Institute of Medical Science, University of Toronto, 1 King's College Circle, Toronto, Ontario M5S 1A8, Canada; Brain Health Imaging Centre, Centre for Addiction and Mental Health, 250 College Street, Toronto, Ontario M5T 1R8, Canada; Schulich School of Medicine and Dentistry, University of Western Ontario, 1151 Richmond Street, London, Ontario N6A 5C1, Canada.
Institute of Medical Science, University of Toronto, 1 King's College Circle, Toronto, Ontario M5S 1A8, Canada; Brain Health Imaging Centre, Centre for Addiction and Mental Health, 250 College Street, Toronto, Ontario M5T 1R8, Canada.
Neurosci Biobehav Rev. 2022 Jul;138:104680. doi: 10.1016/j.neubiorev.2022.104680. Epub 2022 May 2.
There is a clear link between psychiatric disorders and social behaviour, and evidence suggests the involvement of the endocannabinoid system (ECS). A systematic review of preclinical literature was conducted using MEDLINE (PubMed) and PsychINFO databases to examine whether pharmacological and/or genetic manipulations of the ECS alter social behaviours in wildtype (WT) animals or models of social impairment (SIM). Eighty studies were included. Risk of bias (RoB) was assessed using SYRCLE's RoB tool. While some variability was evident, studies most consistently found that direct cannabinoid receptor (CBR) agonism decreased social behaviours in WT animals, while indirect CBR activation via enzyme inhibition or gene-knockout increased social behaviours. Direct and, more consistently, indirect CBR activation reversed social deficits in SIM. These CBR-mediated effects were often sex- and developmental-phase-dependent and blocked by CBR antagonism. Overall, ECS enzyme inhibition may improve social behaviour in SIM, suggesting the potential usefulness of ECS enzyme inhibition as a therapeutic approach for social deficits. Future research should endeavour to elucidate ECS status in neuropsychiatric disorders characterized by social deficits.
精神疾病与社会行为之间存在明显的联系,有证据表明内源性大麻素系统(ECS)的参与。使用 MEDLINE(PubMed)和 PsychINFO 数据库对临床前文献进行了系统综述,以检查 ECS 的药理学和/或遗传操作是否改变野生型(WT)动物或社会障碍模型(SIM)中的社会行为。共纳入 80 项研究。使用 SYRCLE 的 RoB 工具评估偏倚风险(RoB)。虽然存在一些差异,但大多数研究一致发现,直接大麻素受体(CBR)激动剂降低 WT 动物的社会行为,而通过酶抑制或基因敲除间接激活 CBR 则增加社会行为。直接和更一致的间接 CBR 激活逆转了 SIM 中的社会缺陷。这些 CBR 介导的效应通常与性别和发育阶段有关,并被 CBR 拮抗作用阻断。总的来说,ECS 酶抑制可能改善 SIM 中的社会行为,表明 ECS 酶抑制作为治疗社会缺陷的潜在方法具有潜力。未来的研究应努力阐明以社会缺陷为特征的神经精神疾病中的 ECS 状态。