Hebert Francois-Olivier, Mongeau-Pérusse Violaine, Rizkallah Elie, Mahroug Amani, Bakouni Hamzah, Morissette Florence, Brissette Suzanne, Bruneau Julie, Dubreucq Simon, Jutras-Aswad Didier
Research Center, Centre Hospitalier de l'Université de Montréal (CRCHUM), Montréal, Canada.
Department of Psychiatry and Addiction, Faculty of Medicine, Université de Montréal, Montréal, Canada.
Cannabis Cannabinoid Res. 2025 Apr;10(2):e341-e352. doi: 10.1089/can.2023.0273. Epub 2024 May 21.
Cannabidiol (CBD) has been proposed to have a therapeutic potential over a wide range of neuropsychiatric disorders, including substance use disorders. Pre-clinical evidence suggests that CBD can increase anandamide (AEA) plasma concentration, possibly mediating some of its therapeutic properties. Whether CBD exerts such an effect on AEA in individuals with cocaine use disorder (CUD) remains unknown. To explore the sustained effects of daily CBD administration on AEA plasma concentrations compared with placebo in CUD. We used data from a randomized, double-blind, placebo-controlled trial evaluating CBD's efficacy in CUD. Seventy-eight individuals were randomized to receive a daily oral dose of 800 mg CBD ( = 40) or a placebo ( = 38). Participants stayed in an inpatient detoxification setting for 10 days, after which they were followed in an outpatient setting for 12 weeks. AEA plasma concentration was measured at baseline and at 23-h post CBD ingestion on day 8 and week 4. A generalized estimating equation model was used to assess CBD's effects on AEA, and sensitivity analyses were computed using Bayesian linear regressions. Sixty-four participants were included in the analysis. Similar mean AEA plasma concentrations in both treatment groups ( = 0.357) were observed. At day 8, mean AEA plasma concentrations (± standard deviation) were 0.26 (± 0.07) ng/mL in the CBD group and 0.29 (± 0.08) ng/mL in the placebo group ( = 0.832; Bayes factor [BF] = 0.190). At week 4, they were 0.27 (± 0.09) ng/mL in the CBD group and 0.30 (± 0.09) ng/mL in the placebo group ( = 0.181; BF = 0.194). While not excluding any potential acute and short-term effect, daily CBD administration did not exert a sustained impact on AEA plasma concentrations in individuals with CUD compared with placebo. clinicaltrials.gov (NCT02559167).
大麻二酚(CBD)已被认为在包括物质使用障碍在内的多种神经精神疾病中具有治疗潜力。临床前证据表明,CBD可提高花生四烯乙醇胺(AEA)的血浆浓度,这可能介导了其一些治疗特性。CBD对可卡因使用障碍(CUD)患者的AEA是否有这样的作用尚不清楚。为了探究与安慰剂相比,每日服用CBD对CUD患者AEA血浆浓度的持续影响。我们使用了一项评估CBD对CUD疗效的随机、双盲、安慰剂对照试验的数据。78名个体被随机分为每日口服800毫克CBD组(n = 40)或安慰剂组(n = 38)。参与者在住院戒毒环境中待10天,之后在门诊环境中随访12周。在基线、第8天和第4周CBD摄入后23小时测量AEA血浆浓度。使用广义估计方程模型评估CBD对AEA的影响,并使用贝叶斯线性回归进行敏感性分析。64名参与者纳入分析。两个治疗组的AEA血浆平均浓度相似(p = 0.357)。在第8天,CBD组的AEA血浆平均浓度(±标准差)为0.26(±0.07)纳克/毫升,安慰剂组为0.29(±0.08)纳克/毫升(p = 0.832;贝叶斯因子[BF] = 0.190)。在第4周,CBD组为0.27(±0.09)纳克/毫升,安慰剂组为0.30(±0.09)纳克/毫升(p = 0.181;BF = 0.194)。虽然不排除任何潜在的急性和短期影响,但与安慰剂相比,每日服用CBD对CUD患者的AEA血浆浓度没有持续影响。clinicaltrials.gov(NCT02559167)。