Department of Psychology, University of Tartu, Estonian Centre of Behavioural and Health Sciences, Tiigi 78, 50410 Tartu, Estonia.
Pharmacol Ther. 2010 Mar;125(3):402-22. doi: 10.1016/j.pharmthera.2009.11.006. Epub 2009 Dec 21.
Susceptibility to affective disorders is individually different, and determined both by genetic variance and life events that cause significant differences in the CNS structure and function between individual subjects. Therefore it is plausible that search for the inter-individual differences in endophenotypes that mediate the effects of causal factors, both genetic and environmental, will reveal the substrates for vulnerability, help to clarify pathogenetic mechanisms, and possibly aid in developing strategies to discover better, more personalized treatments. This review first examines comparatively a number of animal models of human affect and affect-related disorders that rely on persistent inter-individual differences, and then highlights some of the neurobiological findings in these models that are compatible with much of research in human behavioural and personality traits. Many behaviours occur in specific combinations in several models, but often remarkable dissociations are observed, providing a variety of constellations of traits. It is concluded that more systematic comparative experimentation on behaviour and neurobiology in different models is warranted to reveal possible "building blocks" of affect-related personality common in animals and humans. Looking into the perspectives in psychopharmacology the focus is placed on probable associations of inter-individual differences with brain structure and function, personality and coping strategies, and psychiatric vulnerability, highlighting some unexpected interactions between vulnerability endophenotypes, adverse life events, and behavioural traits. It is argued that further studies on inter-individual differences in affect and underlying neurobiology should include formal modeling of their epistatic, hierarchical and dynamic nature.
个体易感性差异决定了情感障碍的易感性,这种差异既受遗传变异的影响,也受导致个体中枢神经系统结构和功能显著差异的生活事件的影响。因此,寻找介导遗传和环境因素因果效应的个体差异内表型,可能会揭示易感性的基础,有助于阐明发病机制,并可能有助于制定发现更好、更个性化治疗方法的策略。这篇综述首先比较了几种依赖于持续个体差异的人类情感和情感相关障碍的动物模型,然后强调了这些模型中的一些神经生物学发现,这些发现与人类行为和人格特征的许多研究相吻合。许多行为在几种模型中以特定的组合出现,但通常会观察到显著的差异,从而提供了各种特征的组合。结论是,需要对不同模型中的行为和神经生物学进行更系统的比较实验,以揭示动物和人类中常见的与情感相关的人格的可能“构建块”。在精神药理学方面,重点关注个体差异与大脑结构和功能、人格和应对策略以及精神易感性之间的可能关联,强调了易感性内表型、不良生活事件和行为特征之间一些意想不到的相互作用。有人认为,进一步研究情感和潜在神经生物学的个体差异,应包括对其上位性、层次性和动态性质的正式建模。