Kayir Hakan, Ruffolo Jessica, McCunn Patrick, Khokhar Jibran Y
Department of Biomedical Sciences, Ontario Veterinary College, University of Guelph, Guelph, ON, Canada.
Hotchkiss Brain Institute, Cumming School of Medicine, University of Calgary, Calgary, AB, Canada.
Curr Top Behav Neurosci. 2023;63:437-461. doi: 10.1007/7854_2022_396.
The consequences of cannabis use, especially in the context of schizophrenia, have gained increased importance with the legalization of cannabis in North America and across the globe. Cannabis use has multifaceted impacts on cognition in schizophrenia patients and healthy subjects. Healthy subjects, particularly those who initiated cannabis use at earlier ages and used high-potency cannabis for longer durations, exhibited poorer cognition mainly in working memory and attention. Cannabis use in schizophrenia has been associated with symptom exacerbation, longer and more frequent psychotic episodes, and poorer treatment outcomes. However, cannabis-using patients have better overall cognitive performance compared to patients who were not cannabis users. Interestingly, these effects were only apparent in lifetime cannabis users, but not in current (or within last 6 months) users. Moreover, higher frequency and earlier age of cannabis use initiation (i.e., before 17 years of age) were associated with better cognitive performance, although they had an earlier illness onset. Three possible hypotheses seem to come forward to explain this paradox. First, some components of cannabis may have antipsychotic or cognitive-enhancing properties. Secondly, chronic cannabis use may alter endocannabinoid signaling in the brain which could be a protective factor for developing psychosis or cognitive impairments. A third explanation could be their representation of a phenotypically distinct patient group with more intact cognitive functioning and less neurodevelopmental pathology. Multiple factors need to be considered to understand the complex relationship between cannabis, cognitive function, and schizophrenia. In short, age at initiation, duration and rate of cannabis use, abstinence duration, co-use of substances and alcohol, prescribed medications, relative cannabinoid composition and potency of cannabis, presence of genetic and environmental vulnerability factors are prominent contributors to the variability in outcomes. Animal studies support the disruptive effects of Δ9-tetrahydrocannabinol (THC) administration during adolescence on attention and memory performance. They provide insights about interaction of cannabinoid receptors with other neurotransmitter systems, such as GABA and glutamate, and other regulatory molecules, such as PSD95 and synaptophysin. Cannabidiol (CBD), on the other hand, can improve cognitive deficits seen in neurodevelopmental and chemically-induced animal models of schizophrenia. Future studies focusing on bridging the translational gaps between human and animal studies, through the use of translationally relevant methods of exposure (e.g., vaping), consistent behavioral assessments, and congruent circuit interrogations (e.g., imaging) will help to further clarify this complex picture.
随着大麻在北美及全球范围内的合法化,使用大麻的后果,尤其是在精神分裂症背景下的后果,变得愈发重要。大麻使用对精神分裂症患者和健康受试者的认知有多方面的影响。健康受试者,尤其是那些在较早年龄开始使用大麻且长期使用高效力大麻的人,主要在工作记忆和注意力方面表现出较差的认知能力。在精神分裂症患者中,使用大麻与症状加重、更长且更频繁的精神病发作以及更差的治疗结果相关。然而,与不使用大麻的患者相比,使用大麻的患者总体认知表现更好。有趣的是,这些影响仅在终生使用大麻的患者中明显,而在当前(或过去6个月内)使用者中不明显。此外,大麻使用起始频率更高和年龄更早(即17岁之前)与更好的认知表现相关,尽管他们发病更早。似乎有三种可能的假说来解释这一矛盾。首先,大麻的某些成分可能具有抗精神病或认知增强特性。其次,长期使用大麻可能会改变大脑中的内源性大麻素信号,这可能是预防精神病或认知障碍的保护因素。第三种解释可能是它们代表了一个表型上不同的患者群体,其认知功能更完整,神经发育病理学特征更少。需要考虑多个因素来理解大麻、认知功能和精神分裂症之间的复杂关系。简而言之,起始年龄、大麻使用的持续时间和频率、戒断时间、物质和酒精的共同使用、处方药、大麻的相对大麻素成分和效力、遗传和环境脆弱性因素的存在是结果变异性的主要影响因素。动物研究支持青春期给予Δ9-四氢大麻酚(THC)对注意力和记忆表现的破坏作用。它们提供了关于大麻素受体与其他神经递质系统(如γ-氨基丁酸和谷氨酸)以及其他调节分子(如突触后密度蛋白95和突触素)相互作用的见解。另一方面,大麻二酚(CBD)可以改善在神经发育和化学诱导的精神分裂症动物模型中看到的认知缺陷。未来的研究通过使用与转化相关的暴露方法(如雾化)、一致的行为评估和一致的神经回路研究(如图像检查)来弥合人类和动物研究之间的转化差距,将有助于进一步阐明这一复杂情况。