Effects of endocannabinoid system modulation on social behaviour: A systematic review of animal studies

被引:4
|
作者
Ahmed, Mashal [1 ,4 ,5 ]
Best, Laura M. [1 ,4 ]
Pereira, Christina F. [1 ,4 ]
Boileau, Isabelle [1 ,2 ,3 ,4 ]
Kloiber, Stefan [1 ,2 ,3 ,4 ]
机构
[1] Univ Toronto, Inst Med Sci, 1 Kings Coll Circle, Toronto, ON M5S 1A8, Canada
[2] Univ Toronto, Dept Psychiat, 250 Coll St, Toronto, ON M5T 1R8, Canada
[3] Campbell Family Mental Hlth Res Inst, Ctr Addict & Mental Hlth, 100 Stokes St, Toronto, ON M6J 1H4, Canada
[4] Brain Hlth Imaging Ctr, Ctr Addict & Mental Hlth, 250 Coll St, Toronto, ON M5T 1R8, Canada
[5] Univ Western Ontario, Schulich Sch Med & Dent, 1151 Richmond St, London, ON N6A 5C1, Canada
来源
基金
加拿大健康研究院;
关键词
Endocannabinoid system; Cannabinoid receptor drugs; Endocannabinoid metabolism inhibitors; Social behaviour; Social interaction; Social deficits; Animal models; Preclinical; ACID AMIDE HYDROLASE; CB1 RECEPTOR ANTAGONISM; ANXIETY-LIKE BEHAVIOR; PLAY-BEHAVIOR; CANNABIS USE; RAT MODEL; ADOLESCENT DELTA-9-TETRAHYDROCANNABINOL; GLUTAMATERGIC NEURONS; PREFRONTAL CORTEX; PRENATAL EXPOSURE;
D O I
10.1016/j.neubiorev.2022.104680
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
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.
引用
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页数:34
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