Psychopharmacology Research Unit, Discipline of Pharmacology, School of Biomedical Sciences, University of Western Australia, Perth, Western Australia, Australia.
Experimental and Regenerative Neurosciences, School of Biological Sciences, University of Western Australia, Crawley, Western Australia, Australia.
Cannabis Cannabinoid Res. 2024 Feb;9(1):199-211. doi: 10.1089/can.2022.0099. Epub 2022 Oct 5.
Memory impairments and psychosis-like experiences can be adverse effects of cannabis use. However, reports on the cognitive impact of cannabis use are not consistent. There are also limited studies on the psychotomimetic effects of cannabinoid compounds to reveal the association between cannabis and psychosis. Therefore, we investigated the effect of acute cannabinoid intoxication on verbal working memory (VWM) and spatial working memory (SWM) following oral doses of the synthetic cannabinoid agonist, nabilone (1-2 mg, oral). We further investigated the effect of nabilone on psychosis-like experiences (schizotypy scores) and associations of schizotypy with VWM and SWM. Healthy participants (=28) completed spatial and digit span tasks across different delay conditions (0, 6, 12, and 18 sec) after receiving nabilone (1-2 mg, PO) or placebo in a randomized, double-blind, counterbalanced, crossover manner. A subset of participants completed a short battery of schizotypy measures (=25). Nabilone impaired VWM (=0.03, weak effect size η=0.02) and SWM (=0.00016, η=0.08). Nabilone did not significantly change overall schizotypy scores. Schizotypy scores were negatively correlated with working memory (WM) averaged across all delays and both modalities, under placebo (=-0.41, =0.04). In addition, there were significant negative correlations between occasions of cannabis use and overall WM averaged scores across drug treatments (=-0.49, =0.007) and under placebo (=-0.45, =0.004). The results showed that the drug effect in the less frequent cannabis users was more pronounced on the SWM (<0.01) and VWM (<0.01), whereas there appeared to be little drug effect in the frequent cannabis users. Low doses of synthetic cannabinoid impaired SWM and VWM, indicating that exogenous activation of the cannabinoid system influences cognitive performance. Further, the results replicated previous findings that schizotypy is correlated with deficits in WM. Nabilone and caffeine effects on the perceptions of visually, auditory, tactile and multimodal illusions in healthy volunteers. CT-2018-CTN-02561 (Therapeutic Goods Administration Clinical Trial Registry) and ACTRN12618001292268 (The Australian New Zealand Clinical Trials Registry).
记忆损伤和类精神病体验可能是大麻使用的不良反应。然而,关于大麻使用的认知影响的报告并不一致。此外,关于大麻素化合物的致幻作用的研究也很有限,无法揭示大麻与精神病之间的关联。因此,我们研究了口服合成大麻素激动剂纳布隆(1-2mg)后急性大麻素中毒对言语工作记忆(VWM)和空间工作记忆(SWM)的影响。我们进一步研究了纳布隆对类精神病体验(精神分裂症评分)的影响,以及精神分裂症评分与 VWM 和 SWM 的关联。 健康参与者(=28)在接受纳布隆(1-2mg,PO)或安慰剂后,以随机、双盲、交叉、平衡的方式完成了不同延迟条件(0、6、12 和 18 秒)的空间和数字跨度任务。一小部分参与者完成了一组简短的精神分裂症评分测试(=25)。 纳布隆损害了 VWM(=0.03,弱效应大小 η=0.02)和 SWM(=0.00016,η=0.08)。纳布隆并未显著改变整体精神分裂症评分。在安慰剂下,精神分裂症评分与所有延迟和两种模式的平均工作记忆(WM)呈负相关(=-0.41,=0.04)。此外,在药物治疗和安慰剂下,大麻使用次数与平均总 WM 评分之间存在显著负相关(=-0.49,=0.007)和(=-0.45,=0.004)。结果表明,在较少使用大麻的人群中,药物对 SWM(<0.01)和 VWM(<0.01)的影响更为明显,而在经常使用大麻的人群中,药物的影响似乎很小。 低剂量合成大麻素损害了 SWM 和 VWM,表明外源性激活大麻素系统会影响认知表现。此外,结果复制了先前的发现,即精神分裂症与 WM 缺陷有关。 纳布隆和咖啡因对健康志愿者视觉、听觉、触觉和多模态错觉的感知影响。 CT-2018-CTN-02561(治疗用品管理局临床试验登记处)和 ACTRN12618001292268(澳大利亚和新西兰临床试验注册处)。