjective effects differed between Δ8-THC and Δ9-THC. 20mg Δ9-THC impaired DRUID performance compared with placebo; no other significant differences were observed between conditions on cognitive/psychomotor measures. Few pharmacodynamic differences were observed between Δ8-THC doses. Evidence of compensatory puffing emerged, with longer/larger puffs at lower Δ8-THC doses and placebo. Blood cannabinoid concentrations revealed that Δ8-THC metabolism differed from Δ9-THC, with less psychoactive 11-OH metabolite formed after Δ8-THC exposure.
Various doses of vaporized Δ8-THC elicited comparable psychoactive effects as vaporized Δ9-THC, which is noteworthy considering Δ8-THC is less potent and generally perceived as less harmful/intoxicating than Δ9-THC. The magnitude of effects from cannabinoids is dictated by several factors including dose, route of administration, and, for inhaled methods, puffing behaviors. These data should be considered in future drug policy and public education initiatives.
•The prevalence of Δ8-tetrahydrocannabinol (Δ8-THC) has increased across the U.S.•Weevaluated the effects of vaporized Δ8-THC (10, 20, 40 mg) versus Δ9-THC (20mg) in healthy adults.•Vaporized Δ8-THC and Δ9-THC produced largely similar effects across all doses.•Participants altered their puffing behaviors based on Δ8-THC dose, indicative of titration.•Δ8-THC metabolism differed from Δ9-THC, as less psychoactive 11-OH metabolite was formed after Δ8-THC exposure |
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AbstractList | The prevalence and accessibility of Δ8-tetrahydrocannabinol (Δ8-THC), a chemical isomer of Δ9-tetrahydrocannabinol (Δ9-THC), has increased drastically, yet no controlled studies have directly compared the effects of vaporized Δ8-THC and Δ9-THC .
Twenty healthy adults with no past-month cannabis exposure completed five randomized outpatient sessions in a within-subjects, double-blind, crossover design. Participants inhaled Δ8-THC (10, 20, 40mg), Δ9-THC (20mg), or placebo (distilled water) using the Mighty Medic vaporizer. Measures included subjective drug effects, cognitive/psychomotor performance, puff topography, vital signs, and whole blood concentrations of Δ8-THC, Δ9-THC, and their metabolites.
All Δ8-THC doses and Δ9-THC produced subjective drug effects that differed from placebo. 20mg Δ9-THC elicited stronger ratings of “drug effect” and “unpleasant” than 10mg Δ8-THC; no other subjective effects differed between Δ8-THC and Δ9-THC. 20mg Δ9-THC impaired DRUID performance compared with placebo; no other significant differences were observed between conditions on cognitive/psychomotor measures. Few pharmacodynamic differences were observed between Δ8-THC doses. Evidence of compensatory puffing emerged, with longer/larger puffs at lower Δ8-THC doses and placebo. Blood cannabinoid concentrations revealed that Δ8-THC metabolism differed from Δ9-THC, with less psychoactive 11-OH metabolite formed after Δ8-THC exposure.
Various doses of vaporized Δ8-THC elicited comparable psychoactive effects as vaporized Δ9-THC, which is noteworthy considering Δ8-THC is less potent and generally perceived as less harmful/intoxicating than Δ9-THC. The magnitude of effects from cannabinoids is dictated by several factors including dose, route of administration, and, for inhaled methods, puffing behaviors. These data should be considered in future drug policy and public education initiatives.
