Chambers R Andrew, Bickel Warren K, Potenza Marc N
Lab for Translational Neuroscience of Dual Diagnosis & Development, Institute of Psychiatric Research, Indiana Division of Mental Health and Addiction, Indiana University School of Medicine, 791 Union Drive, Indianapolis, IN 46202, USA.
Neurosci Biobehav Rev. 2007;31(7):1017-45. doi: 10.1016/j.neubiorev.2007.04.005. Epub 2007 May 3.
Scale-free organizations, characterized by uneven distributions of linkages between nodal elements, describe the structure and function of many life-based complex systems developing under evolutionary pressures. We explore motivated behavior as a scale-free map toward a comprehensive translational theory of addiction. Motivational and behavioral repertoires are reframed as link and nodal element sets, respectively, comprising a scale-free structure. These sets are generated by semi-independent information-processing streams within cortical-striatal circuits that cooperatively provide decision-making and sequential processing functions necessary for traversing maps of motivational links connecting behavioral nodes. Dopamine modulation of cortical-striatal plasticity serves a central-hierarchical mechanism for survival-adaptive sculpting and development of motivational-behavioral repertoires by guiding a scale-free design. Drug-induced dopamine activity promotes drug taking as a highly connected behavioral hub at the expense of natural-adaptive motivational links and behavioral nodes. Conceptualizing addiction as pathological alteration of scale-free motivational-behavioral repertoires unifies neurobiological, neurocomputational and behavioral research while addressing addiction vulnerability in adolescence and psychiatric illness. This model may inform integrative research in defining more effective prevention and treatment strategies for addiction.
无标度组织以节点元素之间连接的不均匀分布为特征,描述了在进化压力下发展的许多基于生命的复杂系统的结构和功能。我们将动机行为探索为一种无标度图谱,以建立成瘾的全面转化理论。动机和行为库分别被重新定义为链接集和节点元素集,构成一种无标度结构。这些集合由皮质-纹状体回路内半独立的信息处理流生成,这些信息处理流协同提供遍历连接行为节点的动机链接图谱所需的决策和顺序处理功能。多巴胺对皮质-纹状体可塑性的调节通过引导无标度设计,为生存适应性塑造和动机-行为库的发展提供了一种核心层次机制。药物诱导的多巴胺活动促进药物摄取,使其成为一个高度连接的行为枢纽,却以自然适应性动机链接和行为节点为代价。将成瘾概念化为无标度动机-行为库的病理性改变,统一了神经生物学、神经计算和行为研究,同时解决了青少年成瘾易感性和精神疾病问题。该模型可能为定义更有效的成瘾预防和治疗策略的综合研究提供参考。