Kolla Nathan J, Mishra Achal
Department of Forensic Psychiatry, Centre for Addiction and Mental Health, Toronto, ON, Canada.
Department of Psychiatry, Faculty of Medicine, University of Toronto, Toronto, ON, Canada.
Front Behav Neurosci. 2018 Mar 27;12:41. doi: 10.3389/fnbeh.2018.00041. eCollection 2018.
Endogenous and exogenous cannabinoids bind to central cannabinoid receptors to control a multitude of behavioral functions, including aggression. The first main objective of this review is to dissect components of the endocannabinoid system, including cannabinoid 1 and cannabinoid 2 receptors; the endogenous cannabinoids anandamide and 2-arachidonoylglycerol; and the indirect cannabinoid modulators fatty acid amide hydrolase and monoacylglycerol lipase; that have shown abnormalities in basic research studies investigating mechanisms of aggression. While most human research has concluded that the active ingredient of marijuana, Δ9-tetrahydrocannabinol, tends to dampen rather than provoke aggression in acute doses, recent evidence supports a relationship between the ingestion of synthetic cannabinoids and emergence of violent or aggressive behavior. Thus, another objective is to evaluate the emerging clinical data. This paper also discusses the relationship between prenatal and perinatal exposure to cannabis as well as use of cannabis in adolescence on aggressive outcomes. A final objective of the paper is to discuss endocannabinoid abnormalities in psychotic and affective disorders, as well as clinically aggressive populations, such as borderline personality disorder and antisocial personality disorder. With regard to the former condition, decreased anandamide metabolites have been reported in the cerebrospinal fluid, while some preliminary evidence suggests that fatty acid amide hydrolase genetic polymorphisms are linked to antisocial personality disorder and impulsive-antisocial psychopathic traits. To summarize, this paper will draw upon basic and clinical research to explain how the endocannabinoid system may contribute to the genesis of aggressive behavior.
内源性和外源性大麻素与中枢大麻素受体结合,以控制包括攻击行为在内的多种行为功能。本综述的首要主要目标是剖析内源性大麻素系统的组成部分,包括大麻素1和大麻素2受体;内源性大麻素花生四烯乙醇胺和2-花生四烯酸甘油酯;以及间接大麻素调节剂脂肪酸酰胺水解酶和单酰甘油脂肪酶;这些在研究攻击行为机制的基础研究中已显示出异常。虽然大多数人体研究得出结论,大麻的活性成分Δ9-四氢大麻酚在急性剂量下往往会抑制而非引发攻击行为,但最近的证据支持合成大麻素的摄入与暴力或攻击行为的出现之间存在关联。因此,另一个目标是评估新出现的临床数据。本文还讨论了产前和围产期接触大麻以及青少年使用大麻与攻击行为结果之间的关系。本文的最后一个目标是讨论精神病性和情感性障碍以及临床上具有攻击性的人群,如边缘型人格障碍和反社会人格障碍中的内源性大麻素异常。关于前一种情况,脑脊液中已报告花生四烯乙醇胺代谢物减少,而一些初步证据表明脂肪酸酰胺水解酶基因多态性与反社会人格障碍和冲动反社会精神病性特征有关。总之,本文将借鉴基础研究和临床研究来解释内源性大麻素系统如何可能促成攻击行为的发生。