Latzman Robert D, Schapiro Steven J, Hopkins William D
Department of Psychology, Georgia State UniversityAtlanta, GA, United States.
Michael E. Keeling Center for Comparative Medicine and Research, University of Texas MD Anderson Cancer CenterBastrop, TX, United States.
Front Neurosci. 2017 Jul 17;11:407. doi: 10.3389/fnins.2017.00407. eCollection 2017.
Vasopressin is a neuropeptide known to be associated with the development and evolution of complex socio-emotional behaviors including those relevant to psychopathic personality. In both humans and chimpanzees, recent research suggests a strong genetic contribution to individual variation in psychopathic traits. To date, however, little is known concerning specific genes that might explain the observed heritability of psychopathy. In a relatively large sample of captive chimpanzees ( = 164), the current study thus sought to investigate gene-environment associations between triarchic psychopathy dimensions (i.e., disinhibition, meanness, and boldness) and (1) early social rearing experiences and (2) polymorphisms in the promoter region of the V1A receptor gene (AVPR1A). Among chimpanzees raised by their biological conspecific mothers, AVPR1A was found to uniquely explain variability in disinhibition and in sex-specific ways for boldness and a total psychopathy score; however, in contrast, no significant associations were found between AVPR1A and any of the triarchic psychopathy dimensions in chimpanzees raised the first 3 years of life in a human nursery. Thus, when considered in its entirety, results suggest an important contributory influence of V1A receptor genotype variation in the explanation of the development of psychopathy under some but not all early rearing conditions. Results of the current study provide additional support for the assertion that psychopathic tendencies are rooted in basic, evolutionarily-meaningful dispositions, and provide support for a primate-translational operationalization of key neurobehavioral constructs relevant both to psychopathy and to broader forms of psychopathology.
血管加压素是一种神经肽,已知与复杂社会情感行为的发展和演变有关,包括与精神病态人格相关的行为。在人类和黑猩猩中,最近的研究表明,精神病态特征的个体差异有很强的遗传因素。然而,迄今为止,对于可能解释观察到的精神病态遗传性的特定基因知之甚少。因此,在一个相对较大的圈养黑猩猩样本(n = 164)中,本研究试图调查三元精神病态维度(即抑制不足、冷酷无情和大胆无畏)与(1)早期社会养育经历和(2)V1A受体基因(AVPR1A)启动子区域多态性之间的基因-环境关联。在由其亲生同种母亲抚养的黑猩猩中,发现AVPR1A能独特地解释抑制不足的变异性,以及在大胆无畏和总体精神病态得分方面的性别特异性变异;然而,相比之下,在人类托儿所度过生命最初3年的黑猩猩中,未发现AVPR1A与任何三元精神病态维度之间存在显著关联。因此,从整体上看,结果表明V1A受体基因型变异在某些但并非所有早期养育条件下对精神病态发展的解释中具有重要的促成影响。本研究结果为精神病态倾向植根于基本的、具有进化意义的性情这一论断提供了额外支持,并为与精神病态和更广泛形式的精神病理学相关的关键神经行为结构的灵长类动物转化操作化提供了支持。