Alia-Klein Nelly, Goldstein Rita Z, Kriplani Aarti, Logan Jean, Tomasi Dardo, Williams Benjamin, Telang Frank, Shumay Elena, Biegon Anat, Craig Ian W, Henn Fritz, Wang Gene-Jack, Volkow Nora D, Fowler Joanna S
Medical Department, Brookhaven National Laboratory, Upton, New York 11973, USA.
J Neurosci. 2008 May 7;28(19):5099-104. doi: 10.1523/JNEUROSCI.0925-08.2008.
The genetic deletion of monoamine oxidase A (MAO A), an enzyme that breaks down the monoamine neurotransmitters norepinephrine, serotonin, and dopamine, produces aggressive phenotypes across species. Therefore, a common polymorphism in the MAO A gene (MAOA, Mendelian Inheritance in Men database number 309850, referred to as high or low based on transcription in non-neuronal cells) has been investigated in a number of externalizing behavioral and clinical phenotypes. These studies provide evidence linking the low MAOA genotype and violent behavior but only through interaction with severe environmental stressors during childhood. Here, we hypothesized that in healthy adult males the gene product of MAO A in the brain, rather than the gene per se, would be associated with regulating the concentration of brain amines involved in trait aggression. Brain MAO A activity was measured in vivo in healthy nonsmoking men with positron emission tomography using a radioligand specific for MAO A (clorgyline labeled with carbon 11). Trait aggression was measured with the multidimensional personality questionnaire (MPQ). Here we report for the first time that brain MAO A correlates inversely with the MPQ trait measure of aggression (but not with other personality traits) such that the lower the MAO A activity in cortical and subcortical brain regions, the higher the self-reported aggression (in both MAOA genotype groups) contributing to more than one-third of the variability. Because trait aggression is a measure used to predict antisocial behavior, these results underscore the relevance of MAO A as a neurochemical substrate of aberrant aggression.
单胺氧化酶A(MAO A)是一种分解单胺类神经递质去甲肾上腺素、血清素和多巴胺的酶,其基因缺失在跨物种中都会产生攻击性行为表型。因此,人们对MAO A基因中的一种常见多态性(MAOA,《人类孟德尔遗传数据库》编号309850,根据非神经细胞中的转录情况分为高或低)与多种外化行为和临床表型进行了研究。这些研究提供了证据,表明低MAOA基因型与暴力行为有关,但仅通过与童年时期的严重环境应激源相互作用才会如此。在此,我们假设,在健康成年男性中,大脑中的MAO A基因产物而非基因本身,会与调节参与特质性攻击行为的脑胺浓度有关。我们使用一种对MAO A具有特异性的放射性配体(用碳11标记的氯吉兰),通过正电子发射断层扫描在健康不吸烟男性体内测量脑MAO A活性。特质性攻击行为用多维人格问卷(MPQ)进行测量。我们首次报告,脑MAO A与MPQ攻击特质测量值呈负相关(但与其他人格特质无关),即皮质和皮质下脑区的MAO A活性越低,自我报告的攻击行为越高(在两个MAOA基因型组中都是如此),这一相关性对超过三分之一的变异性有贡献。由于特质性攻击行为是用于预测反社会行为的一种指标,这些结果强调了MAO A作为异常攻击行为的神经化学底物的相关性。