•The prevalence of Δ8-tetrahydrocannabinol (Δ8-THC) has increased across the U.S.•Weevaluated the effects of vaporized Δ8-THC (10, 20, 40 mg) versus Δ9-THC (20mg) in healthy adults.•Vaporized Δ8-THC and Δ9-THC produced largely similar effects across all doses.•Participants altered their puffing behaviors based on Δ8-THC dose, indicative of titration.•Δ8-THC metabolism differed from Δ9-THC, as less psychoactive 11-OH metabolite was formed after Δ8-THC exposure The prevalence and accessibility of Δ8-tetrahydrocannabinol (Δ8-THC), a chemical isomer of Δ9-tetrahydrocannabinol (Δ9-THC), has increased drastically, yet no controlled studies have directly compared the effects of vaporized Δ8-THC and Δ9-THC . Twenty healthy adults with no past-month cannabis exposure completed five randomized outpatient sessions in a within-subjects, double-blind, crossover design. Participants inhaled Δ8-THC (10, 20, 40mg), Δ9-THC (20mg), or placebo (distilled water) using the Mighty Medic vaporizer. Measures included subjective drug effects, cognitive/psychomotor performance, puff topography, vital signs, and whole blood concentrations of Δ8-THC, Δ9-THC, and their metabolites. All Δ8-THC doses and Δ9-THC produced subjective drug effects that differed from placebo. 20mg Δ9-THC elicited stronger ratings of "drug effect" and "unpleasant" than 10mg Δ8-THC; no other subjective effects differed between Δ8-THC and Δ9-THC. 20mg Δ9-THC impaired DRUID performance compared with placebo; no other significant differences were observed between conditions on cognitive/psychomotor measures. Few pharmacodynamic differences were observed between Δ8-THC doses. Evidence of compensatory puffing emerged, with longer/larger puffs at lower Δ8-THC doses and placebo. Blood cannabinoid concentrations revealed that Δ8-THC metabolism differed from Δ9-THC, with less psychoactive 11-OH metabolite formed after Δ8-THC exposure. Various doses of vaporized Δ8-THC elicited comparable psychoactive effects as vaporized Δ9-THC, which is noteworthy considering Δ8-THC is less potent and generally perceived as less harmful/intoxicating than Δ9-THC. The magnitude of effects from cannabinoids is dictated by several factors including dose, route of administration, and, for inhaled methods, puffing behaviors. These data should be considered in future drug policy and public education initiatives. The prevalence and accessibility of Δ8-tetrahydrocannabinol (Δ8-THC), a chemical isomer of Δ9-tetrahydrocannabinol (Δ9-THC), has increased drastically, yet no controlled studies have directly compared the effects of vaporized Δ8-THC and Δ9-THC .BACKGROUNDThe prevalence and accessibility of Δ8-tetrahydrocannabinol (Δ8-THC), a chemical isomer of Δ9-tetrahydrocannabinol (Δ9-THC), has increased drastically, yet no controlled studies have directly compared the effects of vaporized Δ8-THC and Δ9-THC .Twenty healthy adults with no past-month cannabis exposure completed five randomized outpatient sessions in a within-subjects, double-blind, crossover design. Participants inhaled Δ8-THC (10, 20, 40mg), Δ9-THC (20mg), or placebo (distilled water) using the Mighty Medic vaporizer. Measures included subjective drug effects, cognitive/psychomotor performance, puff topography, vital signs, and whole blood concentrations of Δ8-THC, Δ9-THC, and their metabolites.METHODSTwenty healthy adults with no past-month cannabis exposure completed five randomized outpatient sessions in a within-subjects, double-blind, crossover design. Participants inhaled Δ8-THC (10, 20, 40mg), Δ9-THC (20mg), or placebo (distilled water) using the Mighty Medic vaporizer. Measures included subjective drug effects, cognitive/psychomotor performance, puff topography, vital signs, and whole blood concentrations of Δ8-THC, Δ9-THC, and their metabolites.All Δ8-THC doses and Δ9-THC produced subjective drug effects that differed from placebo. 20mg Δ9-THC elicited stronger ratings of "drug effect" and "unpleasant" than 10mg Δ8-THC; no other subjective effects differed between Δ8-THC and Δ9-THC. 20mg Δ9-THC impaired DRUID performance compared with placebo; no other significant differences were observed between conditions on cognitive/psychomotor measures. Few pharmacodynamic differences were observed between Δ8-THC doses. Evidence of compensatory puffing emerged, with longer/larger puffs at lower Δ8-THC doses and placebo. Blood cannabinoid concentrations revealed that Δ8-THC metabolism differed from Δ9-THC, with less psychoactive 11-OH metabolite formed after Δ8-THC exposure.RESULTSAll Δ8-THC doses and Δ9-THC produced subjective drug effects that differed from placebo. 