Department of Psychiatry, UMC Utrecht Brain Center, University Medical Center Utrecht, Utrecht University, The Netherlands; Department of Translational Neuroscience, UMC Utrecht Brain Center, University Medical Center Utrecht, Utrecht University, The Netherlands.
Department of Psychiatry, UMC Utrecht Brain Center, University Medical Center Utrecht, Utrecht University, The Netherlands; Department of Psychiatry, Icahn School of Medicine at Mount Sinai, New York, USA.
Eur Neuropsychopharmacol. 2019 May;29(5):643-652. doi: 10.1016/j.euroneuro.2019.03.004. Epub 2019 Mar 15.
The relation of heavy cannabis use with decreased neuropsychological function has frequently been described but the underlying biological mechanisms are still largely unknown. This study investigates the relation of cannabis use with genome wide gene expression and subsequently examines the relations with neuropsychological function. Genome-wide gene expression in whole blood was compared between heavy cannabis users (N = 90) and cannabis naïve participants (N = 100) that were matched for psychotic like experiences. The results were validated using quantitative real-time PCR. Psychotic like experiences were assessed using the Comprehensive Assessment of Psychotic Experiences (CAPE). Neuropsychological function was estimated using four subtasks of the Wechsler Adult Intelligence Scale (WAIS). Subsequent in vitro studies in monocytes and a neuroblastoma cell line investigated expression changes in response to two major psychotropic components of cannabis; tetrahydrocannabinol (THC) and cannabidiol (CBD). mRNA expression of Protein Tyrosine Phosphatase Receptor Type F Polypeptide-Interacting-Protein Alpha-2 (PPFIA2) was significantly higher in cannabis users (LogFold Change 0.17) and confirmed by qPCR analysis. PPFIA2 expression level was negatively correlated with estimated intelligence (B=-22.9, p = 0.002) also in the 100 non-users (B=-28.5, p = 0.037). In vitro exposure of monocytes to CBD led to significant increase in PPFIA2 expression. However, exposure of monocytes to THC and neuroblastoma cells to THC or CBD did not change PPFIA2 expression. Change in PPFIA2 gene expression in response to cannabinoids is a putative mechanism by which cannabis could influence neuropsychological functions. The findings warrant further exploration of the role of PPFIA2 in cannabis induced changes of neuropsychological function, particularly in relation to CBD.
大麻使用与神经认知功能下降的关系经常被描述,但潜在的生物学机制仍知之甚少。本研究调查了大麻使用与全基因组基因表达的关系,随后检查了与神经认知功能的关系。比较了 90 名重度大麻使用者(N=90)和 100 名未使用大麻的参与者(N=100)的全血全基因组基因表达,这些参与者的精神病样体验相匹配。使用定量实时 PCR 验证了结果。使用综合精神病体验评估(CAPE)评估精神病样体验。使用韦氏成人智力量表(WAIS)的四个子任务估计神经认知功能。随后在单核细胞和神经母细胞瘤细胞系中的体外研究调查了两种大麻主要精神活性成分(四氢大麻酚(THC)和大麻二酚(CBD))对表达变化的影响。大麻使用者的蛋白酪氨酸磷酸酶受体 F 型多肽相互作用蛋白 Alpha-2(PPFIA2)的 mRNA 表达明显更高(LogFold Change 0.17),并通过 qPCR 分析得到证实。PPFIA2 表达水平与估计的智力呈负相关(B=-22.9,p=0.002),在 100 名非使用者中也是如此(B=-28.5,p=0.037)。体外暴露于 CBD 可导致 PPFIA2 表达显著增加。然而,暴露于 THC 的单核细胞和暴露于 THC 或 CBD 的神经母细胞瘤细胞均未改变 PPFIA2 表达。对大麻素的反应中 PPFIA2 基因表达的变化是大麻影响神经认知功能的一个潜在机制。这些发现证明了进一步研究 PPFIA2 在大麻引起的神经认知功能变化中的作用的必要性,特别是与 CBD 相关的作用。