4.5 Article

Sex differences in the subjective effects of oral Δ9-THC in cannabis users

Journal

PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR
Volume 152, Issue -, Pages 44-51

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.pbb.2016.01.007

Keywords

Marijuana; Cannabis; Gender; Drug-discrimination; Self-report

Funding

  1. National Institute on Drug Abuse [NIDA] [K01 DA018772, K02 DA031766, R01 DA025605, R01 DA036550]
  2. NIDA T32 training grant [DA035200]
  3. National Center for Advancing Translational Sciences [UL1TR000117]

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Previous studies suggest that there are sex differences in endocannabinoid function and the response to exogenous cannabinoids, though data from clinical studies comparing acute cannabinoid effects in men and women under controlled laboratory conditions are limited. To further explore these potential differences, data from 30 cannabis users (N = 18 M, 12 F) who completed previous g-tetrahydrocannabinol (Delta(9)-THC) discrimination studies were combined for this retrospective analysis. In each study, subjects learned to discriminate between oral Delta(9)-THC and placebo and then received a range of Delta(9)-THC doses (0, 5,15 and a high dose of either 25 or 30 mg). Responses on a drug-discrimination task, subjective effects questionnaire, psychomotor performance tasks, and physiological measures were assessed. Delta(9)-THC dose-dependently increased drug-appropriate responding, ratings on positive Visual Analog Scale (VAS) items (e.g., good effects, like drug, take again), and items related to intoxication (e.g., high, stoned). Delta(9)-THC also dose-dependently impaired performance on psychomotor tasks and elevated heart rate. Sex differences on VAS items emerged as a function of dose. Women exhibited significantly greater subjective responses to oral drug administration than men at the 5 mg Delta(9)-THC dose, whereas men were more sensitive to the subjective effects of the 15 mg dose of Delta(9)-THC than women. These results demonstrate dose-dependent separation in the subjective response to oral Delta(9)-THC administration by sex, which might contribute to the differential development of problematic cannabis use. (C) 2016 Elsevier Inc. All rights reserved.

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