Chen Thomas J H, Blum Kenneth, Mathews Daniel, Fisher Larry, Schnautz Nancy, Braverman Eric R, Schoolfield John, Downs Bernard W, Comings David E
Chang Jung Christian University, Taiwan, ROC.
Med Hypotheses. 2005;65(4):703-7. doi: 10.1016/j.mehy.2005.04.037.
We hypothesize that pathological aggression, a complex behavioral disorder, in adolescents may in part involve polymorphisms of the dopaminergic system. While a number of neurotransmitter systems must be involved, due to polygenic inheritance, one major pathway should involve the dopaminergic system. Advances in our knowledge of the neurobiology of aggression and violence have given rise to rational pharmacological treatments for these behaviors. The main biological systems that are known to be involved are certain reward neurotransmitters including: serotonin, opioid peptides, gamma-aminobutyric acid, and the catecholamines (dopamine and norepinephrine). It is our notion that pathological aggressive behavior is in part similar mechanistically to other forms of impulsive behaviors such as pathological gambling. By analogy to drug dependence, it has been speculated that the underlying pathology in pathological gambling is a reduction in the sensitivity of the reward system. While studying pathological gamblers and controls during a guessing game using functional Magnetic Resonance Imaging, Reuter et al. observed a reduction of ventral striatal and ventromedial prefrontal activation in the pathological gamblers that were negatively correlated with gambling severity. Subsequently, linking hypo activation of these areas to disease severity. A positive correlation of both the dopamine D2 receptor gene (DRD2) and the dopamine transporter gene (DAT1) polymorphisms were observed with pathological violence in adolescents in a blinded clinical trial. Thus, this and other cited work preliminary suggest a role for both the DRD2 and DAT genes in pathological aggressive behavior. We further hypothesize that follow-up gene research in this area, albeit premature, resulting in confirmation of positive correlations with dopaminergic polymorphisms, and utilizing highly screened controls (eliminating any addictive, compulsive and impulsive behaviors in both proband and family) may have important ramifications in our young population.
我们推测,青少年的病理性攻击行为作为一种复杂的行为障碍,可能部分涉及多巴胺能系统的多态性。由于多基因遗传,虽然必然涉及多个神经递质系统,但一条主要途径应涉及多巴胺能系统。我们对攻击和暴力行为神经生物学认识的进展催生了针对这些行为的合理药物治疗方法。已知涉及的主要生物系统包括某些奖赏神经递质,如:血清素、阿片肽、γ-氨基丁酸以及儿茶酚胺(多巴胺和去甲肾上腺素)。我们认为,病理性攻击行为在机制上部分类似于其他形式的冲动行为,如病理性赌博。类比药物依赖,有人推测病理性赌博的潜在病理是奖赏系统敏感性降低。在一项使用功能磁共振成像的猜谜游戏中研究病理性赌博者和对照组时,罗伊特等人观察到病理性赌博者腹侧纹状体和腹内侧前额叶激活减少,且与赌博严重程度呈负相关。随后,将这些区域的低激活与疾病严重程度联系起来。在一项盲法临床试验中,观察到多巴胺D2受体基因(DRD2)和多巴胺转运体基因(DAT1)多态性与青少年病理性暴力行为均呈正相关。因此,这项研究及其他引用的工作初步表明DRD2和DAT基因在病理性攻击行为中发挥作用。我们进一步推测,尽管该领域的后续基因研究尚不成熟,但如果证实与多巴胺能多态性呈正相关,并使用经过高度筛选的对照组(排除先证者及其家族中的任何成瘾、强迫和冲动行为),可能会对我们的年轻人群产生重要影响。