20mg Δ9-THC elicited stronger ratings of "drug effect" and "unpleasant" than 10mg Δ8-THC; no other subjective effects differed between Δ8-THC and Δ9-THC. 20mg Δ9-THC impaired DRUID performance compared with placebo; no other significant differences were observed between conditions on cognitive/psychomotor measures. Few pharmacodynamic differences were observed between Δ8-THC doses. Evidence of compensatory puffing emerged, with longer/larger puffs at lower Δ8-THC doses and placebo. Blood cannabinoid concentrations revealed that Δ8-THC metabolism differed from Δ9-THC, with less psychoactive 11-OH metabolite formed after Δ8-THC exposure.Various doses of vaporized Δ8-THC elicited comparable psychoactive effects as vaporized Δ9-THC, which is noteworthy considering Δ8-THC is less potent and generally perceived as less harmful/intoxicating than Δ9-THC. The magnitude of effects from cannabinoids is dictated by several factors including dose, route of administration, and, for inhaled methods, puffing behaviors. These data should be considered in future drug policy and public education initiatives.CONCLUSIONVarious doses of vaporized Δ8-THC elicited comparable psychoactive effects as vaporized Δ9-THC, which is noteworthy considering Δ8-THC is less potent and generally perceived as less harmful/intoxicating than Δ9-THC. The magnitude of effects from cannabinoids is dictated by several factors including dose, route of administration, and, for inhaled methods, puffing behaviors. These data should be considered in future drug policy and public education initiatives. |
ArticleNumber | 112684 |
Author | Winecker, Ruth Hayes, Eugene Zamarripa, C. Austin Davis, Lisa S. Vandrey, Ryan Spindle, Tory R. Schriefer, Destiny Cone, Edward J. Kuntz, David Flegel, Ronald |
Author_xml | – sequence: 1 givenname: Tory R. orcidid: 0000-0002-2859-116X surname: Spindle fullname: Spindle, Tory R. email: tspindle@jhmi.edu organization: Behavioral Pharmacology Research Unit, Johns Hopkins University School of Medicine, Baltimore, USA – sequence: 2 givenname: C. Austin surname: Zamarripa fullname: Zamarripa, C. Austin organization: Behavioral Pharmacology Research Unit, Johns Hopkins University School of Medicine, Baltimore, USA – sequence: 3 givenname: Destiny orcidid: 0000-0003-3583-1659 surname: Schriefer fullname: Schriefer, Destiny organization: Behavioral Pharmacology Research Unit, Johns Hopkins University School of Medicine, Baltimore, USA – sequence: 4 givenname: Edward J. surname: Cone fullname: Cone, Edward J. organization: Behavioral Pharmacology Research Unit, Johns Hopkins University School of Medicine, Baltimore, USA – sequence: 5 givenname: Ruth surname: Winecker fullname: Winecker, Ruth organization: RTI International, Research Triangle Park, NC, USA – sequence: 6 givenname: Ronald surname: Flegel fullname: Flegel, Ronald organization: Substance Abuse and Mental Health Services Administration (SAMHSA), Division of Workplace Programs (DWP), Rockville, MD, USA – sequence: 7 givenname: Eugene surname: Hayes fullname: Hayes, Eugene organization: Substance Abuse and Mental Health Services Administration (SAMHSA), Division of Workplace Programs (DWP), Rockville, MD, USA – sequence: 8 givenname: Lisa S. surname: Davis fullname: Davis, Lisa S. organization: Substance Abuse and Mental Health Services Administration (SAMHSA), Division of Workplace Programs (DWP), Rockville, MD, USA – sequence: 9 givenname: David surname: Kuntz fullname: Kuntz, David organization: Clinical Reference Laboratory, Inc, USA – sequence: 10 givenname: Ryan surname: Vandrey fullname: Vandrey, Ryan organization: Behavioral Pharmacology Research Unit, Johns Hopkins University School of Medicine, Baltimore, USA |
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Keywords | Δ9-tetrahydrocannabinol Δ8-tetrahydrocannabinol Cannabinoids Δ8-THC Δ9-THC |
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SubjectTerms | Administration, Inhalation Adult Cannabinoids Cognition - drug effects Cross-Over Studies Dose-Response Relationship, Drug Double-Blind Method Dronabinol - administration & dosage Dronabinol - blood Dronabinol - pharmacology Female Healthy Volunteers Humans Male Psychomotor Performance - drug effects Young Adult Δ8-tetrahydrocannabinol Δ8-THC Δ9-tetrahydrocannabinol Δ9-THC |
Title | A within-subject cross-over trial comparing the acute effects of vaporized delta-8-tetrahydrocannabinol and delta-9-tetrahydrocannabinol in healthy adults |
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