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剖析冲动性及其与毒瘾的关系。

Dissecting impulsivity and its relationships to drug addictions.

机构信息

Department of Psychology, University of California Los Angeles, Los Angeles, California.

出版信息

Ann N Y Acad Sci. 2014 Oct;1327:1-26. doi: 10.1111/nyas.12388. Epub 2014 Mar 21.

Abstract

Addictions are often characterized as forms of impulsive behavior. That said, it is often noted that impulsivity is a multidimensional construct, spanning several psychological domains. This review describes the relationship between varieties of impulsivity and addiction-related behaviors, the nature of the causal relationship between the two, and the underlying neurobiological mechanisms that promote impulsive behaviors. We conclude that the available data strongly support the notion that impulsivity is both a risk factor for, and a consequence of, drug and alcohol consumption. While the evidence indicating that subtypes of impulsive behavior are uniquely informative--either biologically or with respect to their relationships to addictions--is convincing, multiple lines of study link distinct subtypes of impulsivity to low dopamine D2 receptor function and perturbed serotonergic transmission, revealing shared mechanisms between the subtypes. Therefore, a common biological framework involving monoaminergic transmitters in key frontostriatal circuits may link multiple forms of impulsivity to drug self-administration and addiction-related behaviors. Further dissection of these relationships is needed before the next phase of genetic and genomic discovery will be able to reveal the biological sources of the vulnerability for addiction indexed by impulsivity.

摘要

成瘾通常被描述为冲动行为的一种形式。也就是说,人们经常注意到,冲动是一个多维度的结构,涵盖了几个心理领域。本综述描述了各种冲动性与成瘾相关行为之间的关系,两者之间因果关系的本质,以及促进冲动行为的潜在神经生物学机制。我们得出的结论是,现有数据强烈支持这样一种观点,即冲动既是药物和酒精消费的风险因素,也是其后果。虽然有证据表明,冲动的亚型在生物学或与成瘾的关系方面具有独特的信息价值,但多项研究将不同的冲动亚型与多巴胺 D2 受体功能降低和 5-羟色胺传递功能障碍联系起来,揭示了亚型之间的共同机制。因此,涉及关键额纹体回路中单胺能递质的共同生物学框架可能将多种形式的冲动与药物自我给药和成瘾相关行为联系起来。在遗传和基因组发现的下一阶段能够揭示冲动所标记的成瘾易感性的生物学来源之前,需要进一步剖析这些关系。

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